Literature DB >> 2458083

Juvenile hyaline fibromatosis. A histologic and histochemical study.

A Mayer-da-Silva1, A Poiares-Baptista, F Guerra Rodrigo, M Teresa-Lopes.   

Abstract

Histochemical and routine light microscopic studies were performed in nodular skin lesions excised from one patient with juvenile hyaline fibromatosis. The lesions had different times of evolution. Recent lesions showed a high density of fibroblastlike cells embedded in an amorphous matrix of glycoproteins, hyaluronic acid, and small amounts of chondroitin sulfates A and C and of dermatan sulfate. The progressive enlargement of the lesions was due to an increase in the amount of intercellular matrix produced by the cells that progressively displayed a pattern of peripheral stratification. In the older lesions, the matrix was mainly composed by chondroitin sulfates A and C. We suggest that juvenile hyaline fibromatosis represents a disease of the connective tissue with progressive abnormal differentiation to chondroid tissue.

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Year:  1988        PMID: 2458083

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  7 in total

1.  [Juvenile hyaline fibromatosis].

Authors:  K Güldner; C Hendricks; J Schaller; J Kunze
Journal:  Hautarzt       Date:  2009-09       Impact factor: 0.751

Review 2.  The dark sides of capillary morphogenesis gene 2.

Authors:  Julie Deuquet; Ekkehart Lausch; Andrea Superti-Furga; F Gisou van der Goot
Journal:  EMBO J       Date:  2011-12-06       Impact factor: 11.598

3.  Infantile Systemic Hyalinosis: Novel Founder Mutation in the Initiation Codon among "Malis (Farmers)" in Jodhpur.

Authors:  Jai Prakash Soni; Ratna D Puri; Kapil Jetha; G S L Bhavani; Monika Chaudhary; Sudha Kohli; I C Verma
Journal:  Indian J Pediatr       Date:  2016-10-18       Impact factor: 1.967

4.  Infantile systemic hyalinosis: Report of two severe cases from Saudi Arabia and review of the literature.

Authors:  Sahar Ahmed Fathi Hammoudah; Lama Mohammed El-Attar
Journal:  Intractable Rare Dis Res       Date:  2016-05

5.  Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

Authors:  Sandra Hanks; Sarah Adams; Jenny Douglas; Laura Arbour; David J Atherton; Sevim Balci; Harald Bode; Mary E Campbell; Murray Feingold; Gökhan Keser; Wim Kleijer; Grazia Mancini; John A McGrath; Francesco Muntoni; Arti Nanda; M Dawn Teare; Matthew Warman; F Michael Pope; Andrea Superti-Furga; P Andrew Futreal; Nazneen Rahman
Journal:  Am J Hum Genet       Date:  2003-08-21       Impact factor: 11.025

6.  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

7.  Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report.

Authors:  Imane Cherkaoui Jaouad; Soukaina Guaoua; Aicha Hajjioui; Abdelaziz Sefiani
Journal:  J Med Case Rep       Date:  2014-09-03
  7 in total

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