Phosphaturic mesenchymal tumor with symptoms related to osteomalacia that appeared one year after tumorectomy

31Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.

Abstract

A 45-year-old man was admitted to our hospital because of bone pain and hypophosphatemia. He had undergone surgery 2 years previously for a "benign unclassified mesenchymal tumor" in the skull, but there were no clinical symptoms related to osteomalacia. His laboratory examination revealed low serum phosphate, high alkaline phosphatase, and normal calcium levels. The diagnosis of tumor-induced osteomalacia due to phosphaturic mesenchymal tumor mixed connective tissue variant (PMTMCT) was made by re-examining the pathologic specimens. Oral supplementation with phosphate and 1-25-dihydroxyvitamin D relieved his clinical symptoms and laboratory values returned to normal. However, subcutaneous administration of octreotide had no clinical effect. Clinicians and pathologists should be aware of the existence of PMTMCT especially nonphosphaturic or asymptomatic variants of this disorder. © 2006 The Japanese Society of Internal Medicine.

Cite

CITATION STYLE

APA

Yoshioka, K., Nagata, R., Ueda, M., Yamaguchi, T., Konishi, Y., Hosoi, M., … Sato, T. (2006). Phosphaturic mesenchymal tumor with symptoms related to osteomalacia that appeared one year after tumorectomy. Internal Medicine, 45(20), 1157–1160. https://doi.org/10.2169/internalmedicine.45.1797

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