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Asghar AM, Uhlman MA, Dahmoush L, et al. Osseous Metaplasia in Mucinous Tubular and Spindle Cell Carcinoma of the Kidney: A Case of Massive, Bilateral Tumors. Case Rep Urol. 2015;2015:465450doi: 10.1155/2015/465450.
Asghar, A. M., Uhlman, M. A., Dahmoush, L., & Deorah, S. (2015). Osseous Metaplasia in Mucinous Tubular and Spindle Cell Carcinoma of the Kidney: A Case of Massive, Bilateral Tumors. Case reports in urology, 2015465450. https://doi.org/10.1155/2015/465450
Asghar, Aeen M, et al. "Osseous Metaplasia in Mucinous Tubular and Spindle Cell Carcinoma of the Kidney: A Case of Massive, Bilateral Tumors." Case reports in urology vol. 2015 (2015): 465450. doi: https://doi.org/10.1155/2015/465450
Asghar AM, Uhlman MA, Dahmoush L, Deorah S. Osseous Metaplasia in Mucinous Tubular and Spindle Cell Carcinoma of the Kidney: A Case of Massive, Bilateral Tumors. Case Rep Urol. 2015;2015:465450. doi: 10.1155/2015/465450. Epub 2015 Aug 12. PMID: 26347846; PMCID: PMC4549541.
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Case Rep Urol. 2015;2015:465450. doi: 10.1155/2015/465450. Epub 2015 Aug 12.

Osseous Metaplasia in Mucinous Tubular and Spindle Cell Carcinoma of the Kidney: A Case of Massive, Bilateral Tumors.

Case reports in urology

Aeen M Asghar, Matthew A Uhlman, Laila Dahmoush, Sundeep Deorah

Affiliations

  1. Carver College of Medicine, University of Iowa, 375 Newton Road, Iowa City, IA 52242, USA.
  2. Department of Urology, University of Iowa, 200 Hawkins Drive, 3 Roy Carver Pavilion, Iowa City, IA 52242-1089, USA.
  3. Department of Pathology, University of Iowa, 200 Hawkins Drive, 5 Roy Carver Pavilion, Iowa City, IA 52242-1089, USA.

PMID: 26347846 PMCID: PMC4549541 DOI: 10.1155/2015/465450

Abstract

Renal cell carcinoma (RCC) is the most common kidney malignancy, with many histologic subtypes. One of the rare forms of RCC is mucinous tubular and spindle cell carcinoma (MTSCC), which is newly described with limited information on clinical picture and outcome. Heterotopic bone formation (osseous metaplasia) is a rare finding within any renal mass. Here we report a case of a massive, bilateral MTSCC with histologic findings of heterotopic bone formation, which has not been described before.

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