Pathological pattern

Pathological pattern
Beskrivning

Pathological pattern

Date of assessment
Beskrivning

pp_date

Datatyp

date

Any proof of malignancy?     Please specify in comorbidities
Beskrivning

pp_proof_malign

Datatyp

integer

Underlying material for histopathological evaluation
Beskrivning

pp_material_evalu

Datatyp

text

Lymph node station right: 1. Supraclavicular
Beskrivning

pp_lymphstatright_1. Supraclavicular

Datatyp

integer

2. Upper tracheal
Beskrivning

pp_lymphstatright_2. Upper tracheal

Datatyp

integer

3. Prevascular
Beskrivning

pp_lymphstatright_3. Prevascular

Datatyp

integer

4. Lower paratracheal
Beskrivning

pp_lymphstatright_4. Lower paratracheal

Datatyp

integer

5. Subaortic
Beskrivning

pp_lymphstatright_5. Subaortic

Datatyp

integer

6. AP window
Beskrivning

pp_lymphstatright_6. AP window

Datatyp

integer

7. Subcarinal
Beskrivning

pp_lymphstatright_7. Subcarinal

Datatyp

integer

8. Paraesophagheal
Beskrivning

pp_lymphstatright_8. Paraesophagheal

Datatyp

integer

9. Pulmonary ligament
Beskrivning

pp_lymphstatright_9. Pulmonary ligament

Datatyp

integer

10. Hilar
Beskrivning

pp_lymphstatright_10. Hilar

Datatyp

integer

11. Interlobar
Beskrivning

pp_lymphstatright_11. Interlobar

Datatyp

integer

12. Lobar
Beskrivning

pp_lymphstatright_12. Lobar

Datatyp

integer

Lymph node station left: 1. Supraclavicular
Beskrivning

pp_lymphstatleft_1. Supraclavicular

Datatyp

integer

2. Upper tracheal
Beskrivning

pp_lymphstatleft_2. Upper tracheal

Datatyp

integer

3. Prevascular
Beskrivning

pp_lymphstatleft_3. Prevascular

Datatyp

integer

4. Lower paratracheal
Beskrivning

pp_lymphstatleft_4. Lower paratracheal

Datatyp

integer

5. Subaortic
Beskrivning

pp_lymphstatleft_5. Subaortic

Datatyp

integer

6. AP window
Beskrivning

pp_lymphstatleft_6. AP window

Datatyp

integer

7. Subcarinal
Beskrivning

pp_lymphstatleft_7. Subcarinal

Datatyp

integer

8. Paraesophagheal
Beskrivning

pp_lymphstatleft_8. Paraesophagheal

Datatyp

integer

9. Pulmonary ligament
Beskrivning

pp_lymphstatleft_9. Pulmonary ligament

Datatyp

integer

10. Hilar
Beskrivning

pp_lymphstatleft_10. Hilar

Datatyp

integer

11. Interlobar
Beskrivning

pp_lymphstatleft_11. Interlobar

Datatyp

integer

12. Lobar
Beskrivning

pp_lymphstatleft_12. Lobar

Datatyp

integer

Location biopsy upper lobe right: 1. Apical
Beskrivning

pp_biopsy_rightul_1. Apical

Datatyp

integer

2. Posterior
Beskrivning

pp_biopsy_rightul_2. Posterior

Datatyp

integer

3. Anterior
Beskrivning

pp_biopsy_rightul_3. Anterior

Datatyp

integer

Location biopsy middle lobe right: 4. Lateral
Beskrivning

pp_biopsy_rightml_4. Lateral

Datatyp

integer

5. Medial
Beskrivning

pp_biopsy_rightml_5. Medial

Datatyp

integer

Location biopsy lower lobe right: 6. Superior
Beskrivning

pp_biopsy_rightll_6. Superior

Datatyp

integer

7. Med. basal
Beskrivning

pp_biopsy_rightll_7. Med. basal

Datatyp

integer

8. Lat. basal
Beskrivning

pp_biopsy_rightll_8. Lat. basal

Datatyp

integer

9. Lat. basal
Beskrivning

pp_biopsy_rightll_9. Lat. basal

Datatyp

integer

10. Post basal
Beskrivning

pp_biopsy_rightll_10. Post basal

Datatyp

integer

Location biopsy upper lobe left: 1-2 Apical posterior
Beskrivning

pp_biopsy_leftul_1-2 Apical posterior

Datatyp

integer

3. Anterior
Beskrivning

pp_biopsy_leftul_3. Anterior

Datatyp

integer

4. Superior (Lingula)
Beskrivning

pp_biopsy_leftul_4. Superior (Lingula)

Datatyp

integer

5. Inferior (Lingula)
Beskrivning

pp_biopsy_leftul_5. Inferior (Lingula)

Datatyp

integer

Location biopsy lower lobe left: 6. Superior
Beskrivning

pp_biopsy_leftll_6. Superior

Datatyp

integer

7-8. Ant. basal
Beskrivning

pp_biopsy_leftll_7-8. Ant. basal

Datatyp

integer

9. Lat. basal
Beskrivning

pp_biopsy_leftll_9. Lat. basal

Datatyp

integer

10. Post. basal
Beskrivning

pp_biopsy_leftll_10. Post. basal

Datatyp

integer

Pathological patterns
Beskrivning

Pathological patterns

IIP patterns (as based on most recent ATS/ERS guidelines)
Beskrivning

pp_iippattern

Datatyp

integer

pathological_pattern.pp_patho_category___uip
Beskrivning

pathological_pattern.pp_patho_category___uip

IIP patterns UIP
Beskrivning

pp_patho_category_UIP

Datatyp

integer

NSIP
Beskrivning

pp_patho_category_NSIP

Datatyp

integer

AIP
Beskrivning

pp_patho_category_AIP

Datatyp

integer

OP
Beskrivning

pp_patho_category_OP

Datatyp

integer

RB-ILD
Beskrivning

pp_patho_category_RB-ILD

Datatyp

integer

DIP
Beskrivning

pp_patho_category_DIP

Datatyp

integer

LIP
Beskrivning

pp_patho_category_LIP

Datatyp

integer

PPFE
Beskrivning

pp_patho_category_PPFE

Datatyp

integer

AFOP
Beskrivning

pp_patho_category_AFOP

Datatyp

integer

BPIP
Beskrivning

pp_patho_category_BPIP

Datatyp

integer

ACIF
Beskrivning

pp_patho_category_ACIF

Datatyp

integer

UIP criteria Choose from drop down: definite, probable, indeterminate Dense fibrosis with architectural distortion
Beskrivning

pp_uippattern_Dense fibrosis with architectural distortion

Datatyp

integer

Predominant subpleural and/or paraseptal distribution of fibrosis
Beskrivning

pp_uippattern_Predominant subpleural and/or paraseptal distribution of fibrosis

Datatyp

integer

Patchy involvement of lung parenchyma by fibrosis
Beskrivning

pp_uippattern_Patchy involvement of lung parenchyma by fibrosis

Datatyp

integer

Fibroblast foci
Beskrivning

pp_uippattern_Fibroblast foci

Datatyp

integer

Honeycombing
Beskrivning

pp_uippattern_Honeycombing

Datatyp

integer

Absence of features suggesting an alternate diagnosis
Beskrivning

pp_uippattern_Absence of features suggesting an alternate diagnosis

Datatyp

integer

Some histologic features from def. UIP
Beskrivning

pp_uippattern_Some histologic features from def. UIP

Datatyp

integer

Fibrosis with or without architectural distortion
Beskrivning

pp_uippattern_Fibrosis with or without architectural distortion

Datatyp

integer

Please choose:
Beskrivning

pp_uip_subgroup

Datatyp

text

Suggested diagnosis: Definite UIP criteria
Beskrivning

pp_uip_definite

Datatyp

text

Suggested diagnosis: Probable UIP criteria
Beskrivning

pp_uip_probable

Datatyp

text

Suggested diagnosis: Indeterminate UIP criteria
Beskrivning

pp_uip_indeterminate

Datatyp

text

NSIP - Cellular
Beskrivning

pp_nsip_cellular

Datatyp

integer

Cellular interstitial pneumonia; lymphocytic or plasmacytic
Beskrivning

pp_nsip_subcell_Cellular interstitial pneumonia; lymphocytic or plasmacytic

Datatyp

integer

Diffuse and uniform inflammation ("temporal homogeneity")
Beskrivning

pp_nsip_subcell_Diffuse and uniform inflammation ("temporal homogeneity")

Datatyp

integer

Loose interstitial fibrosis
Beskrivning

pp_nsip_subcell_Loose interstitial fibrosis

Datatyp

integer

Preserved architecture
Beskrivning

pp_nsip_subcell_Preserved architecture

Datatyp

integer

NSIP - Fibrotic
Beskrivning

pp_nsip_fibrotic

Datatyp

integer

Depletion of inflammatory cells
Beskrivning

pp_nsip_subfibr_Depletion of inflammatory cells

Datatyp

integer

Dense fiber-rich interstitial fibrosis
Beskrivning

pp_nsip_subfibr_Dense fiber-rich interstitial fibrosis

Datatyp

integer

Preserved architecture
Beskrivning

pp_nsip_subfibr_Preserved architecture

Datatyp

integer

AIP - diffuse alveolar damage, almost completely identical to acute respiratory distress syndrome / diffuse alveolar damage morphologically
Beskrivning

pp_aip_discription

Datatyp

text

AIP - Exudative phase
Beskrivning

pp_aip_exudative

Datatyp

integer

Hyaline membranes in alveolar duct or sacs; scattered or not apparent
Beskrivning

pp_aip_subexudative_Hyaline membranes in alveolar duct or sacs; scattered or not apparent

Datatyp

integer

Interstitial and intra-alveolar edema
Beskrivning

pp_aip_subexudative_Interstitial and intra-alveolar edema

Datatyp

integer

Collapsed alveoli
Beskrivning

pp_aip_subexudative_Collapsed alveoli

Datatyp

integer

Denudation and necrosis of type I pneumocytes
Beskrivning

pp_aip_subexudative_Denudation and necrosis of type I pneumocytes

Datatyp

integer

Hemorrhage - usually mild
Beskrivning

pp_aip_subexudative_Hemorrhage - usually mild

Datatyp

integer

AIP - Proliferative / organizing phase
Beskrivning

pp_aip_proliferative

Datatyp

integer

Organizing pneumonia with / without remnants of hyaline membrane
Beskrivning

pp_aip_subproliferation_Organizing pneumonia with / without remnants of hyaline membrane

Datatyp

integer

Interstitial and intra-alveolar proliferation of fibroblasts / myofibroblasts
Beskrivning

pp_aip_subproliferation_Interstitial and intra-alveolar proliferation of fibroblasts / myofibroblasts

Datatyp

integer

Lymphocytic infiltration; usually more prominent than in acute respiratory distress syndrome
Beskrivning

pp_aip_subproliferation_Lymphocytic infiltration; usually more prominent than in acute respiratory distress syndrome

Datatyp

integer

Proliferation of type II pneumocytes with occasional cellular atypia
Beskrivning

pp_aip_subproliferation_Proliferation of type II pneumocytes with occasional cellular atypia

Datatyp

integer

Endothelial injury and fibrinous thromboembolism in arterioles / arteries
Beskrivning

pp_aip_subproliferation_Endothelial injury and fibrinous thromboembolism in arterioles / arteries

Datatyp

integer

AIP - Fibrosis phase
Beskrivning

pp_aip_fibrosis

Datatyp

integer

Diffuse collagenous fibrosis
Beskrivning

pp_aip_subfibrosis_Diffuse collagenous fibrosis

Datatyp

integer

Microscopic honeycomb-like change
Beskrivning

pp_aip_subfibrosis_Microscopic honeycomb-like change

Datatyp

integer

Traction bronchiolectasis
Beskrivning

pp_aip_subfibrosis_Traction bronchiolectasis

Datatyp

integer

Squamous metaplasia
Beskrivning

pp_aip_subfibrosis_Squamous metaplasia

Datatyp

integer

Organized thrombus
Beskrivning

pp_aip_subfibrosis_Organized thrombus

Datatyp

integer

Thickening of pleura with dilatation of lymphatic / blood vessels
Beskrivning

pp_aip_subfibrosis_Thickening of pleura with dilatation of lymphatic / blood vessels

Datatyp

integer

OP Fibroblastic plugs in alveolar sacs and ducts (organizing pneumonia) and bronchiolar lumen (bronchiolitis obliterans)
Beskrivning

pp_op_Fibroblastic plugs in alveolar sacs and ducts (organizing pneumonia) and bronchiolar lumen (bronchiolitis obliterans)

Datatyp

integer

Formed by spindled fibroblasts in pale staining matrix of immature loose collagen with polypoid shape (Masson body) or serpiginous or elongated form
Beskrivning

pp_op_Formed by spindled fibroblasts in pale staining matrix of immature loose collagen with polypoid shape (Masson body) or serpiginous or elongated form

Datatyp

integer

Organizing pneumonia sometimes extends from one alveolus to the next one through interalveolar fenestrae (butterfly pattern)
Beskrivning

pp_op_Organizing pneumonia sometimes extends from one alveolus to the next one through interalveolar fenestrae (butterfly pattern)

Datatyp

integer

Thickened alveolar septa with lymphocytes
Beskrivning

pp_op_Thickened alveolar septa with lymphocytes

Datatyp

integer

Alveolar architecture is usually preserved in cryptogenic organizing pneumonia
Beskrivning

pp_op_Alveolar architecture is usually preserved in cryptogenic organizing pneumonia

Datatyp

integer

Foamy macrophage accumulation in surrounding airspace may be present
Beskrivning

pp_op_Foamy macrophage accumulation in surrounding airspace may be present

Datatyp

integer

RB-ILD Lightly pigmented (smoker's) macrophages limited to distal airspaces and peribronchiolar airspaces
Beskrivning

pp_rbild_Lightly pigmented (smoker's) macrophages limited to distal airspaces and peribronchiolar airspaces

Datatyp

integer

Pigment within macrophage cytoplasm is yellow to light brown and finely granular
Beskrivning

pp_rbild_Pigment within macrophage cytoplasm is yellow to light brown and finely granular

Datatyp

integer

Minimal to absent peribronchiolar interstitial thickening by fibrosis
Beskrivning

pp_rbild_Minimal to absent peribronchiolar interstitial thickening by fibrosis

Datatyp

integer

No diffuse interstitial fibrosis or inflammation
Beskrivning

pp_rbild_No diffuse interstitial fibrosis or inflammation

Datatyp

integer

DIP Diffuse and massive accumulation of intra-alveolar macrophages (smoker's macrophages)
Beskrivning

pp_dip_Diffuse and massive accumulation of intra-alveolar macrophages (smoker's macrophages)

Datatyp

integer

Brown pigments
Beskrivning

pp_dip_Brown pigments

Datatyp

integer

Giant cells can be also seen
Beskrivning

pp_dip_Giant cells can be also seen

Datatyp

integer

Diffuse and homogeneous involvement (similar to NSIP) along with alveolar macrophages
Beskrivning

pp_dip_Diffuse and homogeneous involvement (similar to NSIP) along with alveolar macrophages

Datatyp

integer

Lymphoid follicles and eosinophils are often present
Beskrivning

pp_dip_Lymphoid follicles and eosinophils are often present

Datatyp

integer

LIP Lymphoid follicles with germinal centers
Beskrivning

pp_lip_Lymphoid follicles with germinal centers

Datatyp

integer

Bronchovascular bundles and interlobular septa are usually involved
Beskrivning

pp_lip_Bronchovascular bundles and interlobular septa are usually involved

Datatyp

integer

Alveolar structure is often inflated and disrupted
Beskrivning

pp_lip_Alveolar structure is often inflated and disrupted

Datatyp

integer

Typically CD8+ or CD4+ T cells or B cells predominate
Beskrivning

pp_lip_Typically CD8+ or CD4+ T cells or B cells predominate

Datatyp

integer

Interstitial or intra-alveolar giant cells
Beskrivning

pp_lip_Interstitial or intra-alveolar giant cells

Datatyp

integer

Intra-alveolar macrophages
Beskrivning

pp_lip_Intra-alveolar macrophages

Datatyp

integer

Type II pneumocyte hyperplasia
Beskrivning

pp_lip_Type II pneumocyte hyperplasia

Datatyp

integer

Cyst formation without marked fibrosis
Beskrivning

pp_lip_Cyst formation without marked fibrosis

Datatyp

integer

PPFE Linear subpleural elastofibrosis
Beskrivning

pp_ppfe_Linear subpleural elastofibrosis

Datatyp

integer

Onset in upper lung
Beskrivning

pp_ppfe_Onset in upper lung

Datatyp

integer

May be associated to UIP pattern in lower lung parts
Beskrivning

pp_ppfe_May be associated to UIP pattern in lower lung parts

Datatyp

integer

AFOP Dominant findings of intra-alveolar fibrin
Beskrivning

pp_afop_Dominant findings of intra-alveolar fibrin

Datatyp

integer

Involves more than 20% of the alveolar spaces in the lesion
Beskrivning

pp_afop_Involves more than 20% of the alveolar spaces in the lesion

Datatyp

integer

Neutrophils are usually scanty or absent
Beskrivning

pp_afop_Neutrophils are usually scanty or absent

Datatyp

integer

Organizing pneumonia: fibroblastic plugs in alveolar sacs and ducts with loose collagen matrix
Beskrivning

pp_afop_Organizing pneumonia: fibroblastic plugs in alveolar sacs and ducts with loose collagen matrix

Datatyp

integer

Diffuse and patchy distribution
Beskrivning

pp_afop_Diffuse and patchy distribution

Datatyp

integer

BPIP Peribronchiolar metaplasia
Beskrivning

pp_bpip_Peribronchiolar metaplasia

Datatyp

integer

Peribronchiolar fibrosis with preserved architecture
Beskrivning

pp_bpip_Peribronchiolar fibrosis with preserved architecture

Datatyp

integer

Under discussion
Beskrivning

pp_bpip_Under discussion

Datatyp

integer

ACIF
Beskrivning

pp_acif

Datatyp

integer

Langerhans Cell Histiocytosis (LCH)
Beskrivning

pp_lch

Datatyp

integer

Accumulation of activated LCs organised into loose
Beskrivning

pp_sublch_Accumulation of activated LCs organised into loose

Datatyp

integer

Infiltration with Lymphocytes and other inflammatory cells
Beskrivning

pp_sublch_Infiltration with Lymphocytes and other inflammatory cells

Datatyp

integer

Abundance of pigmented macrophages
Beskrivning

pp_sublch_Abundance of pigmented macrophages

Datatyp

integer

Granulomateous patterns
Beskrivning

pp_granulo

Datatyp

integer

HP
Beskrivning

pp_subgranu_HP

Datatyp

integer

Beskrivning

pp_subgranu_null

Datatyp

integer

Granulomateous disease other than idiopathic sarcoidosis
Beskrivning

pp_subgranu_Granulomateous disease other than idiopathic sarcoidosis

Datatyp

integer

HP criteria - nonfibrotic Choose from drop down: definite, probable, indeterminate (based on ATS HP guideline) Cellular interstitial pneumonia (bronchiolocentric; cellular NSIP; lymphocyte-predominant)
Beskrivning

pp_granunf_criteria_Cellular interstitial pneumonia (bronchiolocentric; cellular NSIP; lymphocyte-predominant)

Datatyp

integer

Cellular bronchiolitis (lymphocyte predominant; +/- OP with Masson bodies; +/- foamy macrophages)
Beskrivning

pp_granunf_criteria_Cellular bronchiolitis (lymphocyte predominant; +/- OP with Masson bodies; +/- foamy macrophages)

Datatyp

integer

Poorly formed nonnecrotizing granulomas (loose clusters of epithelioid cells +/- intracytoplasmic inclusions; situated in peribronchiolar interstitium
Beskrivning

pp_granunf_criteria_Poorly formed nonnecrotizing granulomas (loose clusters of epithelioid cells +/- intracytoplasmic inclusions; situated in peribronchiolar interstitium

Datatyp

integer

Absence of any of the following: plasma cells > lymphs; extensive lymphoid hyperplasia; extensive well-formed sarcoidal and/or necrotizing granulomas; aspirated particulates
Beskrivning

pp_granunf_criteria_Absence of any of the following: plasma cells > lymphs; extensive lymphoid hyperplasia; extensive well-formed sarcoidal and/or necrotizing granulomas; aspirated particulates

Datatyp

integer

Please choose:
Beskrivning

pp_granunf_category

Datatyp

text

Suggested diagnosis: Definite nonfibrotic (cellular) HP criteria
Beskrivning

pp_nf_granu_definite

Datatyp

text

Suggested diagnosis: Probable nonfibrotic HP criteria
Beskrivning

pp_nf_granu_probable

Datatyp

text

Suggested diagnosis: Indeterminate for non-fibrotic HP criteria
Beskrivning

pp_nf_granu_indeter

Datatyp

text

HP criteria - fibrotic Choose from drop down: definite, probable, indeterminate (based on ATS HP guideline) Chronic fibrosing interstital pneumonia (architectural distortion
Beskrivning

pp_granuf_criteria_Chronic fibrosing interstital pneumonia (architectural distortion

Datatyp

integer

Airway-centered fibrosis (opt. Peribronchiolar metaplasia or Bridging fibrosis)
Beskrivning

pp_granuf_criteria_Airway-centered fibrosis (opt. Peribronchiolar metaplasia or Bridging fibrosis)

Datatyp

integer

Poorly formed non-necrotizing granulomas (opt. Cellular intestinal pneumonia or Cellular bronchiolitis or Organizing pneumonia AND Absence of features in any biopsy site such as plasma cells > lymphs
Beskrivning

pp_granuf_criteria_Poorly formed non-necrotizing granulomas (opt. Cellular intestinal pneumonia or Cellular bronchiolitis or Organizing pneumonia AND Absence of features in any biopsy site such as plasma cells > lymphs

Datatyp

integer

Definite fibrotic HP criteria
Beskrivning

pp_f_granu_definite

Datatyp

text

Probable nonfibrotic HP criteria
Beskrivning

pp_f_granu_probable

Datatyp

text

Indeterminate for fibrotic HP criteria
Beskrivning

pp_f_granu_indeterm

Datatyp

text

Please choose:
Beskrivning

pp_granu_f_category

Datatyp

text

Sarcoidosis criteria as in ATS 2020 Sarcoidosis Guideline (choose appropriate) Presence of granuloma or nodular hyalinised fibrosis representing healed granulomas (scattered multinucleated giant cells may be detectable)
Beskrivning

pp_sarcoidosis_Presence of granuloma or nodular hyalinised fibrosis representing healed granulomas (scattered multinucleated giant cells may be detectable)

Datatyp

integer

Granuloma are compact
Beskrivning

pp_sarcoidosis_Granuloma are compact

Datatyp

integer

Fibrosis beginning at the granuloma periphery with extension centrally into the granuloma
Beskrivning

pp_sarcoidosis_Fibrosis beginning at the granuloma periphery with extension centrally into the granuloma

Datatyp

integer

Lesions are perilymphatic
Beskrivning

pp_sarcoidosis_Lesions are perilymphatic

Datatyp

integer

Sparse surrounding lymphocytic infiltrate
Beskrivning

pp_sarcoidosis_Sparse surrounding lymphocytic infiltrate

Datatyp

integer

Microorganism stains and cultures negative
Beskrivning

pp_sarcoidosis_Microorganism stains and cultures negative

Datatyp

integer

Granulomatous disease other than idiopathic sarcoidosis
Beskrivning

pp_granu_subgranu

Datatyp

text

Infectious
Beskrivning

pp_granu_infectious

Datatyp

text

Non-infectious
Beskrivning

pp_granu_noninfect

Datatyp

text

Idiopathic
Beskrivning

pp_granu_idiopathic

Datatyp

text

Lymphangioleiomyomatosis
Beskrivning

pp_lymphangio

Datatyp

integer

Thin walled cystic air spaces and patchy
Beskrivning

pp_sub_lymphangio_Thin walled cystic air spaces and patchy

Datatyp

integer

Spindle cells are located centrally with peripheral epithelioid cells
Beskrivning

pp_sub_lymphangio_Spindle cells are located centrally with peripheral epithelioid cells

Datatyp

integer

Cyst walls are lined by alveolar and bronchiolar epithelium
Beskrivning

pp_sub_lymphangio_Cyst walls are lined by alveolar and bronchiolar epithelium

Datatyp

integer

Resembles renal angiomyolipoma in that smooth muscle appears to spin off muscle coats of these structures
Beskrivning

pp_sub_lymphangio_Resembles renal angiomyolipoma in that smooth muscle appears to spin off muscle coats of these structures

Datatyp

integer

Muscle cells have optically clear cytoplasm
Beskrivning

pp_sub_lymphangio_Muscle cells have optically clear cytoplasm

Datatyp

integer

Hemosiderin pigment
Beskrivning

pp_sub_lymphangio_Hemosiderin pigment

Datatyp

integer

Pulmonary Alveolar Proteinosis
Beskrivning

pp_pap

Datatyp

integer

Alveoli contain amorphous
Beskrivning

pp_sub_pap_Alveoli contain amorphous

Datatyp

integer

Variable fibrosis
Beskrivning

pp_sub_pap_Variable fibrosis

Datatyp

integer

Mild / no lymphocytic infiltration
Beskrivning

pp_sub_pap_Mild / no lymphocytic infiltration

Datatyp

integer

Amyloidosis
Beskrivning

pp_amyloidosis

Datatyp

integer

Pale pink
Beskrivning

pp_sub_amyloidosis_Pale pink

Datatyp

integer

Characteristic cracking artefact
Beskrivning

pp_sub_amyloidosis_Characteristic cracking artefact

Datatyp

integer

Macrophages and foreign body giant cells may be found around deposits
Beskrivning

pp_sub_amyloidosis_Macrophages and foreign body giant cells may be found around deposits

Datatyp

integer

Labelling with Congo and immunohistochemistry
Beskrivning

pp_sub_amyloidosis_Labelling with Congo and immunohistochemistry

Datatyp

integer

Eosinophilic disease
Beskrivning

pp_eosdisease

Datatyp

integer

Beskrivning

pp_sub_eosdis

Datatyp

text

ILD with lipid storage diseases (Niemann-Pick-disease, Gaucher disease)
Beskrivning

pp_gaucher

Datatyp

integer

Neurofibromatosis
Beskrivning

pp_neurofib

Datatyp

integer

Alveolar microlithiasis
Beskrivning

pp_alveolarmic

Datatyp

integer

Diffuse filling of alveolar air spaces by calcospherites
Beskrivning

pp_sub_alveolarmi_Diffuse filling of alveolar air spaces by calcospherites

Datatyp

integer

Lamellated calcifications
Beskrivning

pp_sub_alveolarmi_Lamellated calcifications

Datatyp

integer

Late stages may show increased localization to subpleural
Beskrivning

pp_sub_alveolarmi_Late stages may show increased localization to subpleural

Datatyp

integer

Fibrosis and ossification may occur in same areas
Beskrivning

pp_sub_alveolarmi_Fibrosis and ossification may occur in same areas

Datatyp

integer

Other vasculitides Please specify in comorbidities
Beskrivning

pp_othervasc

Datatyp

integer

Similar models

Pathological pattern

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
pp_date
Item
Date of assessment
date
Item
Any proof of malignancy?     Please specify in comorbidities
integer
Code List
Any proof of malignancy?     Please specify in comorbidities
CL Item
Yes (1)
CL Item
No (0)
Item
Underlying material for histopathological evaluation
text
Code List
Underlying material for histopathological evaluation
CL Item
EBUS-TBNA (ebus)
CL Item
TBB (tbb)
CL Item
Cryobiopsy (cryo)
CL Item
Transthoracic needle biopsy (transthoraxneedle)
CL Item
Open Lung Biopsy by VATS (vats)
CL Item
Open Lung Biopsy by conventional thoracotomy (thoracotomy)
CL Item
Explanted lung (expllung)
CL Item
Resection (resect)
CL Item
Autopsy (autopsy)
Item
Lymph node station right: 1. Supraclavicular
integer
Code List
Lymph node station right: 1. Supraclavicular
CL Item
Yes (1)
CL Item
No (0)
Item
2. Upper tracheal
integer
Code List
2. Upper tracheal
CL Item
Yes (1)
CL Item
No (0)
Item
3. Prevascular
integer
Code List
3. Prevascular
CL Item
Yes (1)
CL Item
No (0)
Item
4. Lower paratracheal
integer
Code List
4. Lower paratracheal
CL Item
Yes (1)
CL Item
No (0)
Item
5. Subaortic
integer
Code List
5. Subaortic
CL Item
Yes (1)
CL Item
No (0)
Item
6. AP window
integer
Code List
6. AP window
CL Item
Yes (1)
CL Item
No (0)
Item
7. Subcarinal
integer
Code List
7. Subcarinal
CL Item
Yes (1)
CL Item
No (0)
Item
8. Paraesophagheal
integer
Code List
8. Paraesophagheal
CL Item
Yes (1)
CL Item
No (0)
Item
9. Pulmonary ligament
integer
Code List
9. Pulmonary ligament
CL Item
Yes (1)
CL Item
No (0)
Item
10. Hilar
integer
Code List
10. Hilar
CL Item
Yes (1)
CL Item
No (0)
Item
11. Interlobar
integer
Code List
11. Interlobar
CL Item
Yes (1)
CL Item
No (0)
Item
12. Lobar
integer
Code List
12. Lobar
CL Item
Yes (1)
CL Item
No (0)
Item
Lymph node station left: 1. Supraclavicular
integer
Code List
Lymph node station left: 1. Supraclavicular
CL Item
Yes (1)
CL Item
No (0)
Item
2. Upper tracheal
integer
Code List
2. Upper tracheal
CL Item
Yes (1)
CL Item
No (0)
Item
3. Prevascular
integer
Code List
3. Prevascular
CL Item
Yes (1)
CL Item
No (0)
Item
4. Lower paratracheal
integer
Code List
4. Lower paratracheal
CL Item
Yes (1)
CL Item
No (0)
Item
5. Subaortic
integer
Code List
5. Subaortic
CL Item
Yes (1)
CL Item
No (0)
Item
6. AP window
integer
Code List
6. AP window
CL Item
Yes (1)
CL Item
No (0)
Item
7. Subcarinal
integer
Code List
7. Subcarinal
CL Item
Yes (1)
CL Item
No (0)
Item
8. Paraesophagheal
integer
Code List
8. Paraesophagheal
CL Item
Yes (1)
CL Item
No (0)
Item
9. Pulmonary ligament
integer
Code List
9. Pulmonary ligament
CL Item
Yes (1)
CL Item
No (0)
Item
10. Hilar
integer
Code List
10. Hilar
CL Item
Yes (1)
CL Item
No (0)
Item
11. Interlobar
integer
Code List
11. Interlobar
CL Item
Yes (1)
CL Item
No (0)
Item
12. Lobar
integer
Code List
12. Lobar
CL Item
Yes (1)
CL Item
No (0)
Item
Location biopsy upper lobe right: 1. Apical
integer
Code List
Location biopsy upper lobe right: 1. Apical
CL Item
Yes (1)
CL Item
No (0)
Item
2. Posterior
integer
Code List
2. Posterior
CL Item
Yes (1)
CL Item
No (0)
Item
3. Anterior
integer
Code List
3. Anterior
CL Item
Yes (1)
CL Item
No (0)
Item
Location biopsy middle lobe right: 4. Lateral
integer
Code List
Location biopsy middle lobe right: 4. Lateral
CL Item
Yes (1)
CL Item
No (0)
Item
5. Medial
integer
Code List
5. Medial
CL Item
Yes (1)
CL Item
No (0)
Item
Location biopsy lower lobe right: 6. Superior
integer
Code List
Location biopsy lower lobe right: 6. Superior
CL Item
Yes (1)
CL Item
No (0)
Item
7. Med. basal
integer
Code List
7. Med. basal
CL Item
Yes (1)
CL Item
No (0)
Item
8. Lat. basal
integer
Code List
8. Lat. basal
CL Item
Yes (1)
CL Item
No (0)
Item
9. Lat. basal
integer
Code List
9. Lat. basal
CL Item
Yes (1)
CL Item
No (0)
Item
10. Post basal
integer
Code List
10. Post basal
CL Item
Yes (1)
CL Item
No (0)
Item
Location biopsy upper lobe left: 1-2 Apical posterior
integer
Code List
Location biopsy upper lobe left: 1-2 Apical posterior
CL Item
Yes (1)
CL Item
No (0)
Item
3. Anterior
integer
Code List
3. Anterior
CL Item
Yes (1)
CL Item
No (0)
Item
4. Superior (Lingula)
integer
Code List
4. Superior (Lingula)
CL Item
Yes (1)
CL Item
No (0)
Item
5. Inferior (Lingula)
integer
Code List
5. Inferior (Lingula)
CL Item
Yes (1)
CL Item
No (0)
Item
Location biopsy lower lobe left: 6. Superior
integer
Code List
Location biopsy lower lobe left: 6. Superior
CL Item
Yes (1)
CL Item
No (0)
Item
7-8. Ant. basal
integer
Code List
7-8. Ant. basal
CL Item
Yes (1)
CL Item
No (0)
Item
9. Lat. basal
integer
Code List
9. Lat. basal
CL Item
Yes (1)
CL Item
No (0)
Item
10. Post. basal
integer
Code List
10. Post. basal
CL Item
Yes (1)
CL Item
No (0)
Item
IIP patterns (as based on most recent ATS/ERS guidelines)
integer
Code List
IIP patterns (as based on most recent ATS/ERS guidelines)
CL Item
Yes (1)
CL Item
No (0)
Item
IIP patterns UIP
integer
Code List
IIP patterns UIP
CL Item
Yes (1)
CL Item
No (0)
Item
NSIP
integer
CL Item
Yes (1)
CL Item
No (0)
Item
AIP
integer
CL Item
Yes (1)
CL Item
No (0)
Item
OP
integer
CL Item
Yes (1)
CL Item
No (0)
Item
RB-ILD
integer
CL Item
Yes (1)
CL Item
No (0)
Item
DIP
integer
CL Item
Yes (1)
CL Item
No (0)
Item
LIP
integer
CL Item
Yes (1)
CL Item
No (0)
Item
PPFE
integer
CL Item
Yes (1)
CL Item
No (0)
Item
AFOP
integer
CL Item
Yes (1)
CL Item
No (0)
Item
BPIP
integer
CL Item
Yes (1)
CL Item
No (0)
Item
ACIF
integer
CL Item
Yes (1)
CL Item
No (0)
Item
UIP criteria Choose from drop down: definite, probable, indeterminate Dense fibrosis with architectural distortion
integer
Code List
UIP criteria Choose from drop down: definite, probable, indeterminate Dense fibrosis with architectural distortion
CL Item
Yes (1)
CL Item
No (0)
Item
Predominant subpleural and/or paraseptal distribution of fibrosis
integer
Code List
Predominant subpleural and/or paraseptal distribution of fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
Patchy involvement of lung parenchyma by fibrosis
integer
Code List
Patchy involvement of lung parenchyma by fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
Fibroblast foci
integer
Code List
Fibroblast foci
CL Item
Yes (1)
CL Item
No (0)
Item
Honeycombing
integer
Code List
Honeycombing
CL Item
Yes (1)
CL Item
No (0)
Item
Absence of features suggesting an alternate diagnosis
integer
Code List
Absence of features suggesting an alternate diagnosis
CL Item
Yes (1)
CL Item
No (0)
Item
Some histologic features from def. UIP
integer
Code List
Some histologic features from def. UIP
CL Item
Yes (1)
CL Item
No (0)
Item
Fibrosis with or without architectural distortion
integer
Code List
Fibrosis with or without architectural distortion
CL Item
Yes (1)
CL Item
No (0)
Item
Please choose:
text
Code List
Please choose:
CL Item
Definite UIP (definite)
CL Item
Probable UIP (probable)
CL Item
Indeterminate UIP (indeterminate)
pp_uip_definite
Item
Suggested diagnosis: Definite UIP criteria
text
pp_uip_probable
Item
Suggested diagnosis: Probable UIP criteria
text
pp_uip_indeterminate
Item
Suggested diagnosis: Indeterminate UIP criteria
text
Item
NSIP - Cellular
integer
Code List
NSIP - Cellular
CL Item
Yes (1)
CL Item
No (0)
Item
Cellular interstitial pneumonia; lymphocytic or plasmacytic
integer
Code List
Cellular interstitial pneumonia; lymphocytic or plasmacytic
CL Item
Yes (1)
CL Item
No (0)
Item
Diffuse and uniform inflammation ("temporal homogeneity")
integer
Code List
Diffuse and uniform inflammation ("temporal homogeneity")
CL Item
Yes (1)
CL Item
No (0)
Item
Loose interstitial fibrosis
integer
Code List
Loose interstitial fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
Preserved architecture
integer
Code List
Preserved architecture
CL Item
Yes (1)
CL Item
No (0)
Item
NSIP - Fibrotic
integer
Code List
NSIP - Fibrotic
CL Item
Yes (1)
CL Item
No (0)
Item
Depletion of inflammatory cells
integer
Code List
Depletion of inflammatory cells
CL Item
Yes (1)
CL Item
No (0)
Item
Dense fiber-rich interstitial fibrosis
integer
Code List
Dense fiber-rich interstitial fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
Preserved architecture
integer
Code List
Preserved architecture
CL Item
Yes (1)
CL Item
No (0)
pp_aip_discription
Item
AIP - diffuse alveolar damage, almost completely identical to acute respiratory distress syndrome / diffuse alveolar damage morphologically
text
Item
AIP - Exudative phase
integer
Code List
AIP - Exudative phase
CL Item
Yes (1)
CL Item
No (0)
Item
Hyaline membranes in alveolar duct or sacs; scattered or not apparent
integer
Code List
Hyaline membranes in alveolar duct or sacs; scattered or not apparent
CL Item
Yes (1)
CL Item
No (0)
Item
Interstitial and intra-alveolar edema
integer
Code List
Interstitial and intra-alveolar edema
CL Item
Yes (1)
CL Item
No (0)
Item
Collapsed alveoli
integer
Code List
Collapsed alveoli
CL Item
Yes (1)
CL Item
No (0)
Item
Denudation and necrosis of type I pneumocytes
integer
Code List
Denudation and necrosis of type I pneumocytes
CL Item
Yes (1)
CL Item
No (0)
Item
Hemorrhage - usually mild
integer
Code List
Hemorrhage - usually mild
CL Item
Yes (1)
CL Item
No (0)
Item
AIP - Proliferative / organizing phase
integer
Code List
AIP - Proliferative / organizing phase
CL Item
Yes (1)
CL Item
No (0)
Item
Organizing pneumonia with / without remnants of hyaline membrane
integer
Code List
Organizing pneumonia with / without remnants of hyaline membrane
CL Item
Yes (1)
CL Item
No (0)
Item
Interstitial and intra-alveolar proliferation of fibroblasts / myofibroblasts
integer
Code List
Interstitial and intra-alveolar proliferation of fibroblasts / myofibroblasts
CL Item
Yes (1)
CL Item
No (0)
Item
Lymphocytic infiltration; usually more prominent than in acute respiratory distress syndrome
integer
Code List
Lymphocytic infiltration; usually more prominent than in acute respiratory distress syndrome
CL Item
Yes (1)
CL Item
No (0)
Item
Proliferation of type II pneumocytes with occasional cellular atypia
integer
Code List
Proliferation of type II pneumocytes with occasional cellular atypia
CL Item
Yes (1)
CL Item
No (0)
Item
Endothelial injury and fibrinous thromboembolism in arterioles / arteries
integer
Code List
Endothelial injury and fibrinous thromboembolism in arterioles / arteries
CL Item
Yes (1)
CL Item
No (0)
Item
AIP - Fibrosis phase
integer
Code List
AIP - Fibrosis phase
CL Item
Yes (1)
CL Item
No (0)
Item
Diffuse collagenous fibrosis
integer
Code List
Diffuse collagenous fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
Microscopic honeycomb-like change
integer
Code List
Microscopic honeycomb-like change
CL Item
Yes (1)
CL Item
No (0)
Item
Traction bronchiolectasis
integer
Code List
Traction bronchiolectasis
CL Item
Yes (1)
CL Item
No (0)
Item
Squamous metaplasia
integer
Code List
Squamous metaplasia
CL Item
Yes (1)
CL Item
No (0)
Item
Organized thrombus
integer
Code List
Organized thrombus
CL Item
Yes (1)
CL Item
No (0)
Item
Thickening of pleura with dilatation of lymphatic / blood vessels
integer
Code List
Thickening of pleura with dilatation of lymphatic / blood vessels
CL Item
Yes (1)
CL Item
No (0)
Item
OP Fibroblastic plugs in alveolar sacs and ducts (organizing pneumonia) and bronchiolar lumen (bronchiolitis obliterans)
integer
Code List
OP Fibroblastic plugs in alveolar sacs and ducts (organizing pneumonia) and bronchiolar lumen (bronchiolitis obliterans)
CL Item
Yes (1)
CL Item
No (0)
Item
Formed by spindled fibroblasts in pale staining matrix of immature loose collagen with polypoid shape (Masson body) or serpiginous or elongated form
integer
Code List
Formed by spindled fibroblasts in pale staining matrix of immature loose collagen with polypoid shape (Masson body) or serpiginous or elongated form
CL Item
Yes (1)
CL Item
No (0)
Item
Organizing pneumonia sometimes extends from one alveolus to the next one through interalveolar fenestrae (butterfly pattern)
integer
Code List
Organizing pneumonia sometimes extends from one alveolus to the next one through interalveolar fenestrae (butterfly pattern)
CL Item
Yes (1)
CL Item
No (0)
Item
Thickened alveolar septa with lymphocytes
integer
Code List
Thickened alveolar septa with lymphocytes
CL Item
Yes (1)
CL Item
No (0)
Item
Alveolar architecture is usually preserved in cryptogenic organizing pneumonia
integer
Code List
Alveolar architecture is usually preserved in cryptogenic organizing pneumonia
CL Item
Yes (1)
CL Item
No (0)
Item
Foamy macrophage accumulation in surrounding airspace may be present
integer
Code List
Foamy macrophage accumulation in surrounding airspace may be present
CL Item
Yes (1)
CL Item
No (0)
Item
RB-ILD Lightly pigmented (smoker's) macrophages limited to distal airspaces and peribronchiolar airspaces
integer
Code List
RB-ILD Lightly pigmented (smoker's) macrophages limited to distal airspaces and peribronchiolar airspaces
CL Item
Yes (1)
CL Item
No (0)
Item
Pigment within macrophage cytoplasm is yellow to light brown and finely granular
integer
Code List
Pigment within macrophage cytoplasm is yellow to light brown and finely granular
CL Item
Yes (1)
CL Item
No (0)
Item
Minimal to absent peribronchiolar interstitial thickening by fibrosis
integer
Code List
Minimal to absent peribronchiolar interstitial thickening by fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
No diffuse interstitial fibrosis or inflammation
integer
Code List
No diffuse interstitial fibrosis or inflammation
CL Item
Yes (1)
CL Item
No (0)
Item
DIP Diffuse and massive accumulation of intra-alveolar macrophages (smoker's macrophages)
integer
Code List
DIP Diffuse and massive accumulation of intra-alveolar macrophages (smoker's macrophages)
CL Item
Yes (1)
CL Item
No (0)
Item
Brown pigments
integer
Code List
Brown pigments
CL Item
Yes (1)
CL Item
No (0)
Item
Giant cells can be also seen
integer
Code List
Giant cells can be also seen
CL Item
Yes (1)
CL Item
No (0)
Item
Diffuse and homogeneous involvement (similar to NSIP) along with alveolar macrophages
integer
Code List
Diffuse and homogeneous involvement (similar to NSIP) along with alveolar macrophages
CL Item
Yes (1)
CL Item
No (0)
Item
Lymphoid follicles and eosinophils are often present
integer
Code List
Lymphoid follicles and eosinophils are often present
CL Item
Yes (1)
CL Item
No (0)
Item
LIP Lymphoid follicles with germinal centers
integer
Code List
LIP Lymphoid follicles with germinal centers
CL Item
Yes (1)
CL Item
No (0)
Item
Bronchovascular bundles and interlobular septa are usually involved
integer
Code List
Bronchovascular bundles and interlobular septa are usually involved
CL Item
Yes (1)
CL Item
No (0)
Item
Alveolar structure is often inflated and disrupted
integer
Code List
Alveolar structure is often inflated and disrupted
CL Item
Yes (1)
CL Item
No (0)
Item
Typically CD8+ or CD4+ T cells or B cells predominate
integer
Code List
Typically CD8+ or CD4+ T cells or B cells predominate
CL Item
Yes (1)
CL Item
No (0)
Item
Interstitial or intra-alveolar giant cells
integer
Code List
Interstitial or intra-alveolar giant cells
CL Item
Yes (1)
CL Item
No (0)
Item
Intra-alveolar macrophages
integer
Code List
Intra-alveolar macrophages
CL Item
Yes (1)
CL Item
No (0)
Item
Type II pneumocyte hyperplasia
integer
Code List
Type II pneumocyte hyperplasia
CL Item
Yes (1)
CL Item
No (0)
Item
Cyst formation without marked fibrosis
integer
Code List
Cyst formation without marked fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
PPFE Linear subpleural elastofibrosis
integer
Code List
PPFE Linear subpleural elastofibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
Onset in upper lung
integer
Code List
Onset in upper lung
CL Item
Yes (1)
CL Item
No (0)
Item
May be associated to UIP pattern in lower lung parts
integer
Code List
May be associated to UIP pattern in lower lung parts
CL Item
Yes (1)
CL Item
No (0)
Item
AFOP Dominant findings of intra-alveolar fibrin
integer
Code List
AFOP Dominant findings of intra-alveolar fibrin
CL Item
Yes (1)
CL Item
No (0)
Item
Involves more than 20% of the alveolar spaces in the lesion
integer
Code List
Involves more than 20% of the alveolar spaces in the lesion
CL Item
Yes (1)
CL Item
No (0)
Item
Neutrophils are usually scanty or absent
integer
Code List
Neutrophils are usually scanty or absent
CL Item
Yes (1)
CL Item
No (0)
Item
Organizing pneumonia: fibroblastic plugs in alveolar sacs and ducts with loose collagen matrix
integer
Code List
Organizing pneumonia: fibroblastic plugs in alveolar sacs and ducts with loose collagen matrix
CL Item
Yes (1)
CL Item
No (0)
Item
Diffuse and patchy distribution
integer
Code List
Diffuse and patchy distribution
CL Item
Yes (1)
CL Item
No (0)
Item
BPIP Peribronchiolar metaplasia
integer
Code List
BPIP Peribronchiolar metaplasia
CL Item
Yes (1)
CL Item
No (0)
Item
Peribronchiolar fibrosis with preserved architecture
integer
Code List
Peribronchiolar fibrosis with preserved architecture
CL Item
Yes (1)
CL Item
No (0)
Item
Under discussion
integer
Code List
Under discussion
CL Item
Yes (1)
CL Item
No (0)
Item
ACIF
integer
Code List
ACIF
CL Item
Yes (1)
CL Item
No (0)
Item
Langerhans Cell Histiocytosis (LCH)
integer
Code List
Langerhans Cell Histiocytosis (LCH)
CL Item
Yes (1)
CL Item
No (0)
Item
Accumulation of activated LCs organised into loose
integer
Code List
Accumulation of activated LCs organised into loose
CL Item
Yes (1)
CL Item
No (0)
Item
Infiltration with Lymphocytes and other inflammatory cells
integer
Code List
Infiltration with Lymphocytes and other inflammatory cells
CL Item
Yes (1)
CL Item
No (0)
Item
Abundance of pigmented macrophages
integer
Code List
Abundance of pigmented macrophages
CL Item
Yes (1)
CL Item
No (0)
Item
Granulomateous patterns
integer
Code List
Granulomateous patterns
CL Item
Yes (1)
CL Item
No (0)
Item
HP
integer
Code List
HP
CL Item
Yes (1)
CL Item
No (0)
Item
integer
CL Item
Yes (1)
CL Item
No (0)
Item
Granulomateous disease other than idiopathic sarcoidosis
integer
Code List
Granulomateous disease other than idiopathic sarcoidosis
CL Item
Yes (1)
CL Item
No (0)
Item
HP criteria - nonfibrotic Choose from drop down: definite, probable, indeterminate (based on ATS HP guideline) Cellular interstitial pneumonia (bronchiolocentric; cellular NSIP; lymphocyte-predominant)
integer
Code List
HP criteria - nonfibrotic Choose from drop down: definite, probable, indeterminate (based on ATS HP guideline) Cellular interstitial pneumonia (bronchiolocentric; cellular NSIP; lymphocyte-predominant)
CL Item
Yes (1)
CL Item
No (0)
Item
Cellular bronchiolitis (lymphocyte predominant; +/- OP with Masson bodies; +/- foamy macrophages)
integer
Code List
Cellular bronchiolitis (lymphocyte predominant; +/- OP with Masson bodies; +/- foamy macrophages)
CL Item
Yes (1)
CL Item
No (0)
Item
Poorly formed nonnecrotizing granulomas (loose clusters of epithelioid cells +/- intracytoplasmic inclusions; situated in peribronchiolar interstitium
integer
Code List
Poorly formed nonnecrotizing granulomas (loose clusters of epithelioid cells +/- intracytoplasmic inclusions; situated in peribronchiolar interstitium
CL Item
Yes (1)
CL Item
No (0)
Item
Absence of any of the following: plasma cells > lymphs; extensive lymphoid hyperplasia; extensive well-formed sarcoidal and/or necrotizing granulomas; aspirated particulates
integer
Code List
Absence of any of the following: plasma cells > lymphs; extensive lymphoid hyperplasia; extensive well-formed sarcoidal and/or necrotizing granulomas; aspirated particulates
CL Item
Yes (1)
CL Item
No (0)
Item
Please choose:
text
Code List
Please choose:
CL Item
Definite HP criteria (definite)
CL Item
Probable HP criteria (probable)
CL Item
Indeterminate HP criteria (indeterminate)
pp_nf_granu_definite
Item
Suggested diagnosis: Definite nonfibrotic (cellular) HP criteria
text
pp_nf_granu_probable
Item
Suggested diagnosis: Probable nonfibrotic HP criteria
text
pp_nf_granu_indeter
Item
Suggested diagnosis: Indeterminate for non-fibrotic HP criteria
text
Item
HP criteria - fibrotic Choose from drop down: definite, probable, indeterminate (based on ATS HP guideline) Chronic fibrosing interstital pneumonia (architectural distortion
integer
Code List
HP criteria - fibrotic Choose from drop down: definite, probable, indeterminate (based on ATS HP guideline) Chronic fibrosing interstital pneumonia (architectural distortion
CL Item
Yes (1)
CL Item
No (0)
Item
Airway-centered fibrosis (opt. Peribronchiolar metaplasia or Bridging fibrosis)
integer
Code List
Airway-centered fibrosis (opt. Peribronchiolar metaplasia or Bridging fibrosis)
CL Item
Yes (1)
CL Item
No (0)
Item
Poorly formed non-necrotizing granulomas (opt. Cellular intestinal pneumonia or Cellular bronchiolitis or Organizing pneumonia AND Absence of features in any biopsy site such as plasma cells > lymphs
integer
Code List
Poorly formed non-necrotizing granulomas (opt. Cellular intestinal pneumonia or Cellular bronchiolitis or Organizing pneumonia AND Absence of features in any biopsy site such as plasma cells > lymphs
CL Item
Yes (1)
CL Item
No (0)
pp_f_granu_definite
Item
Definite fibrotic HP criteria
text
pp_f_granu_probable
Item
Probable nonfibrotic HP criteria
text
pp_f_granu_indeterm
Item
Indeterminate for fibrotic HP criteria
text
Item
Please choose:
text
Code List
Please choose:
CL Item
Definite (definite)
CL Item
Probable (probable)
CL Item
Indeterminate (indeterminate)
Item
Sarcoidosis criteria as in ATS 2020 Sarcoidosis Guideline (choose appropriate) Presence of granuloma or nodular hyalinised fibrosis representing healed granulomas (scattered multinucleated giant cells may be detectable)
integer
Code List
Sarcoidosis criteria as in ATS 2020 Sarcoidosis Guideline (choose appropriate) Presence of granuloma or nodular hyalinised fibrosis representing healed granulomas (scattered multinucleated giant cells may be detectable)
CL Item
Yes (1)
CL Item
No (0)
Item
Granuloma are compact
integer
Code List
Granuloma are compact
CL Item
Yes (1)
CL Item
No (0)
Item
Fibrosis beginning at the granuloma periphery with extension centrally into the granuloma
integer
Code List
Fibrosis beginning at the granuloma periphery with extension centrally into the granuloma
CL Item
Yes (1)
CL Item
No (0)
Item
Lesions are perilymphatic
integer
Code List
Lesions are perilymphatic
CL Item
Yes (1)
CL Item
No (0)
Item
Sparse surrounding lymphocytic infiltrate
integer
Code List
Sparse surrounding lymphocytic infiltrate
CL Item
Yes (1)
CL Item
No (0)
Item
Microorganism stains and cultures negative
integer
Code List
Microorganism stains and cultures negative
CL Item
Yes (1)
CL Item
No (0)
Item
Granulomatous disease other than idiopathic sarcoidosis
text
Code List
Granulomatous disease other than idiopathic sarcoidosis
CL Item
Infectious (infectious)
CL Item
Non-infectious (non-infectious)
CL Item
Idiopathic (idiopathic)
Item
Infectious
text
Code List
Infectious
CL Item
Bacteria (e.g. M. tuberculosis, MOTT, Brucella, Tropheryma whipplei, M. leprae, Francisella tularensis, Bartonella henselae, Coxiella burnetii) (bacteria)
CL Item
Fungi (Aspergillus, Histoplasma, Blastomyces, Coccidioides, Cryptococcus, Pneumocystis) (fungi)
CL Item
Viruses (Herpes Zoster) (virus)
CL Item
Parasites (Toxoplasma gondii, Schistosomes, Leishmania, Enterobius, Dirofilaria) (parasite)
Item
Non-infectious
text
Code List
Non-infectious
CL Item
Malignancy (Lymphoma, lymphomatoid granulomatosis, sarcoid-like reaction to tumor, germ cell tumor) (malignancy)
CL Item
Autoimmune (ANCA-associated vasculitides, GLILD associated with CVID, rheumatoid nodules, Langerhans Cell histiocytosis, IgG4-related disease, inflammatory bowel diseases, primary biliary cholangitis, primary sclerosing cholangitis, autoimmune hepatitis) (autoimmune)
CL Item
Exposures (HP, "Hot tub lung syndrome", Pneumoconiosis (e.g. berylliosis), drug-induced ILD (e.g. treatment with checkpoint inhibitors), anti-TNF or biologicals, foreign body granulomatosis (e.g. talc, tattoo), steatosis (lipogranulomas)) (exposures)
Item
Idiopathic
text
Code List
Idiopathic
CL Item
Necrotizing sarcoid granulomatosis (necrotizing)
CL Item
Histiocytic necrotizing lymphadenitis (Kikuchi´s disease) (histiocytic)
CL Item
Granulomatous Lesion of Unknown Significance (glus)
CL Item
Bronchocentric granulomatosis (bronchogranu)
Item
Lymphangioleiomyomatosis
integer
Code List
Lymphangioleiomyomatosis
CL Item
Yes (1)
CL Item
No (0)
Item
Thin walled cystic air spaces and patchy
integer
Code List
Thin walled cystic air spaces and patchy
CL Item
Yes (1)
CL Item
No (0)
Item
Spindle cells are located centrally with peripheral epithelioid cells
integer
Code List
Spindle cells are located centrally with peripheral epithelioid cells
CL Item
Yes (1)
CL Item
No (0)
Item
Cyst walls are lined by alveolar and bronchiolar epithelium
integer
Code List
Cyst walls are lined by alveolar and bronchiolar epithelium
CL Item
Yes (1)
CL Item
No (0)
Item
Resembles renal angiomyolipoma in that smooth muscle appears to spin off muscle coats of these structures
integer
Code List
Resembles renal angiomyolipoma in that smooth muscle appears to spin off muscle coats of these structures
CL Item
Yes (1)
CL Item
No (0)
Item
Muscle cells have optically clear cytoplasm
integer
Code List
Muscle cells have optically clear cytoplasm
CL Item
Yes (1)
CL Item
No (0)
Item
Hemosiderin pigment
integer
Code List
Hemosiderin pigment
CL Item
Yes (1)
CL Item
No (0)
Item
Pulmonary Alveolar Proteinosis
integer
Code List
Pulmonary Alveolar Proteinosis
CL Item
Yes (1)
CL Item
No (0)
Item
Alveoli contain amorphous
integer
Code List
Alveoli contain amorphous
CL Item
Yes (1)
CL Item
No (0)
Item
Variable fibrosis
integer
Code List
Variable fibrosis
CL Item
Yes (1)
CL Item
No (0)
Item
Mild / no lymphocytic infiltration
integer
Code List
Mild / no lymphocytic infiltration
CL Item
Yes (1)
CL Item
No (0)
Item
Amyloidosis
integer
Code List
Amyloidosis
CL Item
Yes (1)
CL Item
No (0)
Item
Pale pink
integer
Code List
Pale pink
CL Item
Yes (1)
CL Item
No (0)
Item
Characteristic cracking artefact
integer
Code List
Characteristic cracking artefact
CL Item
Yes (1)
CL Item
No (0)
Item
Macrophages and foreign body giant cells may be found around deposits
integer
Code List
Macrophages and foreign body giant cells may be found around deposits
CL Item
Yes (1)
CL Item
No (0)
Item
Labelling with Congo and immunohistochemistry
integer
Code List
Labelling with Congo and immunohistochemistry
CL Item
Yes (1)
CL Item
No (0)
Item
Eosinophilic disease
integer
Code List
Eosinophilic disease
CL Item
Yes (1)
CL Item
No (0)
Item
text
Code List
CL Item
Acute eosinophilic pneumonia (known cause such as smoking and other inhalants, drugs or infections) or idiopathic (acuteeos)
CL Item
Chronic eosinophilic pneumonia (known causes such as drugs, infections, CV-ILD or idiopathic) (chroniceos)
CL Item
Loeffler's syndrome (known causes such as infections, especially parasites, drugs or idiopathic) (loefflerssynd)
CL Item
Predominant airway disease (as in asthma or allergic bronchopulmonary aspergillosis) (predominantair)
Item
ILD with lipid storage diseases (Niemann-Pick-disease, Gaucher disease)
integer
Code List
ILD with lipid storage diseases (Niemann-Pick-disease, Gaucher disease)
CL Item
Yes (1)
CL Item
No (0)
Item
Neurofibromatosis
integer
Code List
Neurofibromatosis
CL Item
Yes (1)
CL Item
No (0)
Item
Alveolar microlithiasis
integer
Code List
Alveolar microlithiasis
CL Item
Yes (1)
CL Item
No (0)
Item
Diffuse filling of alveolar air spaces by calcospherites
integer
Code List
Diffuse filling of alveolar air spaces by calcospherites
CL Item
Yes (1)
CL Item
No (0)
Item
Lamellated calcifications
integer
Code List
Lamellated calcifications
CL Item
Yes (1)
CL Item
No (0)
Item
Late stages may show increased localization to subpleural
integer
Code List
Late stages may show increased localization to subpleural
CL Item
Yes (1)
CL Item
No (0)
Item
Fibrosis and ossification may occur in same areas
integer
Code List
Fibrosis and ossification may occur in same areas
CL Item
Yes (1)
CL Item
No (0)
Item
Other vasculitides Please specify in comorbidities
integer
Code List
Other vasculitides Please specify in comorbidities
CL Item
Yes (1)
CL Item
No (0)