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Three years old child with juvenile hyaline fibromatosis presenting with rectal bleeding.
Raja, Kapeel; Khan, Mohammad Arsalan; Mubarak, Mohammad; Abbas, Zaigham; Luck, Nasir Hassan; Hassan, Syed Mujahid.
Afiliação
  • Raja K; Department of Hepatogastroenterlogy, Sindh Institute of Urology and Transplantation, Karachi, Pakistan. kapeelraja@yahoo.com
J Pak Med Assoc ; 63(3): 396-8, 2013 Mar.
Article em En | MEDLINE | ID: mdl-23914649
ABSTRACT
Juvenile hyaline fibromatosis is a rare inherited autosomal recessive disorder which is caused by mutation of CMG2 gene on chromosome 4q21. Mutation of this gene protein can disrupt the formation of basement membranes. Hyalinization of various body tissues like skin, joints, and bones leads to development of skin papules, gingival hyperplasia, osteolytic lesions in bones, and joint contractures. We had a case of a 3 years old female child with Juvenile Hyaline Fibromatosis who presented with rectal bleeding. She had a bleeding mucocutaneous lesion in anal canal along with papullonodular lesions on the face, gingival hypertrophy and flexion contractures of small joints of hands and feet. Excision of the anal lesion revealed histopathological features of Juvenile Hyaline Fibromatosis.
Assuntos
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Base de dados: MEDLINE Assunto principal: Síndrome da Fibromatose Hialina / Hemorragia Gastrointestinal Tipo de estudo: Diagnostic_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Síndrome da Fibromatose Hialina / Hemorragia Gastrointestinal Tipo de estudo: Diagnostic_studies Limite: Child, preschool / Female / Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article