Literature DB >> 116506

Fibrous lesions in the lower extremities in neurofibromatosis.

G A Mandell, M K Dalinka, B G Coleman.   

Abstract

Multiple fibrous lesions have been noted in the lower extremities of patients with neurofibromatosis (Recklinghausen's disease). These lesions are probably a combination of fibrous cortical defects, nonossifying fibromas, and intraosseous neurofibromas. When several fibrocystic lesions frequent the knee areas in an adolescent, neurofibromatosis should be suspected.

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Year:  1979        PMID： 116506     DOI： 10.2214/ajr.133.6.1135

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN： 0361-803X            Impact factor:   3.959


  6 in total

1.  Whole-body MRI in neurofibromatosis: incidental findings and prevalence of scoliosis.

Authors:  Jacob L Jaremko; Peter J MacMahon; Martin Torriani; Vanessa L Merker; Victor F Mautner; Scott R Plotkin; Miriam A Bredella
Journal:  Skeletal Radiol       Date:  2011-12-07       Impact factor: 2.199

2.  Case report 556: Multiple non-ossifying fibromas of long bones in a patient with neurofibromatosis.

Authors:  M L Gross; N Soberman; H D Dorfman; L P Seimon
Journal:  Skeletal Radiol       Date:  1989       Impact factor: 2.199

3.  Multiple skeletal fibroxanthomas: radiologic-pathologic correlation of 72 cases.

Authors:  R P Moser; D E Sweet; D B Haseman; J E Madewell
Journal:  Skeletal Radiol       Date:  1987       Impact factor: 2.199

4.  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

5.  Scintigraphic differentiation of congenital soft-tissue extremity enlargement with Tc-99m DTPA.

Authors:  G A Mandell; C I Scott; H T Harcke; C Sharkey; L Harris
Journal:  Skeletal Radiol       Date:  1989       Impact factor: 2.199

6.  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
  6 in total

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