Literature DB >> 29364448

Infantile myofibromatosis.

Margarita Larralde1,2, Bruno Ferrari1, Juan Pablo Martinez1, María Angélica Fernández Barbieri3, José Higinio Méndez3, José Casas3.   

Abstract

Infantile myofibromatosis is a mesenchymal disorder characterized by the fibrous proliferation of the skin, bone, muscle and viscera. It is the most common fibrous tumor in childhood. We present a newborn with skin and bone disease without visceral involvement, who showed good response to vinblastine and methotrexate. Clinical features, etiology, diagnosis, and treatment are reviewed.

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Year:  2017        PMID： 29364448      PMCID： PMC5786406          DOI： 10.1590/abd1806-4841.20175001

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN： 0365-0596            Impact factor:   1.896


  10 in total

Review 1.  Orbital infantile myofibroma: a case report and clinicopathologic review of 24 cases from the literature.

Authors:  Corey J Mynatt; Kenneth A Feldman; Lester D R Thompson
Journal:  Head Neck Pathol       Date:  2011-04-22

2.  Infantile myofibromatosis with multiple congenital anomalies.

Authors:  Arun C Inamadar; Aparna Palit; S B Athanikar; V V Sampagavi; N S Deshmukh
Journal:  Pediatr Dermatol       Date:  2005 May-Jun       Impact factor: 1.588

3.  Infantile myofibromatosis: report of nine patients.

Authors:  Margarita Larralde; Mariana V Hoffner; Paula Boggio; María Eugenia Abad; Paula C Luna; Noemí Correa
Journal:  Pediatr Dermatol       Date:  2010 Jan-Feb       Impact factor: 1.588

4.  Infantile myofibromatosis as an unusual cause for unilateral atelectasis in an infant.

Authors:  Kenichi Vinzenz Okuda; Guido Fitze; Jessica Pablik; Gabriele Hahn; Meinolf Suttorp; Christian Vogelberg
Journal:  Pediatr Blood Cancer       Date:  2014-01-22       Impact factor: 3.167

5.  Congenital infantile myofibroma causing intrauterine death in a twin.

Authors:  Christina Yi Ling Aye; Steve Gould; S Adeyemi Akinsola
Journal:  BMJ Case Rep       Date:  2011-12-01

6.  Infantile myofibromatosis: a series of 28 cases.

Authors:  Jacob Mashiah; Smail Hadj-Rabia; Anne Dompmartin; Annie Harroche; Etty Laloum-Grynberg; Michèle Wolter; Jean-Claude Amoric; Dominique Hamel-Teillac; Stéphane Guero; Sylvie Fraitag; Christine Bodemer
Journal:  J Am Acad Dermatol       Date:  2014-06-02       Impact factor: 11.527

7.  A recurrent PDGFRB mutation causes familial infantile myofibromatosis.

Authors:  Yee Him Cheung; Tenzin Gayden; Philippe M Campeau; Charles A LeDuc; Donna Russo; Van-Hung Nguyen; Jiancheng Guo; Ming Qi; Yanfang Guan; Steffen Albrecht; Brenda Moroz; Karen W Eldin; James T Lu; Jeremy Schwartzentruber; David Malkin; Albert M Berghuis; Sherif Emil; Richard A Gibbs; David L Burk; Megan Vanstone; Brendan H Lee; David Orchard; Kym M Boycott; Wendy K Chung; Nada Jabado
Journal:  Am J Hum Genet       Date:  2013-05-23       Impact factor: 11.025

8.  Mutations in PDGFRB cause autosomal-dominant infantile myofibromatosis.

Authors:  John A Martignetti; Lifeng Tian; Dong Li; Maria Celeste M Ramirez; Olga Camacho-Vanegas; Sandra Catalina Camacho; Yiran Guo; Dina J Zand; Audrey M Bernstein; Sandra K Masur; Cecilia E Kim; Frederick G Otieno; Cuiping Hou; Nada Abdel-Magid; Ben Tweddale; Denise Metry; Jean-Christophe Fournet; Eniko Papp; Elizabeth W McPherson; Carrie Zabel; Guy Vaksmann; Cyril Morisot; Brendan Keating; Patrick M Sleiman; Jeffrey A Cleveland; David B Everman; Elaine Zackai; Hakon Hakonarson
Journal:  Am J Hum Genet       Date:  2013-05-23       Impact factor: 11.025

9.  Spontaneous remission of solitary-type infantile myofibromatosis.

Authors:  Kazuhiro Kikuchi; Riichiro Abe; Satoru Shinkuma; Erika Hamasaka; Ken Natsuga; Hiroo Hata; Yasuki Tateishi; Masahiko Shibata; Yuki Tomita; Yukiko Abe; Satoru Aoyagi; Makio Mukai; Hiroshi Shimizu
Journal:  Case Rep Dermatol       Date:  2011-08-26

10.  Solitary infantile myofibromatosis in the bones of the upper extremities: Two rare cases and a review of the literature.

Authors:  Weiliang Wu; Jiansong Chen; Xinfang Cao; Min Yang; Jian Zhu; Guoqiang Zhao
Journal:  Oncol Lett       Date:  2013-09-12       Impact factor: 2.967
  10 in total
  1 in total

1.  Expression of Somatostatin Receptor Subtypes (SSTR-1-SSTR-5) in Pediatric Hematological and Oncological Disorders.

Authors:  Kristof Harda; Zsuzsanna Szabo; Eva Juhasz; Balazs Dezso; Csongor Kiss; Andrew V Schally; Gabor Halmos
Journal:  Molecules       Date:  2020-12-07       Impact factor: 4.411
  1 in total

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