Literature DB >> 6885383

Progressive diaphyseal dysplasia: Camurati-Engelmann's disease.

C Lazzarone, M Cartesegna, M Crova, D Calorio.   

Abstract

The authors have studied two cases of progressive diaphyseal dysplasia (Camurati Engelmann's disease). In one case their investigations included bone marrow pressure tests, phlebography and blood gas analysis of the medullary blood. The BMP was raised, and the phlebogram showed venous stasis. The blood gas analysis revealed reduced oxygenation of the medullary blood. On the hypothesis that the vascular change could be of pathogenetic significance, the authors proceeded in both cases to open the medullary canal. This produced immediate remission of the pain, which still persists in one case after six years, while it lasted for three years in the second case.

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Year:  1983        PMID: 6885383

Source DB:  PubMed          Journal:  Ital J Orthop Traumatol        ISSN: 0390-5489


  2 in total

Review 1.  Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment.

Authors:  K Janssens; F Vanhoenacker; M Bonduelle; L Verbruggen; L Van Maldergem; S Ralston; N Guañabens; N Migone; S Wientroub; M T Divizia; C Bergmann; C Bennett; S Simsek; S Melançon; T Cundy; W Van Hul
Journal:  J Med Genet       Date:  2005-05-13       Impact factor: 6.318

2.  Anterior Total Hip Arthroplasty With Bulk Femoral Head Autograft in a Patient With Camurati-Engelmann Disease.

Authors:  Adam J Taylor; Robert P Runner; Donald B Longjohn; Soheil Najibi
Journal:  Arthroplast Today       Date:  2021-04-14
  2 in total

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