Literature DB >> 29058046

Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis): whole-body MR findings in two siblings with different subcutaneous nodules distribution.

Davide Castiglione1, Maria Chiara Terranova1, Dario Picone1, Giuseppe Lo Re1, Sergio Salerno2.   

Abstract

Hyaline fibromatosis syndrome (juvenile hyaline fibromatosis) is a rare, progressive, autosomal recessive disorder whose main hallmark is the deposition of amorphous hyaline material in soft tissues, with an evolutionary course and health impairment. It may present involvement of subcutaneous or periskeletal soft tissue, or may develop as a visceral infiltration entity with poor prognosis. Very few radiological data about this inherited condition have been reported, due to the extreme rarity of disease. We herein present a case of two siblings, affected by different severity of the disease, with different clinical features. They were examined by whole-body MR (WBMR) in order to assess different lesions localization, to rule out any visceral involvement and any other associated anomalies and to define patients' management.

Entities:  

Keywords:  Fibromatosis; Hyaline; Juvenile; Whole body MR

Mesh:

Year:  2017        PMID: 29058046     DOI: 10.1007/s00256-017-2799-y

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  23 in total

1.  Juvenile hyaline fibromatosis: a rare lesion.

Authors:  Yasmin Altaf Momin; Bhavana Madhukar Bharambe; Grace D'Costa
Journal:  Indian J Pathol Microbiol       Date:  2011 Oct-Dec       Impact factor: 0.740

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

Review 3.  Two siblings with juvenile hyaline fibromatosis: case reports and review of the literature.

Authors:  G Keser; B Karabulut; F Oksel; C Calli; E E Ustün; T Akalin; H Koçanaoğullari; G Gümüdiş; E Doğanavşargil
Journal:  Clin Rheumatol       Date:  1999       Impact factor: 2.980

4.  Juvenile hyaline fibromatosis.

Authors:  A Y Finlay; S D Ferguson; P J Holt
Journal:  Br J Dermatol       Date:  1983-05       Impact factor: 9.302

5.  Radiation dose from multidetector CT studies in children: results from the first Italian nationwide survey.

Authors:  Claudio Granata; Daniela Origgi; Federica Palorini; Domenica Matranga; Sergio Salerno
Journal:  Pediatr Radiol       Date:  2014-11-08

6.  Infantile systemic hyalinosis or juvenile hyaline fibromatosis?

Authors:  Francisco Urbina; Ivo Sazunic; Guillermo Murray
Journal:  Pediatr Dermatol       Date:  2004 Mar-Apr       Impact factor: 1.588

7.  Juvenile hyaline fibromatosis: ultrastructural study.

Authors:  B C Winik; M C Boente; R Asial
Journal:  Am J Dermatopathol       Date:  1998-08       Impact factor: 1.533

Review 8.  Juvenile hyaline fibromatosis: two new patients and review of the literature.

Authors:  M N Fayad; A Yacoub; S Salman; A Khudr; V M Der Kaloustian
Journal:  Am J Med Genet       Date:  1987-01

9.  Systemic hyalinosis (juvenile hyaline fibromatosis). Ultrastructure of the hyaline with particular reference to the cross-banded structure.

Authors:  H Ishikawa; H Maeda; H Takamatsu; Y Saito
Journal:  Arch Dermatol Res       Date:  1979-06-25       Impact factor: 3.017

10.  The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.

Authors:  Nazneen Rahman; Melanie Dunstan; M Dawn Teare; Sandra Hanks; Sarah J Edkins; Jaime Hughes; Graham R Bignell; Grazia Mancini; Wim Kleijer; Mary Campbell; Gokhan Keser; Carol Black; Nigel Williams; Laura Arbour; Matthew Warman; Andrea Superti-Furga; P Andrew Futreal; F Michael Pope
Journal:  Am J Hum Genet       Date:  2002-09-04       Impact factor: 11.025

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  1 in total

Review 1.  Update of pediatric soft tissue tumors with review of conventional MRI appearance-part 1: tumor-like lesions, adipocytic tumors, fibroblastic and myofibroblastic tumors, and perivascular tumors.

Authors:  Jack Porrino; Khalid Al-Dasuqi; Lina Irshaid; Annie Wang; Kimia Kani; Andrew Haims; Ezekiel Maloney
Journal:  Skeletal Radiol       Date:  2021-06-30       Impact factor: 2.199

  1 in total

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