Literature DB >> 7211781

Tumoral calcinosis in an infant.

B Bostrom.   

Abstract

Tumoral calcinosis is a disease characterized by large, calcified, painless masses, usually near joints, in otherwise healthy children and young adults. Biochemical findings are normal except for an association with hyperphosphatemia. A familial and racial predisposition is seen, with most cases affecting blacks. This disease is believed to represent an unknown inherited abnormality in phosphate metabolism. Because of the tendency of the masses to recur after incomplete excision, the recommended treatment is early and complete excision. Phosphate binders may be useful in certain cases.

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Year:  1981        PMID: 7211781     DOI: 10.1001/archpedi.1981.02130270038013

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  6 in total

1.  Tumoral calcinosis revisited--common and uncommon features. Report of ten cases and review.

Authors:  A Metzker; B Eisenstein; J Oren; R Samuel
Journal:  Eur J Pediatr       Date:  1988-02       Impact factor: 3.183

2.  Tumoral calcium pyrophosphate deposition disease.

Authors:  H A Sissons; G C Steiner; F Bonar; M May; Z S Rosenberg; H Samuels; D Present
Journal:  Skeletal Radiol       Date:  1989       Impact factor: 2.199

3.  Tumoral calcinosis in an infant.

Authors:  S B Greenberg
Journal:  Pediatr Radiol       Date:  1990

Review 4.  Tumoral calcinosis: case report and review.

Authors:  A F Bishop; J M Destouet; W A Murphy; L A Gilula
Journal:  Skeletal Radiol       Date:  1982       Impact factor: 2.199

5.  Tumoral calcinosis: radiologic-pathologic correlation.

Authors:  L S Steinbach; J O Johnston; E F Tepper; G D Honda; W Martel
Journal:  Skeletal Radiol       Date:  1995-11       Impact factor: 2.199

6.  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
  6 in total

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