Oncogenic osteomalacia as a harbinger of recurrent osteosarcoma

10Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Discussion. Oncogenic osteomalacia is a rare paraneoplastic syndrome of skeletal demineralization from renal phosphate loss. Patients with this disorder have the characteristic clinical, laboratory, and radiographic findings of hyperphosphaturic osteomalacia. Although the pathophysiology has not yet been clearly delineated, a humoral factor produced by the tumor is suspected to be the cause. Purpose. We report the first case of oncogenic osteomalacia that improved with chemotherapy, discuss this paraneoplastic syndrome, and review the medical literature regarding its etiology.

Cite

CITATION STYLE

APA

Lamont, E. B., Cavaghan, M. K., & Brockstein, B. E. (1999). Oncogenic osteomalacia as a harbinger of recurrent osteosarcoma. Sarcoma, 3(2), 95–99. https://doi.org/10.1080/13577149977712

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free