A Primary Kidney Giant Cell Tumor of Soft Tissue Caused Peritoneal Dissemination, Considered to Be Malignant Transformation: A Case Report

Author:

Hata Chiina1ORCID,Fukawa Yuki2ORCID,Motoi Toru3ORCID,Kinowaki Yuko4ORCID,Akashi Takumi5,Ohashi Kenichi1,Ishikawa Yudai6ORCID,Waseda Yuma6ORCID,Fujii Yasuhisa6,Kakuta Ryota7,Ikeda Sadakatsu7,Onishi Iichiroh5ORCID

Affiliation:

1. Department of Human Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan

2. Department of Oral Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan

3. Department of Pathology, Tokyo Metropolitan Cancer and Infectious Disease Center, Komagome Hospital, Tokyo 113-8677, Japan

4. Department of Comprehensive Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan

5. Department of Diagnostic Pathology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan

6. Department of Urology, Tokyo Medical and Dental University Hospital, Tokyo 113-8510, Japan

7. Department of Clinical Oncology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan

Abstract

Giant cell tumor of soft tissue (GCTST) is a defined disease entity that has a morphology similar to giant cell tumor of bone (GCTB). The malignant transformation of GCTST has not been reported, and a kidney primary is extremely rare. We report the case of a 77-year-old Japanese male, who was diagnosed with primary GCTST of the kidney and showed peritoneal dissemination, considered to be a malignant transformation of GCTST, in 4 years and 5 months. Histologically, the primary lesion showed characteristics of round cells with not prominent atypia, multi-nucleated giant cells, and osteoid formation, and carcinoma components were not found. The peritoneal lesion was characterized by osteoid formation and round to spindle-shaped cells, but differed in nuclear atypia, and multi-nucleated giant cells were not detected. Immunohistochemical and cancer genome sequence analysis suggested these tumors were sequential. This is a first report of a case that we could diagnose as primary GCTST of the kidney and could be determined as malignant transformation of GCTST in the clinical course. Analysis of this case will be examined in the future when genetic mutations and the disease concepts of GCTST are established.

Publisher

MDPI AG

Subject

Clinical Biochemistry

Reference17 articles.

1. Dilani Lokuhetty, V.A.W., and Cree, I.A. (2020). WHO Classification of Soft Tissue and Bone Tumours, International Agency for Research on Cancer. [5th ed.].

2. Primary de novo malignant giant cell tumor of kidney: A case report;Kanthan;BMC Urol.,2004

3. Osteoclast-rich undifferentiated carcinomas of the urinary tract;Baydar;Mod. Pathol.,2006

4. Clear cell renal cell carcinoma with a syncytial-type multinucleated giant tumor cell component: Implications for differential diagnosis;Williamson;Hum. Pathol.,2014

5. An expanded immunohistochemical profile of osteoclast-rich undifferentiated carcinoma of the urinary tract;Priore;Mod. Pathol.,2018

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