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

被引:2
|
作者
Hata, Chiina [1 ]
Fukawa, Yuki [2 ]
Motoi, Toru [3 ]
Kinowaki, Yuko [4 ]
Akashi, Takumi [5 ]
Ohashi, Kenichi [1 ]
Ishikawa, Yudai [6 ]
Waseda, Yuma [6 ]
Fujii, Yasuhisa [6 ]
Kakuta, Ryota [7 ]
Ikeda, Sadakatsu [7 ]
Onishi, Iichiroh [5 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Human Pathol, Tokyo 1138510, Japan
[2] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Oral Pathol, Tokyo 1138510, Japan
[3] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Dept Pathol, Tokyo 1138677, Japan
[4] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Comprehens Pathol, Tokyo 1138510, Japan
[5] Tokyo Med & Dent Univ Hosp, Dept Diagnost Pathol, Tokyo 1138510, Japan
[6] Tokyo Med & Dent Univ Hosp, Dept Urol, Tokyo 1138510, Japan
[7] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Clin Oncol, Tokyo 1138510, Japan
关键词
giant cell tumor of soft tissue; kidney; malignant transformation; RICH UNDIFFERENTIATED CARCINOMA;
D O I
10.3390/diagnostics13040752
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:8
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