Literature DB >> 17876123

[Familial tumoral calcinosis in three patients in the same family].

Cihangir Yurdoğlu1, Mehmet Uğur Ozbaydar, Müjdat Adaş, Harzem Ozger.   

Abstract

Tumoral calcinosis is a rare condition characterized by large calcific soft tissue deposits occurring predominantly in a periarticular location. Familial tumoral calcinosis was detected in three members of a family, namely, the father and two offsprings. The father underwent many operations since age 10 for occurrences or recurrences of mass lesions in the right posterior elbow, both hips, left gluteal region, and perineal region. His 16-year-old son underwent his first operation at the age of 10 for a lesion in the posterior elbow, which recurred at the same site and required another operation two years later. He underwent subsequent surgeries for lesions that appeared in the right elbow and right dorsal foot. Finally, the 12-year-old daughter was treated with surgery for a lesion in the right dorsal foot. In all the patients, pathologic diagnoses of all surgical specimens were reported as tumoral calcinosis. All had normocalcemia, hyperphosphatemia, and D hypervitaminosis.

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Mesh:

Year:  2007        PMID: 17876123

Source DB:  PubMed          Journal:  Acta Orthop Traumatol Turc        ISSN: 1017-995X            Impact factor:   1.511


  3 in total

Review 1.  Current understanding of the pathogenesis and management of chronic recurrent multifocal osteomyelitis.

Authors:  Polly J Ferguson; Monica Sandu
Journal:  Curr Rheumatol Rep       Date:  2012-04       Impact factor: 4.592

2.  Tc-MDP bone scintigraphy in a case with sporodical tumoral calcinosis.

Authors:  Tulay Kacar Guveli; Mehmet Mulazimoglu; Muge Oner Tamam; Cüneyt Tamam; Tarik Tatoglu; Tevfik Ozpacaci
Journal:  Indian J Nucl Med       Date:  2010-01

3.  Laxative Related Primary Hyperphosphatemic Tumoral Calcinosis Identified by Bone Scintigraphy.

Authors:  Marcus Asokendaran; Nat Patrick Lenzo
Journal:  World J Nucl Med       Date:  2016-09
  3 in total

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