Literature DB >> 3039595

[Neurofibromatosis and multiple nonossifying bone fibromas].

R Erlemann, A R Fischedick, G Edel, P E Peters, M Galanski.   

Abstract

Three patients with a combination of neurofibromatosis and multiple non-ossifying fibromas are presented. All patients possessed multiple osteolytic lesions with sclerotic margins, resembling non-ossifying fibromas. Two patients showed similar lesions in additional localizations. In two patients, non-ossifying fibroma was histologically verified. The simultaneous occurrence of neurofibromatosis and multiple non-ossifying fibromas can possibly be put down to a generalized mesodermal dysplasia. However, the definite explanation is unknown.

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Year:  1987        PMID: 3039595     DOI: 10.1055/s-2008-1048583

Source DB:  PubMed          Journal:  Rofo        ISSN: 1438-9010


  3 in total

1.  Multiple, symmetrical non-ossifying fibromata without extraskeletal anomalies: report of two related cases.

Authors:  K Kozlowski; C Harrington; R Lees
Journal:  Pediatr Radiol       Date:  1993

2.  Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case Report With Literature Survey.

Authors:  Reinhard E Friedrich; Jozef Zustin; Andreas M Luebke; Thorsten Rosenbaum; Martin Gosau; Christian Hagel; Felix K Kohlrusch; Ilse Wieland; Martin Zenker
Journal:  In Vivo       Date:  2021 May-Jun       Impact factor: 2.155

3.  Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.

Authors:  Silvia Vannelli; Raffaele Buganza; Federica Runfola; Ilaria Mussinatto; Antonio Andreacchio; Luisa de Sanctis
Journal:  Ital J Pediatr       Date:  2020-05-11       Impact factor: 2.638

  3 in total

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