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2.
Am J Surg Pathol ; 31(3): 481-5, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17325492

RESUMO

Crystal-storing histiocytosis is a rare diagnosis that to date has only been associated with 2 conditions: intracytoplasmic accumulation of crystallized immunoglobulins in patients with lymphoproliferative disorders or plasma cell dyscrasias, and histiocytic accumulations of phagocytosed clofazimine, a drug used to treat lepromatous leprosy. We describe a 78-year-old woman with a past medical history of dermatologic mastocytosis and peripheral eosinophilia who presented with diarrhea and weight loss, and was found at colonoscopy to have polyposis limited to the right and transverse colon. She eventually underwent subtotal colectomy to remove the segment of polyposis. At gross examination, the colonic mucosa contained numerous polyps ranging from 1 to 7 mm which on histologic evaluation proved to represent mucosal and submucosal collections of histiocytes whose cytoplasm was distended by numerous brightly eosinophilic crystals. An intense eosinophilic infiltrate surrounded the histiocyte collections and also mildly involved the intervening colonic mucosa and superficial submucosa. Electron microscopy confirmed the presence of intracytoplasmic material identical to Charcot-Leyden crystals within histiocytes, representing the breakdown products of degranulated eosinophils. This is the first reported case of crystal-storing histiocytosis produced by massive accumulation of Charcot-Leyden crystals in eosinophilic colitis.


Assuntos
Colite/patologia , Colo/patologia , Eosinofilia/patologia , Histiocitose/patologia , Corpos de Inclusão/patologia , Polipose Intestinal/patologia , Idoso , Degranulação Celular , Colite/complicações , Colonoscopia , Cristalização , Eosinofilia/complicações , Eosinófilos/ultraestrutura , Feminino , Histiocitose/complicações , Humanos , Corpos de Inclusão/ultraestrutura , Polipose Intestinal/complicações , Macrófagos/patologia , Microscopia Eletrônica de Transmissão
3.
Cutis ; 21(6): 806-10, 1978 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-657838

RESUMO

Erythema nodosum is not an uncommon dermatologic entity. Sarcoidosis and streptococcal infection have become the two most common causes, while tuberculosis was the predominant etiology prior to the use of isoniazid. Histoplasmosis and coccidioidomycosis are two important geographic considerations. Laboratory tests should include a PPD test, chest x-ray, throat culture for beta-streptococcus, and ASO titer determination as a minimum. Symptomatic treatment remains unsatisfactory in many cases, although recent success has been reported with oral potassium iodide.


Assuntos
Eritema Nodoso/etiologia , Infecções Bacterianas/complicações , Colite/complicações , Diagnóstico Diferencial , Eritema Nodoso/diagnóstico , Eritema Nodoso/terapia , Humanos , Hanseníase/complicações , Prognóstico , Tuberculose/complicações
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