Lung Review Flashcards

1
Q

Diffuse alveolar damage patterns?

What is Acute Fibrinous and Organizing Pneumonia?

A

Acute: >1 wk; Hyaline membranes and type 2 cell hyperplasia with fibrin thrombi

Organizing: >1 wk. Fibrosis in septa and remains of membranes

DAD variant without Hyaline membranes: Fibrin and organization present

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2
Q

Organizing pneumonia/BOOP has what on H and E?

A

Masson Bodies/Fibroblastic plugs and associated alveolar thickening

See in many things including other diseases and even abscesses and cancers

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3
Q

Obliterative Bronchiolitis H and E?

Seen in?

A

AKA: Constrictive bronchiolitis obliterans
Submucosal scaring in bronchioles

Associated with: Lung transplants, GVHD, Adenovirus

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4
Q

Actinomyces staining pattern?

Associated with?

Nocardia pattern?
Associated with?

A

Long branching rods, Gram +, Silver +, AFB -

Poor dentition

Nocardia: Long branching rods, Gram +, SIlver +, Weakly AFB +

Immunocompromised

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5
Q

Hot tub lung and ddx?

Which fungi are vascular invasive and infarction?

A

From MAC; Well Formed Non-nec granulomas; hypersensitivity pneumonitis (poorly formed)

Aspergillous and Mucor; Candia causes inflammation

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6
Q

What is seen in allergic bronchopulmonary aspergillosis?

AIDS patient with intra-alveolar froth or patient with DAD rule out?

A

Hypersensitivity reaction, Path: Mucoid impaction (layered) in bronchi, eosinophils, broncogenic granulomas

PJP pneumonia!

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7
Q

HIsto H and E?

Location?

Coccidio H and E?
Location?

A

Small yeasts 2-5 um; Ohio Valley

Larger spheres 20-60 um w/ endospores

SW US

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8
Q

Cryptococcus H and E?

Locaiton?

Blasto H and E?

Locaiton?

Dirofilaria H and E?

A

Wide capsular halo (Mucecarmine +); narrow budding
Assoc w/ Pigeons

Yeasts 25 um, Broad based budding; Mucicarmine -

Central and SE USA

Complex with Cuticle

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9
Q

Silica quartz vs amorphous which is worse?

Nodular silicosis H and E?

Acute silicosis casues?

A

Quartz!

Well circumscribed noduled with rim of histeocytes and eventual progressive massive fibrosis

Alveolar proteinosis

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10
Q

MIxed dust fibrosis differs from silicosis by?

Some things asbestos can cause?

A

Mixed dust: Stellate “medusa head fibrosis” vs well circumscribed nodules

Asbestosis, rounded atelectasis, carcinoma
Pluera: Plaques, effusions, mesothelioma

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11
Q

Asbestosis dx requirements?

Berrilliosis H and E?

A

Pulmonary fibrosis and 2 or more asbestos bodies in 1 cm2 of a 5 um thick lung; high counts of fibers in lung digest

Fe Stain Helps

See Sarcoid like granulomas: Need history

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12
Q

Hard metal pnemonocosis (2 metals) and H and E finding?

A

Tungsten and Cobalt; Giant cell interstital pneumonia

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13
Q

UIP Pattern?

Associated with?

A

Varigated apperance: “old and young fibrosis”, Honeycomb fibrosis, Fibroplastic plugging and normal lung

IFP, Connective tissues disease and chronic hypersensitivity pneumona

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14
Q

Nonspecific interstital pneumonia H and E?

Associated with?

A

Uniform pattern: Mild-moderate chronic inflammation, interstital fibrosis +/- inflammation

Idiopathic NSIP, Connective tissue disease, hypersensitivity, drug tox, infection

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15
Q

Respiratory bronchiolitis H and E?

Which population is this normal in?

Desquamative Interstital Pneumonia H and E?

A

Bronchiolocentric intra-alveolar macrophages

SMOKERS

Like worse RB; Uniform with diffuse intraalveolar macrophages and possible fibrosis

Also seen in smokers!

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16
Q

Lymphoid interstital pneumona main R/O?

Associated conditions?

A

LYMPHOMA

Immunodeficiency (HIV kids) and connective tissue disease

17
Q

Pleuroparenchemal fibroroelastosis H and E?

Associated conditions?

Needs imaging to distinguish from?

A

Visceral pleura fibrosis, Subpleural fibroelastosis, Sparing of parenchyma far from pleura with abrupt transitions

Associated wtih: Idiopathic PPFE and Lung allograft rejection

Apical cap

18
Q

Sarcoid H and E?

Hypersensitivity pneumonitis H and E?

A

Well formed granulomas with some possible coalescence

HP: Bronochiolocentric intersitial pneumonia, cellular bronchiolitis, vague fromed granulomas, orangizing pneumonia

19
Q

Lymphangioleiomyomatosis (LAM) population?
Associated with?

H and E?

IHC?

A

Low grade neoplasm of PEComa; F childbearing age

Tuberous sclerosis (TSC1 and 2 even in sporatic cases)

See holes: Beta-Catenin +, HMB-45, Melan A

20
Q

Pulmonary Lagerhans Histiocytosis population?
H and E?
Stains?

PLH vs Chronic eosinophilic pneumonia?

A

Smokers!

Stellate nodules interstital fibrosis nodules around bronchioles with Langerhans cells at periphery; some eosinophils

S-100+, CD1a+, Langerin +

CEP: Macrophages and eosinophils in alveolar spaces

21
Q

Pulmonary vasculitis is treated with what?

c-ANCA is seen in what lung vasculitis?

p-ANCA is seen in what lung vasculitis?

A

Steroids

Granulomatosis with polyangitis; PR3+ in ELISA

Eosinophilic granulomatosis with polyangitis and microscopic polyangitis. MPO+

22
Q

Granulomatous with polyangitis (Wegner’s) other body locations

H and E and ANCA?

A

Upper respiratory tract, lung, kidneys; c-ANCA/PR3+

Large parenchymal necrosis; neudtrophilic microabscesses and mixed inflammation with giant cells, Vasculitis

23
Q

Eosinophilic Granulomatosis with Polyangitis (Churg Strauss) ANCA?

Criteria/H and E?

A

p-ANCA+/MPO

Asthma, >10% eos’s, Mono/poly neuropathy, Pulmonary opascities, paransal sinus abnormaltiies, biopsy shows increased esos

Asthmatic bronchitis, eosinophilic pneumonia, “Allergic granulomas”, Vasculitis

24
Q

Microscopic polyangitis (Hypersensitivity vasculitis, leukocytoclastic vasculitis, Systemic necrotizing vasculitis); ANCA?

H and E?

A

p-ANCA/MPO

Alveolar hemorrhage, hemosiderin laden macrophages, Neutrophilic capilleritis (in speta and not alveolar spaces)

25
Q

Anti-GBM disease (Goodpasture) patient population?

IF Pattern?

Dx criteria?

A

Young male smoker

Linear
Alvolar hemorrage, Glomerulonephritis, Serum Anti-GBM Ab

Linear IF

26
Q

Atypical adenomatous hyperplasia cell type/size?

Adenocarcinoma in situ size cut off/growth pattern?

Minimally invasise size/invasion cut off?

What to think of outside of these criteria?

A

Atypical Type 2 proliferation, <0.5cm

<3.0 cm; lepidic; Non invasive

<3.0 in size and <0.5 cm invasion

If >3 cm or 0.5 cm invasive or multiple nodules or not circumscribed=Invasive mucinous adenocarcinoma

27
Q
A
28
Q

Adenocarcinoma must be tested for?

NGS adds?

What to test if EGFR treatment is resistant?

A

EGFR (treatment), ALK, ROS1

AKL/ROS are FISH or IHC

NGS adds: ERBB2, MET, BRAF, KRAS

EGFR T700M

29
Q

Carcinoid criteria?

Atypical?

Large cell?

Diffuse idiopathic neuroendocrine cell hyperplasia (just know it is a thing)

A

Less than 2 mits/ 10 HPF; No necrosis

Atypical: 2-10 mites/10 HPF with some necrosis

>10 mites/10 HPF, necrosis (large); cyto features of non small carcinoma; NE by IHC

DIPNAC: Generalized proliferation of lung NE cells

30
Q

Patternless pattern, hyper and hypocellular areas, and Ropey Collagen?

Best predictor of prognosis?

A

Think SFT! Stat6+, and CD34+

Most: >4 mites/2mm2
Less reliable: Size, atypia, necrosis