Literature DB >> 6625121

Congenital multiple fibromatosis.

J E Dimmick, W S Wood.   

Abstract

We present a case of congenital multiple fibromatosis to illustrate its characteristic clinical and histopathologic features. The importance of recognizing this disorder is emphasized because of its special clinical behavior and prognosis.

Entities:  

Mesh:

Year:  1983        PMID: 6625121     DOI: 10.1097/00000372-198306000-00017

Source DB:  PubMed          Journal:  Am J Dermatopathol        ISSN: 0193-1091            Impact factor:   1.533


  5 in total

1.  Rapid spontaneous regression of multicentric infantile myofibromatosis in the posterior fossa and lumbar vertebra.

Authors:  Tomoru Miwa; Shizuo Oi; Yuichiro Nonaka; Ryo Tamogami; Hikaru Sasaki; Masaharu Akiyama; Yuki Yuza; Kentaro Yokoi; Yuichi Yokokawa; Hiroyuki Ida
Journal:  Childs Nerv Syst       Date:  2010-10-15       Impact factor: 1.475

Review 2.  Intracranial solitary-type infantile myofibromatosis.

Authors:  E Cardia; D Molina; C Zaccone; G la Rosa; P Napoli
Journal:  Childs Nerv Syst       Date:  1993-07       Impact factor: 1.475

Review 3.  Infantile myofibromatosis: a radiological review.

Authors:  J R Soper; M De Silva
Journal:  Pediatr Radiol       Date:  1993

4.  Imaging findings in seven cases of congenital infantile myofibromatosis with cerebral, spinal, or head and neck involvement.

Authors:  Laura Holzer-Fruehwald; Susan Blaser; Andrea Rossi; Julia Fruehwald-Pallamar; Majda M Thurnher
Journal:  Neuroradiology       Date:  2012-11-16       Impact factor: 2.804

5.  Infantile myofibromatosis of the central nervous system.

Authors:  G Tamburrini; M Gessi; C Colosimo; L Lauriola; F Giangaspero; C Di Rocco
Journal:  Childs Nerv Syst       Date:  2003-04-29       Impact factor: 1.475

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.