Literature DB >> 6747795

A 19-year follow-up of multiple juvenile hyaline fibromatosis.

S Woyke, W Domagala, C Markiewicz.   

Abstract

Nineteen years observation of two siblings with multiple juvenile hyaline fibromatosis is presented. This entity was described 14 years ago. It is concluded that this disease can be effectively controlled by surgical excision of all newly discovered subcutaneous tumors.

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Year:  1984        PMID: 6747795     DOI: 10.1016/s0022-3468(84)80192-x

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  5 in total

1.  Juvenile hyaline fibromatosis: focus on radiographic features in adulthood.

Authors:  Samy Slimani; Assia Haddouche; Sabrina Haid; Aicha Ladjouze-Rezig
Journal:  Rheumatol Int       Date:  2010-07-27       Impact factor: 2.631

2.  Identification of 2 novel ANTXR2 mutations in patients with hyaline fibromatosis syndrome and proposal of a modified grading system.

Authors:  Rafael Denadai; Cassio E Raposo-Amaral; Débora Bertola; Chong Kim; Nivaldo Alonso; Thomas Hart; Sangwoo Han; Rafael F Stelini; Celso L Buzzo; Cesar A Raposo-Amaral; P Suzanne Hart
Journal:  Am J Med Genet A       Date:  2012-03-01       Impact factor: 2.802

3.  Juvenile hyaline fibromatosis.

Authors:  Jayashree Krishnamurthy; Bibhas Saha Dalal; Manjunath V Gubanna
Journal:  Indian J Dermatol       Date:  2011-11       Impact factor: 1.494

4.  A proposal for creating a guideline for cancer registration of the fibromatosis, PEComa group, malignant lymphoma In Situ and dendritic cell tumors (III).

Authors:  Changyoung Yoo; Chang Suk Kang; Yoon La Choi; Hye Yoon Kang; Jin Man Kim; Young Hye Koh; Joo Hee Lee; Seung Sook Lee; In Sun Kim; Dong Hoon Kim; Yong Ku Park; Jin Hee Sohn
Journal:  Korean J Pathol       Date:  2012-10-25

5.  Juvenile Hyaline Fibromatosis: Literature Review and a Case Treated With Surgical Excision and Corticosteroid.

Authors:  Omar Braizat; Saif Badran; Atalla Hammouda
Journal:  Cureus       Date:  2020-10-06
  5 in total

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