Spleen and Thymus Pathology Flashcards

1
Q

What are 2 congenital splenic anomalies?

A

Congenital absence - rare

Accessory spleens - common

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2
Q

What is a worrisome complication of splenic insufficiency? Why?

A

Sepsis from encapsulated bacteria due to the loss of filtering and antibody production.

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3
Q

What symptoms may be noticed with splenomegaly?

A

LUQ mass effect leading to gastric/abdominal involvement.

Anemia, leukopenia or thrombocytopenia

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4
Q

Splenic rupture is common in which entities?

A

Mono
Malaria
Typhoid fever
Lymphoid neoplasms

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5
Q

What is hypersplenism?

When does it most commonly arise?

Is there a correlation between size of the spleen and severity of cytopenia?

A

A condition where the spleen becomes increasingly active and tends to remove circulating cells/cell products.

It is often in the setting of splenomegaly and commonly secondary to portal HTN and hematological disorders.

No, there is no correlation.

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6
Q

What is the cause of non-specific acute splenitis?

What happens to the spleen grossly and morphologically?

A

Secondary, non-specific reaction to any blood-borne infection.

Mild splenomegaly that is soft and fluctuant.
There is acute congestion of red pulp with infiltrates of neutrophils, plasma cells and +/- eosinophils.

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7
Q

What are 3 causes of congestive splenomegaly?

A
  1. Systemic, central or venous congestion.
    - cardiac decompensation.
  2. Cirrhosis of the liver (most common etiology).
  3. Obstruction of the extrahepatic portal or splenic veins.
    - portal thrombosis, compression, etc. leading to mild-moderate enlargement. May have a sudden onset.
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8
Q

What is Budd-Chiari syndrome?

A

Occlusion of the hepatic v. It presents with abdominal pain, ascites and hepatomegaly. There is also a risk of splenomegaly. Mortality is high if not treated.

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9
Q

What morphological changes occur with congestive splenomegaly?

A

The spleen becomes more fibrous and cellular (often with hypersplenism) along with mineral/pigment deposition.

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10
Q

What causes a splenic infarct?

What is the downstream effect?

A

Occlusion of splenic aa. (cardiac emboli, sickle cell disease).

It can lead to decreased splenic function leading to an increased risk for infection.

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11
Q

What type of neoplasia occurs in the spleen?

A

It usually arises from secondary involvement in the setting of lymphoid or myeloid neoplasms.

DLBCL typically shows masses in the spleen.

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12
Q

What is the consequence of a splenic rupture?

What symptoms are seen?

A

It is a life-threatening cause of hemoperitoneum and hemorrhagic shock.

LUQ pain, left should pain (Kehr sign), signs of peritonitis and hemodynamic instability.

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13
Q

What does the thymus arise from?

A

Medulla is from the 3rd pharyngeal pouch (endoderm); cortex is from the pharyngeal cleft (ectoderm).

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14
Q

What causes the thymus to involute?

A

Age is the main reason, but it can involute with stress and HIV infection.

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15
Q

What is the size of a thymic cyst?

What is it made of?

A

Usually < 4 cm. They are uncommon and often found incidentally.

Stratified squamous to columnar epithelium surrounding serous or mucinous contents.

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16
Q

What is the major association to make with thymic hyperplasia?

A

Myasthenia gravis (55-60%)

17
Q

What cells make up a thymoma?

What age is common?

What symptoms may occur?

What is the prognosis?

A

Thymic epithelial cells.

> 40 y/o; M=F.

40% have symptoms from impingement of structures.
30-45% present with MG (these tend to benign)
It may be associated with other paraneoplastic syndromes.

> 90% 5-year survival with minimal invasion and complete excision.
<50% 5-year survival with extensive invasion (often metastatic).

18
Q

What are the 3 types of thymoma?

A

Cytologically benign and non-invasive.

Cytologically benign but invasive (metastatic) - penetrates the capsule.

Cytologically malignant (thymic carcinoma).

19
Q

What is the gross appearance of a thymoma?

A

They form firm, lobulated, gray-white masses and measure up to 15-20 cm. They are often encapsulated.

20
Q

What are the 2 types of malignant thymoma?

A

Type 1 (invasive thymoma): cytologically bland but aggressive.

  • most commonly of the cortical-type.
  • 20-25% of all thymomas.

Type 2 (thymic carcinoma): cytologically malignant.

  • most are squamous cell carcinomas.
  • also can be lymphoepithelioma-like carcinoma (associated with EBV).