Spleen and Thymus Path Flashcards

1
Q

splenic pulp

A

artery with eccentric collar of T lymphocytes-expands to form lymphoid nodules composed mainly of B cells

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2
Q

red pulp transversed by

A

numerous thin-walled vascular sinusoids, separated by splenic cords or ‘cords of Billroth’

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3
Q

endothelial lining of sinusoids

A

discontinuous-provides passage for blood cells btwn sinusoids and cords

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4
Q

cords of spleen contain

A

labyrinth of macrophages loosely connected through long dendritic processes to create both physical and fxnal filter

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5
Q

spleen 4 fxns that impact disease states

A

1) phagocytosis of blood cells and particulate matter
2) antiboy production
3) hematopoiesis
4) sequestration of formed blood elements

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6
Q

platelets and speen

A

normally harbors 30-40% total platelet mass; with splenomegaly up to 80-90% platelet mass can be sequestered in interstices of red pulp producing thrombocytopenia

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7
Q

main bacteria patients susceptible to after splenectomy

A

pneumococcus, meningococcus, and Haemophilus influenzae

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8
Q

hypersplenism

A

anemia, leukopenia, thrombocytopenia, alone or in combination; likely due to sequestration and enhanced phagocytosis

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9
Q

nonspecific acute splenitis

A

occurs in any blood-borne infection

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10
Q

nonspecific acute splenitis morphology

A

acute congestion of red pulp which may encroach on and virtually eface the lymphoid follicles

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11
Q

congestive splenomegaly

A

chromic venous outflow obstruction-intrahepatic disorders, extrahepatic disorders impinging on portal or splenic veins, cardiac decompensation, pulmonary

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12
Q

congestive splenomegaly morphology

A

firm, capsule thickened and fibrous; red pulp congested early, but increasingly fibrotic and cellular with time

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13
Q

bland infarcts of spleen

A

pale, wedge-shaped, subcapsular in location; overlying capsule often covered with fibrin

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14
Q

septic infarcts of spleen

A

dvlp suppurative necrosis-in course of healing large, depressed scars often dvlp

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15
Q

most common neoplasm ariseing in spleen

A

lymphangiomas and hemagiomas-often cavernous type

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16
Q

accessory spleens

A

20-35% postmortem exams; small, spherical structures histologically identical to normal spleen

17
Q

where are accessory spleens found

A

within abdominal cavity

18
Q

most common predisposing factor to splenic rupture

A

mono, malaria, typhoid fever, lymphoid neoplasms

19
Q

thymus dvlps from

A

3rd and inconstantly 4th pair of pharyngeal pouches

20
Q

cortical. Epithelial, and peripheral cells in thymus

A

polygonal in shape and have abundant cytoplasm with dendritic extensions that contact adjacent cells

21
Q

epithelial cells in medulla of thymus

A

densely packed, often spindle-shaped, and have scant cytoplasm devoid of interconnecting processes

22
Q

myoid cells

A

muscle-like; may play role in myasthenia gravis

23
Q

DiGerorge syndrome

A

thymic hypoplasia/aplasia, variable parathyroid dvlp associations; 22q11 deletion syndrome

24
Q

thymic cysts

A

usually discovered incidentally

25
Q

thymic follicular hyperplasia

A

appearance of B-cell germinal centers within thymus

26
Q

when is thymic hyperplasia most commonly seen

A

myasthenia gravis (65-75% cases); sometimes Graves’, Lupus, scleroderma, RA, and other autoimmune diseases

27
Q

thymomas

A

tumor of thymic epithelial cells

28
Q

3 histological subtypes of thymomas

A

1) clinically benign and noninvasive

2) benign, but invasive/metastatic 3) cytologically malignant

29
Q

morphology of thymoma

A

lobulated, firm, gray-white masses up to 15-20 cm; sometimes areas of cystic necrosis and calcification; most encapsulated

30
Q

noninvasive thymomas

A

medullary-type epithelial cells or mixture with cortical-type epithelial cells; 50% thymomas

31
Q

invasive thymoma

A

cytologically benign, locally invasive; usually cortical variety with abundant cytoplasm and rounded vesicular nuclei; 20-25% thymomas

32
Q

thymic carcinoma

A

5% thymomas; usually fleshy, most squamous cell carcinomas,

33
Q

lymphoepithelioma-like carcinoma

A

rare thymic carcinoma with sheets of cells with indistinct borders-close histological resemblance to nasopharyngeal carcinoma; 50% EBV