Pulmonary Pathology III Flashcards

1
Q

Most common lung cancers

A

Adenocarcinoma (38%)
Squamous cell carcinoma (20%)
Small cell (neuroendocrine) carcinoma (14%)
Large cell carcinoma (3%)

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2
Q

What is the progression of normal lung tissue to adenocarcinoma?

A
  1. Normal
  2. AAH (atypical adenomatous hyperplasia)
  3. AIS (adenocarcinoma in situ)
  4. Adenocarcinoma
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3
Q

Atypical adenomatous hyperplasia (AAH) size:

Histological appearance:

A

<5 mm

Dysplastic pneumocytes present along alveoli w/ some interstitial fibrosis. Leads to AIS.

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4
Q

Adenocarcinoma in situ (AIS) size:

Histological appearance:

A

<3 cm

Dysplastic pneumocytes confluently growing along along alveoli. Follows AAH.

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5
Q

Pulmonary adenocarcinoma shows which structures as malignant?

What does it arise from?

A

Glands invade the surrounding lung tissue.

Can arise from precursors or develop de novo.

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6
Q

What does Mucinous Adenocarcinoma mimic?

A

Pneumonia

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7
Q

What is the progression of squamous carcinoma?

A
  1. Normal epithelium
  2. Squamous metaplasia
  3. Squamous carcinoma in situ
  4. Invasive squamous carcinoma
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8
Q

What people are more likely to get squamous carcinoma?

A

More common in men, strong correlation w/ smoking.

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9
Q

Where does squamous carcinoma tend to begin?

A

Centrally

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10
Q

What key histological characteristic suggests squamous carcinoma?

A

Keratin pearls and orange cytoplasm

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11
Q

Small cell (neuroendocrine) carcinoma

What is the grade of the malignancy?

A

Almost always associated w/ smoking.
High rate of mets.

Neuroendocrine carcinoma grade 3.

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12
Q

What are the treatment recommendations for Small cell (neuroendocrine) carcinoma?

A

Surgery not recommended if metastatic to LNs.

Specific chemo is available. Good response to chemo and radiation, but there is a high rate of recurrence.

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13
Q

What molecular markers can be used to identify Adenocarcinoma?

A

EGFR
ALK
PDL-1

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14
Q

What paraneoplastic syndrome is associated w/ squamous carcinoma?

A

Hypercalcemia: PTH-related peptide

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15
Q

What paraneoplastic syndromes are associated w/ Small cell carcinoma?

A

SIADH - too much ADH secretion.

Cushing’s syndrome - secretion of ACTH.

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16
Q

Why might Horner’s syndrome develop in a patient with a pulmonary malignancy?

SX of Horner’s syndrome

A

In superior lung cancers where they can affect the cervical sympathetic plexus.

Enophthalmos - sunken eye ball
Ptosis - drooping of eyelid
Miosis - small pupil
Anhidrosis - no sweating on IL side of face

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17
Q

What kind of tumor is Diffuse pulmonary neuroendocrine cell hyperplasia (DIPNECH)?

What detects them?

What is their size?

A

Neuroendocrine tumor.

High-res CT.

<5 mm (“tumorlets”).

18
Q

What kind of tumor is a carcinoid tumor?

What makes these tumors important?

What is their size?

A

Neuroendocrine tumor.

5 mm or bigger.

Capable of metastasizing.

19
Q

How are carcinoid tumors classified?

A

Indolent - neuroendocrine carcinoma grade 1.

20
Q

Atypical carcinoid tumor is classified as:

What is the likelihood of mets?

What are the chances of survival?

A

Neuroendocrine tumor grade 2.

Increased rate of mets.

Lower survival rate (but better than SCC).

21
Q

How does atypical carcinoid tumor and carcinoid tumor differ?

A

Atypical carcinoid tumors have:

Increased mitotic activity
Necrosis
Disorderly growth

22
Q

What are the SX of carcinoid syndrome?

A

Flushing, diarrhea, cyanosis.

23
Q

5-year survival rates for:

Carcinoid tumors (NE carcinoma grade 1)

Atypical carcinoid tumors (NE carcinoma grade 2)

Small cell carcinoma tumors (NE carcinoma grade 3)

A

Carcinoid tumors (NE carcinoma grade 1) - 95%

Atypical carcinoid tumors (NE carcinoma grade 2) - 70%

Small cell carcinoma tumors (NE carcinoma grade 3) - 5%

24
Q

What makes up a pulmonary hamartoma?

What is it called when seen on CT?

A

Fibrous tissue w/ benign glandular epithelium around hyaline cartilage.

“Coin” lesion.

25
Q

Lymphangioleiomyomatosis (LAM) occurs in:

What LoF is it associated with?

What is the pathogenesis?

What type of cells are found in the BX?

What else does it present w/ often?

A

Young women.

TSC2.

Proliferation of cells creating cystic spaces.

Modified SM cells, which are positive for melanoma markers (HMB-45). Perivascular epithelioid cells.

Pneumothorax, due to “popping” of the cystic space.

26
Q

What is the most common cause of transudative (liquid) pleural effusions?

A

Heart failure

27
Q

What are the most common causes of exudative (inflammatory) pleural effusions?

A

Infection

Malignancy

28
Q

What makes up an empyema?

What structures does it almost always create?

What does the fluid look like?

A

An inflammatory exudate w/ accumulation of pus, usually from a bacterial infection.

Loculations - web-like traps for fluid.

Thick, yellow. Will have neutrophils and bacteria.

29
Q

Which patients are at greatest risk for primary (idiopathic) pneumothorax? How?

A

Young pts. via rupture of subpleural blebs.

30
Q

What causes a tension pneumothorax?

A

Injury to chest wall resulting in one-way valve allowing air into the pleural space, but not out.

It is expansion of the chest wall, but not necessarily the lungs, that is responsible for respiration.

In a closed system, air is a space-occupying lesion.

31
Q

What can cause a secondary pneumothorax?

A
Cystic infections
Cystic tumors
Rupture of blebs
Trauma
Positive-pressure ventilation
32
Q

What is the pressure differences in the pleural cavity compared to atmospheric in primary vs. tension pneumothorax?

A

Primary - pleural cavity pressure < atm.

Tension - pleural cavity pressure > atm.

33
Q

Solitary fibrous tumor are what kind of tumors? Where are they located?

What is its shape?

A

Benign (when small and pedunculated) tumors of the pleura. Larger ones may behave like sarcomas.

CIrcumscribed.

34
Q

What are 3 variants of Mesothelioma?

What is a stain that can help distinguish it from Adenocarcinoma?

A

Epithelioid, Sarcomatoid, Mixed.

Calretinin.

35
Q

How is Mesothelioma treated?

Is it responsive to chemo/radiation?

What is the prognosis?

A

Difficult to treat, as it cannot be excised surgically.

Limited responsiveness to chemo/radiation.

Most pts. will not live after 2 yrs.

36
Q

Which malignancies develop proximally, in various locations, and peripherally?

A

Proximal - squamous cell carcinoma
Various - small-cell NE carcinoma
Peripherally - adenocarcinoma

37
Q

Which cancer exhibits some degree of the 2-hit theory?

What other lung cancer can it exist with?

A

Small-cell NE carcinoma: Rb goes first, then p53.

Can exist w/ squamous cell carcinoma.

38
Q

What should be considered if a pt. has pneumonia-like SX, but does not respond to any therapy?

A

Mucinous adenocarcinoma

39
Q

How is mucinous adenocarcinoma differentiated from AIS?

A

Size. Mucinous adenocarcinoma > 3 cm.

40
Q

What is the course of action once a DX of small-cell NE carcinoma is made?

A

PET CT due to high likelihood of mets.

41
Q

If the effusion is bloody, what would be a concern?

If effusion is pale-yellow, what is a likely DX?

If effusion is white and chalky, what is a concern?

A

Metastases

HF, a transudative effusion

A neoplasm that blocks thoracic duct. Or post-op where the thoracic duct is clipped.