Juvenile hyaline fibromatosis
JPMI-Journal of Postgraduate Medical Institute. 2013; 27 (1): 105-107
em Inglês
| IMEMR
| ID: emr-130437
ABSTRACT
Juvenile hyaline fibromatosis is a rare, autosomal recessive disease. We report a 4-year-old female born of first-degree consanguineous marriage, presenting with gingival hyperplasia, nodular swellings involving the both pinna and right ankle joint. She had contractures of elbows, knees and shoulder joints, restricting the movements of these joints. Cutaneous examination revealed erythematous papules and plaques involving the nape of neck and the perianal region. Histological examination revealed deposition of PAS positive amorphous eosinophilic hyaline material with scattered intervening fibroblast like cells resembling chondroid cells. The patient was diagnosed as a case of Juvenile hyaline fibromatosis based on characteristic clinical and histopathological findings:
Buscar no Google
Índice:
IMEMR (Mediterrâneo Oriental)
Assunto principal:
Hiperplasia Gengival
/
Doenças Genéticas Inatas
Tipo de estudo:
Relato de Casos
Limite:
Feminino
/
Humanos
Idioma:
Inglês
Revista:
J. Postgrad. Med. Inst.
Ano de publicação:
2013
Similares
MEDLINE
...
LILACS
LIS