Literature DB >> 12789096

Camurati-Engelmann's disease: a case report.

Rosemary Kusaba Byanyima1, Jennifer Batuuka Nabawesi.   

Abstract

Camurati-Engelmann's disease is a rare condition worldwide. No cases have been documented in Uganda. A 26 year old female presented with a history of grinding pain in the limbs for over 20 years. Strong painkillers would temporally relieve the pain. She had an asthenic stature with generalised reduction in muscle bulk. Plain x-rays revealed the characteristic symmetrical thickening and sclerosis of the diaphyses of the appendicular skeleton and skull base, which is pathognomonic of Camurati-Engelmann's disease. Involvement of the metaphyses of these long bones as well as the metacarpal bones makes this an unusual case.

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Mesh:

Year:  2002        PMID: 12789096      PMCID: PMC2141580     

Source DB:  PubMed          Journal:  Afr Health Sci        ISSN: 1680-6905            Impact factor:   0.927


  5 in total

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Authors:  S RIBBING
Journal:  Acta radiol       Date:  1949-06-30       Impact factor: 1.990

3.  Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reports.

Authors:  M Wright; N R Miller; R M McFadzean; P Riordan-Eva; A G Lee; M D Sanders; G G McIlwaine
Journal:  Br J Ophthalmol       Date:  1998-09       Impact factor: 4.638

4.  Diaphyseal medullary stenosis (sclerosis) with bone malignancy (malignant fibrous histiocytoma): Hardcastle syndrome.

Authors:  K I Norton; J M Wagreich; L Granowetter; J A Martignetti
Journal:  Pediatr Radiol       Date:  1996-09

5.  Progessive diaphyseal dysplasia. Review of the literature and report of seven cases in one family.

Authors:  J D Hundley; F C Wilson
Journal:  J Bone Joint Surg Am       Date:  1973-04       Impact factor: 5.284

  5 in total
  5 in total

1.  Ribbing disease.

Authors:  Philson J Mukkada; Teenu Franklin; Rangasami Rajeswaran; Santhosh Joseph
Journal:  Indian J Radiol Imaging       Date:  2010-02

2.  Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.

Authors:  Michael P Whyte; William G Totty; Deborah V Novack; Xiafang Zhang; Deborah Wenkert; Steven Mumm
Journal:  J Bone Miner Res       Date:  2011-05       Impact factor: 6.741

3.  Clinical characteristics and treatment outcomes in Camurati-Engelmann disease: A case series.

Authors:  Yoon-Myung Kim; Eungu Kang; Jin-Ho Choi; Gu-Hwan Kim; Han-Wook Yoo; Beom Hee Lee
Journal:  Medicine (Baltimore)       Date:  2018-04       Impact factor: 1.889

4.  Camurati-Engelmann disease: a case report from sub-Saharan Africa.

Authors:  Amos O Mwasamwaja; Elifuraha W Mkwizu; Elichilia R Shao; Clement F Kalambo; Isaack Lyaruu; Ben C Hamel
Journal:  Oxf Med Case Reports       Date:  2018-07-17

5.  A Rare Case of Ribbing Disease- Diagnosis and Management.

Authors:  M Lokesh; Sundar Suriyakumar
Journal:  J Orthop Case Rep       Date:  2020-07
  5 in total

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