Literature DB >> 8482029

Correlation between bone imaging and the clinical picture in two unsuspected cases of progressive diaphyseal dysplasia (Engelmann's disease).

A D'Addabbo1, L Macarini, G Rubini, D Rubini, F Salzillo, F Lauriero.   

Abstract

Progressive diaphyseal dysplasia was incidentally discovered in two patients referred for Tc-99m MDP bone scintigraphy (one for intense sciatica, the other for the detection of breast cancer metastases). Tracer accumulation in the diaphyses of the lower limbs and the base of the skull was accompanied by bone thickening and patency of the medullary cavity, as demonstrated by radiography, MRI, and bone marrow scanning. Comparison of the clinical pictures with the results of instrumental examinations showed that these were cases of sporadic progressive diaphyseal dysplasia of slight and average gravity, respectively. The differentiation of Ribbing's disease is explained and reference also is made to a finding not mentioned in the literature, namely frontal bone resorption lacunules in one patient.

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Year:  1993        PMID: 8482029     DOI: 10.1097/00003072-199304000-00012

Source DB:  PubMed          Journal:  Clin Nucl Med        ISSN: 0363-9762            Impact factor:   7.794


  2 in total

1.  A significant improvement in lower limb pain after treatment with alendronate in two cases of Camurati-Engelmann disease.

Authors:  Kousuke Iba; Junichi Takada; Hotaka Kamasaki; Takashi Oda; Naoko Hatakeyama; Takuro Wada; Toshihiko Yamashita
Journal:  J Bone Miner Metab       Date:  2008-01-10       Impact factor: 2.626

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

  2 in total

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