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1.
Indian J Pathol Microbiol ; 2014 Jan-Mar 57 (1): 127-129
Artigo em Inglês | IMSEAR | ID: sea-155987

RESUMO

Skin is one of the important organs affected by amyloidosis which is characterized by extracellular deposition of fibrillary proteins having homogenous, eosinophilic on routine staining with distinct tinctorial properties. Nodular cutaneous amyloidosis is rare and may affect dermis, subcutis and also vascular walls. Nodular amyloid deposits in the deeper dermis occurring at the site of insulin injection are a rare observation, which is described here. This description indicates that cutaneous amyloidosis may be associated with local subcutaneous injections of insulin and may clinically mimic a neoplasm or lipodystrophic lesion.

2.
Indian J Pediatr ; 2002 May; 69(5): 437-9
Artigo em Inglês | IMSEAR | ID: sea-78565

RESUMO

Glial choristoma is a developmental malformation of heterotopic central nervous tissue with limited growth potential. It is considered to be one of the very rare choristomatous lesions involving the oral cavity. This report details the morphological characteristics of glial choristoma arising from the palate in a newborn. Bulk of the tissue comprised of mature neuroglial tissue with astrocytes representing developing brain, cystic spaces lined by cuboidal epithelium indicating ependymal layer. Clinical features, associated malformations and histomorphology of this lesion is discussed.


Assuntos
Encéfalo , Coristoma/diagnóstico , Diagnóstico Diferencial , Feminino , Humanos , Recém-Nascido , Doenças da Boca/diagnóstico , Neuroglia
3.
Indian J Pediatr ; 2001 Aug; 68(8): 787-9
Artigo em Inglês | IMSEAR | ID: sea-81960

RESUMO

Klippel Trenaunay syndrome is a rare congenital disorder characterised by vascular anomalies and life threatening complications. Clinical recognition, prenatal diagnosis and counselling is important in these cases. Here we present a case of Klippel-Trenaunay syndrome and emphasize upon the clinical significance of such cases.


Assuntos
Autopsia , Doenças Fetais/patologia , Humanos , Síndrome de Klippel-Trenaunay-Weber/congênito , Masculino
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