Literature DB >> 18491373

Systemic calciphylaxis.

Manika Suryadevara1, Scott J Schurman, Steve K Landas, Abraham Philip, Christopher B Gerlach, Trisha Tavares, Abdul-Kader Souid.   

Abstract

An 11-year-old male developed systemic calciphylaxis during induction therapy for acute lymphoblastic leukemia. His predisposing conditions were hypercalcemia, supplements for pamidronate-induced hypocalcemia and hypophosphatemia and renal insufficiency. He died of cardiorespiratory arrest on the 20th day of induction treatment. Autopsy revealed extensive calcium deposits in the heart, lungs and kidneys. He had diffused alveolar damage, acute tubular necrosis, chronic pancreatitis and marked hepatic steatosis. Systemic calcium deposition may progress rapidly in children with hypercalcemia of malignancy. Since pamidronate reduces mineral resorption from tissues, calcium and phosphate replacements increase systemic mineral deposits. Thus, mineral supplements should be considered only to combat symptoms. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18491373     DOI: 10.1002/pbc.21631

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

Review 1.  Calciphylaxis: a review.

Authors:  Cynthia M Magro; Richard Simman; Sarah Jackson
Journal:  J Am Col Certif Wound Spec       Date:  2011-03-27

2.  Pancreatitis associated with calciphylaxis successfully treated with sodium thiosulfate.

Authors:  Aoibheann Flynn; Aine de Bhailis; Ann-Marie Tobin; George Mellotte; Maureen Connolly
Journal:  JAAD Case Rep       Date:  2018-01-16
  2 in total

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