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34 Cards in this Set
- Front
- Back
spleen specs |
150 g; enclosed in thin, glistening, slate-gray CT capsule; extenisve red pulp dotted with gray specs (white pulp follicles) |
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splenic pulp
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artery with eccentric collar of T lymphocytes-expands to form lymphoid nodules composed mainly of B cells |
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red pulp transversed by
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numerous thin-walled vascular sinusoids, separated by splenic cords or 'cords of Billroth' |
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endothelial lining of sinusoids
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discontinuous-provides passage for blood cells btwn sinusoids and cords
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cords of spleen contain
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labyrinth of macrophages loosely connected through long dendritic processes to create both physical and fxnal filter |
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spleen 4 fxns that impact disease states
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1) phagocytosis of blood cells and particulate matter 2) antiboy production 3) hematopoiesis 4) sequestration of formed blood elements |
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platelets and speen
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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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main bacteria patients susceptible to after splenectomy
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pneumococcus, meningococcus, and Haemophilus influenzae |
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hypersplenism
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anemia, leukopenia, thrombocytopenia, alone or in combination; likely due to sequestration and enhanced phagocytosis |
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nonspecific acute splenitis
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occurs in any blood-borne infection |
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nonspecific acute splenitis morphology
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acute congestion of red pulp which may encroach on and virtually eface the lymphoid follicles |
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congestive splenomegaly
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chromic venous outflow obstruction-intrahepatic disorders, extrahepatic disorders impinging on portal or splenic veins, cardiac decompensation, pulmonary |
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congestive splenomegaly morphology
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firm, capsule thickened and fibrous; red pulp congested early, but increasingly fibrotic and cellular with time |
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bland infarcts of spleen
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pale, wedge-shaped, subcapsular in location; overlying capsule often covered with fibrin |
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septic infarcts of spleen
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dvlp suppurative necrosis-in course of healing large, depressed scars often dvlp |
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most common neoplasm ariseing in spleen
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lymphangiomas and hemagiomas-often cavernous type
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accessory spleens
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20-35% postmortem exams; small, spherical structures histologically identical to normal spleen |
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where are accessory spleens found
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within abdominal cavity
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most common predisposing factor to splenic rupture
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mono, malaria, typhoid fever, lymphoid neoplasms |
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thymus dvlps from
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3rd and inconstantly 4th pair of pharyngeal pouches |
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cortical. Epithelial, and peripheral cells in thymus
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polygonal in shape and have abundant cytoplasm with dendritic extensions that contact adjacent cells
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epithelial cells in medulla of thymus
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densely packed, often spindle-shaped, and have scant cytoplasm devoid of interconnecting processes |
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myoid cells
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muscle-like; may play role in myasthenia gravis |
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DiGerorge syndrome
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thymic hypoplasia/aplasia, variable parathyroid dvlp associations; 22q11 deletion syndrome
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thymic cysts
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usually discovered incidentally
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thymic follicular hyperplasia
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appearance of B-cell germinal centers within thymus
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when is thymic hyperplasia most commonly seen
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myasthenia gravis (65-75% cases); sometimes Graves', Lupus, scleroderma, RA, and other autoimmune diseases
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thymomas
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tumor of thymic epithelial cells
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3 histological subtypes of thymomas
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1) clinically benign and noninvasive 2) benign, but invasive/metastatic 3) cytologically malignant
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morphology of thymoma
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lobulated, firm, gray-white masses up to 15-20 cm; sometimes areas of cystic necrosis and calcification; most encapsulated
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noninvasive thymomas
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medullary-type epithelial cells or mixture with cortical-type epithelial cells; 50% thymomas
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invasive thymoma
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cytologically benign, locally invasive; usually cortical variety with abundant cytoplasm and rounded vesicular nuclei; 20-25% thymomas
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thymic carcinoma
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5% thymomas; usually fleshy, most squamous cell carcinomas,
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lymphoepithelioma-like carcinoma
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rare thymic carcinoma with sheets of cells with indistinct borders-close histological resemblance to nasopharyngeal carcinoma; 50% EBV
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