Juvenile hyaline fibromatosis: a case report.
Pathologica
; 106(2): 70-2, 2014 Jun.
Article
em En
| MEDLINE
| ID: mdl-25291871
ABSTRACT
Juvenile hyaline fibromatosis is a rare, hereditary disease with distinct clinical and histopathological features. Clinically, it presents with gingival hypertrophy, pappulonodular skin lesions and joint contractures. Bone involvement is usually an uncommon finding. We report a case of a 2-year-old patient, daughter of consanguineous parents, who presented since the age of 2 months with impairment of mental development, multiple joint contractures, motion limitation and nodules on the scalp. The calvarian lesions were surgically removed, and histopathological examination concluded to juvenile hyaline fibromatosis.
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Base de dados:
MEDLINE
Assunto principal:
Síndrome da Fibromatose Hialina
/
Hialina
Tipo de estudo:
Diagnostic_studies
/
Etiology_studies
/
Prognostic_studies
Limite:
Child, preschool
/
Female
/
Humans
Idioma:
En
Ano de publicação:
2014
Tipo de documento:
Article