Hypocalcemia in a patient with osteosarcoma and 22q11.2 deletion syndrome

Hypocalcemia is a rare complication of osteosarcoma, having been described in only 4 reports. We present the case of a 16-year-old male with metastatic osteosarcoma of the right humerus who was found to have severe asymptomatic hypocalcemia. Cytogenetic analysis of peripheral blood revealed a microd...

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Veröffentlicht in:Journal of pediatric hematology/oncology 2008-08, Vol.30 (8), p.612-617
Hauptverfasser: Mussai, Francis J, Cunningham, Lea C, Rezvani, Geoffrey, Stratakis, Constantine A, Reynolds, James C, Nesterova, Galina, Henshaw, Robert M, Levine, Jason E, Helman, Lee J, Arthur, Diane C, Kim, Su Young
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Sprache:eng
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Zusammenfassung:Hypocalcemia is a rare complication of osteosarcoma, having been described in only 4 reports. We present the case of a 16-year-old male with metastatic osteosarcoma of the right humerus who was found to have severe asymptomatic hypocalcemia. Cytogenetic analysis of peripheral blood revealed a microdeletion in band 22q11.2. Following amputation of the tumor-bearing extremity, the patient's calcium levels increased, but did not normalize. These findings suggested that the etiology of his hypocalcemia was osteoblastic utilization of calcium by the tumor, exacerbated by 22q11.2 deletion syndrome.
ISSN:1077-4114
1536-3678
DOI:10.1097/MPH.0b013e318168f072