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Immunopathology. SYLLABUS: RBP( Robbins Basic Pathology ) Chapter : Diseases of immunity. Immunopathology. Polyarteritis nodosa 108a Glomerulonephritis Rheumatic myocarditis 209 Hashimoto thyroidits. Polyarteritis nodosa.
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Immunopathology SYLLABUS: RBP(Robbins Basic Pathology) Chapter: Diseasesof immunity
Immunopathology • Polyarteritis nodosa 108aGlomerulonephritis • Rheumatic myocarditis 209Hashimoto thyroidits
Polyarteritis nodosa • early phase: degeneration of arterial wall with fibrin deposition and partial or complete destruction of external and internal elastic laminae • inflammatory infiltration within and around vessels predominantly composed of PMNs with leukocytoclasia (fragmentation of their nuclei) • intermediate phase: intimal proliferation, thrombosis, and chronic inflammation in vessels and perivascular tissue • healed phase: fibrosis and recanalization
Glomerulonephritis • Possible lesions: • diffusely enlarged hypercellular glomeruli • mesangial cell proliferation • infiltrating leukocytes • lobular accentuation • thickening of glomerular capillary wall
Rheumatic myocarditis • Aschoff bodies: • foci of swollen eosinophilic collagen • surrounded by lymphocytes (primarily T cells), occasional plasma cells, and Anitschkow cells (pathognomonic for RM plump macrophages with abundant cytoplasm and central round-to-ovoid nuclei with the chromatin disposed in a central, slender, wavy ribbon ("caterpillar cells") • larger macrophages become multinucleated to form Aschoff giant cells
Hashimoto thyroidits • lymphocytic infiltration of parenchyma with follicles and prominent germinal centers • plasma cells, histiocytes, and scattered multinucleated giant cells may be present • small, atrophic follicles with widespread Hürthle cell change (epithelial cells distinguished by the presence of abundant eosinophilic, granular cytoplasm) • in about 12% of case extensive fibrosis (fibrous variant)