Literature DB >> 23087282

Pathological fractures on both lower limbs with Jaffe-Campanacci's syndrome.

Mehmet Sonar1, Mustafa Isik, Aslihan Yilmaz Ekmekci, Ozgen Arslan Solmaz.   

Abstract

Jaffe-Campanacci's syndrome is a very rare condition and was first described by Jaffe in 1958. It is presented by non-ossifying fibromas, café-au-lait spots and axillar freckling. Non-ossifying fibromas are usually found after minor traumas or stress fractures. Differential diagnosis to neurofibromatosis include the absence of Lisch granules, neurofibromatous skin lesions and schwannomatous soft tissue masses. In this case, we report a 13-year-old white boy with Jaffe-Campanacci's syndrome, and bilateral pathological lower limbs fracture.

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Year:  2012        PMID: 23087282      PMCID: PMC4543732          DOI: 10.1136/bcr-2012-007047

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  13 in total

Review 1.  Jaffe-Campanacci syndrome. A case report and review of the literature.

Authors:  Mohammad Anwar Hau; Edward J Fox; Justin M Cates; Brian E Brigman; Henry J Mankin
Journal:  J Bone Joint Surg Am       Date:  2002-04       Impact factor: 5.284

2.  On fibrous defects in cortical walls of growing tubular bones: their radiologic appearance, structure, prevalence, natural course, and diagnostic significance.

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Journal:  Adv Pediatr       Date:  1955

3.  Interesting medical images: the Jaffe-Campanacci syndrome.

Authors:  Taxiarchis V Kourelis; Akrivi Manola
Journal:  Conn Med       Date:  2012-05

4.  Fibrous cortical defect and nonossifying fibroma of bone. A study of the ultrastructure.

Authors:  G C Steiner
Journal:  Arch Pathol       Date:  1974-04

Review 5.  Jaffe-Campanacci syndrome: case report and review of literature.

Authors:  D Kotzot; H Stöss; H Wagner; R Ulmer
Journal:  Clin Dysmorphol       Date:  1994-10       Impact factor: 0.816

6.  Multiple non-ossifying fibromata with extraskeletal anomalies: a new syndrome?

Authors:  M Campanacci; M Laus; S Boriani
Journal:  J Bone Joint Surg Br       Date:  1983-11

7.  Neurofibromatosis and multiple nonossifying fibromas.

Authors:  A M Schwartz; R M Ramos
Journal:  AJR Am J Roentgenol       Date:  1980-09       Impact factor: 3.959

8.  Jaffe-Campanacci syndrome.

Authors:  Ammar C Al-Rikabi; Jyothi C Ramaswamy; Venkatraman V Bhat
Journal:  Saudi Med J       Date:  2005-01       Impact factor: 1.484

9.  Pathological fractures through non-ossifying fibromas. Review of the Mayo Clinic experience.

Authors:  M A Arata; H A Peterson; D C Dahlin
Journal:  J Bone Joint Surg Am       Date:  1981-07       Impact factor: 5.284

10.  Is Jaffe-Campanacci syndrome just a manifestation of neurofibromatosis type 1?

Authors:  Randall S Colby; Robert A Saul
Journal:  Am J Med Genet A       Date:  2003-11-15       Impact factor: 2.802

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  3 in total

1.  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

2.  Pathological fracture of non-ossifying fibroma associated with neurofibromatosis type 1.

Authors:  James Ritchie Gill; Tamer Magid El Nakhal; Soo-Mi Park; Mariusz Chomicki
Journal:  BMJ Case Rep       Date:  2019-07-21

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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