Literature DB >> 15995450

Tumoral calcinosis in infants: a report of three cases and review of the literature.

Sommer Hammoud1, Edward F McCarthy, Kristy Weber.   

Abstract

Tumoral calcinosis is the deposition of calcium crystals and salts in the periarticular soft tissues. It commonly is seen as a complication of renal dialysis or in patients with a hereditary disposition. Occasionally, it is seen as an isolated condition with no known cause. Tumoral calcinosis usually affects adults and rarely, children. This disorder is extremely uncommon in infants. Only 13 cases have been reported. In this study three additional infants with tumoral calcinosis are reported, bringing the total to 16 cases. These 16 cases provide the opportunity to compare tumoral calcinosis in infants (younger than 18 months) with the disease in older patients. Although histologic and radiologic features in infants and adults are identical, some clinical features differ. In almost all infants, the disease develops without any predisposing factors, such as a family history. Surgical removal of lesions in infants is curative. By contrast, lesions in adults tend to recur after surgery.

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Year:  2005        PMID: 15995450

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  5 in total

1.  A rare disorder: tumoral calcinosis and cirrhosis.

Authors:  Seyyed Farshad Allameh; Akram Ghadiri Anari; Mehrnaz Asadi Gharabaghi; Manouchehr Nakhjavani
Journal:  BMJ Case Rep       Date:  2011-08-17

2.  Subscapular tumoral calcinosis in a toddler: case report.

Authors:  Cheryl G Zvaigzne; David J Patton; Harmeet Kaur; Cynthia L Trevenen; Deepak Kaura
Journal:  J Radiol Case Rep       Date:  2012-06-01

3.  A rare disorder: idiopathic tumoral calcinosis.

Authors:  Gulgun Yilmaz Ovali; Serdar Tarhan; Selim Serter; Petek Bayindir; Guvenir Okcu; Peyker Demireli; Yuksel Pabuscu
Journal:  Clin Rheumatol       Date:  2006-03-25       Impact factor: 3.650

Review 4.  Long-term clinical outcome and phenotypic variability in hyperphosphatemic familial tumoral calcinosis and hyperphosphatemic hyperostosis syndrome caused by a novel GALNT3 mutation; case report and review of the literature.

Authors:  Silje Rafaelsen; Stefan Johansson; Helge Ræder; Robert Bjerknes
Journal:  BMC Genet       Date:  2014-09-24       Impact factor: 2.797

5.  Recurrent idiopathic tumoral calcinosis in a child postoperatively.

Authors:  Garrett S Booth; Rukmalee E Vithana; Daphne E DeMello; Gerald A Mandell
Journal:  Radiol Case Rep       Date:  2015-12-07
  5 in total

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