Literature DB >> 15953379

Juvenile hyaline fibromatosis: a case report.

Naci Karaçal1, Nevzat Gülçelik, Kadriye Yildiz, Sevdegül Mungan, Necmettin Kutlu.   

Abstract

Juvenile hyaline fibromatosis ( JHF ) is a rare autosomal recessive disease characterized by papulonodular skin lesions, gingival hyperplasia, joint contractures, and bone lesions. The skin lesions may consist of multiple large tumors, commonly on the scalp and around the neck, and small pearly, pink papules and plaques on the trunk, chin, ears, and around the nostrils. Here, we report a 2-year-old boy with characteristic stiffness of the knees and elbows and pink confluent papules on the paranasal folds, and periauricular and perianal regions. He also had hard nodules all over the scalp and around the mouth, and severe gingival hyperplasia. The lesions were totally excised and clinicopathological diagnosis was JHF.

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Year:  2005        PMID: 15953379     DOI: 10.1111/j.0303-6987.2005.00341.x

Source DB:  PubMed          Journal:  J Cutan Pathol        ISSN: 0303-6987            Impact factor:   1.587


  2 in total

1.  Juvenile Hyaline Fibromatosis: A 10-year Follow-up.

Authors:  Esra Baltacioglu; Esra Guzeldemir; Erkan Sukuroglu; Kadriye Yildiz; Pinar Yuva; Güven Aydin; Naci Karacal
Journal:  Indian J Dermatol       Date:  2017 Mar-Apr       Impact factor: 1.494

2.  Ultrasound findings in infantile systemic hyalinosis.

Authors:  José Alexandre Mendonça; Roberto Marini; Nadia Bossolan Schincariol; Ieda Maria Magalhães Laurindo; Simone Appenzeller
Journal:  Rheumatol Int       Date:  2010-12-09       Impact factor: 2.631

  2 in total

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