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34 Cards in this Set

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spleen specs

150 g; enclosed in thin, glistening, slate-gray CT capsule; extenisve red pulp dotted with gray specs (white pulp follicles)

splenic pulp

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

red pulp transversed by

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

endothelial lining of sinusoids
discontinuous-provides passage for blood cells btwn sinusoids and cords
cords of spleen contain

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

spleen 4 fxns that impact disease states

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

platelets and speen

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

main bacteria patients susceptible to after splenectomy

pneumococcus, meningococcus, and Haemophilus influenzae

hypersplenism

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

nonspecific acute splenitis

occurs in any blood-borne infection

nonspecific acute splenitis morphology

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

congestive splenomegaly

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

congestive splenomegaly morphology

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

bland infarcts of spleen

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

septic infarcts of spleen

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

most common neoplasm ariseing in spleen
lymphangiomas and hemagiomas-often cavernous type
accessory spleens

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

where are accessory spleens found
within abdominal cavity
most common predisposing factor to splenic rupture

mono, malaria, typhoid fever, lymphoid neoplasms

thymus dvlps from

3rd and inconstantly 4th pair of pharyngeal pouches

cortical. Epithelial, and peripheral cells in thymus
polygonal in shape and have abundant cytoplasm with dendritic extensions that contact adjacent cells
epithelial cells in medulla of thymus

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

myoid cells

muscle-like; may play role in myasthenia gravis

DiGerorge syndrome
thymic hypoplasia/aplasia, variable parathyroid dvlp associations; 22q11 deletion syndrome
thymic cysts
usually discovered incidentally
thymic follicular hyperplasia
appearance of B-cell germinal centers within thymus
when is thymic hyperplasia most commonly seen
myasthenia gravis (65-75% cases); sometimes Graves', Lupus, scleroderma, RA, and other autoimmune diseases
thymomas
tumor of thymic epithelial cells
3 histological subtypes of thymomas
1) clinically benign and noninvasive 2) benign, but invasive/metastatic 3) cytologically malignant
morphology of thymoma
lobulated, firm, gray-white masses up to 15-20 cm; sometimes areas of cystic necrosis and calcification; most encapsulated
noninvasive thymomas
medullary-type epithelial cells or mixture with cortical-type epithelial cells; 50% thymomas
invasive thymoma
cytologically benign, locally invasive; usually cortical variety with abundant cytoplasm and rounded vesicular nuclei; 20-25% thymomas
thymic carcinoma
5% thymomas; usually fleshy, most squamous cell carcinomas,
lymphoepithelioma-like carcinoma
rare thymic carcinoma with sheets of cells with indistinct borders-close histological resemblance to nasopharyngeal carcinoma; 50% EBV