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Leiomyoblastoma Associated With Intractable Hypercalcemia and Elevated 1,25Dihydroxycholecalciferol LevelsTreatment by Hepatic Enzyme Induction
Maximo Maislos, MD;
Richard Sobel, MD;
Shraga Shany, PhD
Arch Intern Med. 1985;145(3):565-567.
Abstract
A 42-year-old woman, with a previously resected jejunal leiomyoblastoma, was first seen with liver metastases 3 years after the tumor resection. Intractable malignant hypercalcemia appeared eight months later, together with renal insufficiency. No osteolytic lesions were detected. Levels of parathyroid hormone, cyclic adenosine monophosphate, and 1,25-dihydroxycholecalciferol (1,25[OH]2D) were not useful in distinguishing between the hypercalcemia of malignancy and concurrent hyperparathyroidism. Despite renal insufficiency, hypercalcemia, and subtotal parathyroidectomy, the 1,25(OH)2D levels remained elevated, consistent with the speculation that a tumor product stimulated 1- -hydroxylation of 25-hydroxycholecalciferol. Phenytoin and phenobarbital (enzyme induction therapy), in combination with phosphorus and glucocorticoids, appeared to be useful in controlling the hypercalcemia.
(Arch Intern Med 1985;145:565-567)
Author Affiliations
From the Department of Medicine (Drs Maislos and Sobel) and the Toor Institute (Dr Shany), Soroka University Hospital and the Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Footnotes
Accepted for publication Nov 29, 1983.
Reprint requests to Department of Medicine, Soroka Medical Center, PO Box 151, Beer-Sheva 84-101, Israel (Dr Sobel).
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