Diagnosis of phosphaturic mesenchymal tumor (mixed connective tissue type) by cytopathology
Version of Record online: 14 FEB 2011
Copyright © 2011 Wiley Periodicals, Inc.
Special Issue: Bone and Soft Tissue
Volume 40, Issue S2, pages E109–E113, August 2012
How to Cite
William, J., Laskin, W., Nayar, R. and de Frias, D. (2012), Diagnosis of phosphaturic mesenchymal tumor (mixed connective tissue type) by cytopathology. Diagn. Cytopathol., 40: E109–E113. doi: 10.1002/dc.21647
- Issue online: 27 AUG 2012
- Version of Record online: 14 FEB 2011
- Manuscript Accepted: 9 DEC 2010
- Manuscript Received: 21 OCT 2010
- oncogenic osteomalacia;
- phosphaturic mesenchymal tumor;
- fine-needle aspiration;
- core biopsy
Oncogenic osteomalacia (OO) is a rare paraneoplastic condition in which a bone or soft tissue tumor induces biochemical and clinical signs and symptoms of osteomalacia (or rickets) most often by the production of the phosphaturic protein, fibroblast growth factor-23. Phosphaturic mesenchymal tumor, mixed connective tissue type (PMTMCT) is a rare, histologically distinct tumor that represents the most common cause of OO. As the clinical diagnosis of OO is typically suspected on the basis of clinical and biochemical features and the presence of a bone or soft tissue tumor, cytologic examination might potentially provide the necessary pathologic confirmation of OO. In this case of a 46-year-old female with clinical stigmata of OO and a right distal humeral mass, we report that the fine-needle aspiration findings of short, cytologically bland spindled cells embedded in a fine, fibrillary stromal-rich matrix and the presence of osteoclast-type giant cells associated with the stromal matrix provide strong pathological evidence for PMTMCT and assist in pathologically confirming the clinical impression of OO, thus alleviating the need for a more invasive diagnostic surgical procedure Diagn. Cytopathol. 2012. © 2011 Wiley Periodicals, Inc.