Primary Synovial Sarcoma of the Kidney
The case was a 40-year-old female. She visited a local doctor with a chief complaint of right side abdominal pain. A right kidney tumor measuring 10 cm in diameter was observed in an abdominal Computed Tomography (CT) scan. Based on the CT image, the possibility of angiomiolipoma (AML) could not be...
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Format: | Article |
Language: | English |
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Karger Publishers
2009-10-01
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Series: | Case Reports in Oncology |
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Online Access: | http://www.karger.com/Article/FullText/245926 |
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author | Takashi Kawahara Zenkichi Sekiguchi Kazuhide Makiyama Takashi Nakayama Yoji Nagashima Kaoru Kita Kazuhiro Namura Hiroki Itou Futoshi Sano Narihiko Hayashi Noboru Nakaigawa Takehiko Ogawa Hiroji Uemura Masahiro Yao Yoshinobu Kubota |
author_facet | Takashi Kawahara Zenkichi Sekiguchi Kazuhide Makiyama Takashi Nakayama Yoji Nagashima Kaoru Kita Kazuhiro Namura Hiroki Itou Futoshi Sano Narihiko Hayashi Noboru Nakaigawa Takehiko Ogawa Hiroji Uemura Masahiro Yao Yoshinobu Kubota |
author_sort | Takashi Kawahara |
collection | DOAJ |
description | The case was a 40-year-old female. She visited a local doctor with a chief complaint of right side abdominal pain. A right kidney tumor measuring 10 cm in diameter was observed in an abdominal Computed Tomography (CT) scan. Based on the CT image, the possibility of angiomiolipoma (AML) could not be ruled out, but a high maximum standardized uptake value (SUVmax) of 7.8 was observed in a Positron Emission Tomography CT (PET-CT) scan and there was a possibility of malignancy. We therefore performed a transperitoneal right radial nephrectomy. Although adhesion of the tumor to the duodenum and the inferior vena cava was observed, it was possible to perform an excision. The tumor accounted for a large proportion of the excised kidney; the surrounding areas had taken on a cyst-like structure, and the interior comprised grayish brittle tissue exhibiting solid growth. Histologically, gland-like and cyst-like structures composed of cylindrical cuboidal cells and mainly characterized by the solid growth of short fusiform-shaped and oval-shaped basophilic cells were observed, and we believed it was a synovial sarcoma. There were no malignant findings in the adrenal gland. There have been approximately 30 reported cases around the world of synovial sarcoma that developed in the kidney, and we herein report this case with bibliographic considerations. |
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format | Article |
id | doaj.art-21f46188447f4ea48059f696c27dd6e3 |
institution | Directory Open Access Journal |
issn | 1662-6575 |
language | English |
last_indexed | 2024-12-12T01:51:10Z |
publishDate | 2009-10-01 |
publisher | Karger Publishers |
record_format | Article |
series | Case Reports in Oncology |
spelling | doaj.art-21f46188447f4ea48059f696c27dd6e32022-12-22T00:42:29ZengKarger PublishersCase Reports in Oncology1662-65752009-10-012318919310.1159/000245926245926Primary Synovial Sarcoma of the KidneyTakashi KawaharaZenkichi SekiguchiKazuhide MakiyamaTakashi NakayamaYoji NagashimaKaoru KitaKazuhiro NamuraHiroki ItouFutoshi SanoNarihiko HayashiNoboru NakaigawaTakehiko OgawaHiroji UemuraMasahiro YaoYoshinobu KubotaThe case was a 40-year-old female. She visited a local doctor with a chief complaint of right side abdominal pain. A right kidney tumor measuring 10 cm in diameter was observed in an abdominal Computed Tomography (CT) scan. Based on the CT image, the possibility of angiomiolipoma (AML) could not be ruled out, but a high maximum standardized uptake value (SUVmax) of 7.8 was observed in a Positron Emission Tomography CT (PET-CT) scan and there was a possibility of malignancy. We therefore performed a transperitoneal right radial nephrectomy. Although adhesion of the tumor to the duodenum and the inferior vena cava was observed, it was possible to perform an excision. The tumor accounted for a large proportion of the excised kidney; the surrounding areas had taken on a cyst-like structure, and the interior comprised grayish brittle tissue exhibiting solid growth. Histologically, gland-like and cyst-like structures composed of cylindrical cuboidal cells and mainly characterized by the solid growth of short fusiform-shaped and oval-shaped basophilic cells were observed, and we believed it was a synovial sarcoma. There were no malignant findings in the adrenal gland. There have been approximately 30 reported cases around the world of synovial sarcoma that developed in the kidney, and we herein report this case with bibliographic considerations.http://www.karger.com/Article/FullText/245926Synovial sarcomaRenal tumorRenal massPET-CTSYT-SSX |
spellingShingle | Takashi Kawahara Zenkichi Sekiguchi Kazuhide Makiyama Takashi Nakayama Yoji Nagashima Kaoru Kita Kazuhiro Namura Hiroki Itou Futoshi Sano Narihiko Hayashi Noboru Nakaigawa Takehiko Ogawa Hiroji Uemura Masahiro Yao Yoshinobu Kubota Primary Synovial Sarcoma of the Kidney Case Reports in Oncology Synovial sarcoma Renal tumor Renal mass PET-CT SYT-SSX |
title | Primary Synovial Sarcoma of the Kidney |
title_full | Primary Synovial Sarcoma of the Kidney |
title_fullStr | Primary Synovial Sarcoma of the Kidney |
title_full_unstemmed | Primary Synovial Sarcoma of the Kidney |
title_short | Primary Synovial Sarcoma of the Kidney |
title_sort | primary synovial sarcoma of the kidney |
topic | Synovial sarcoma Renal tumor Renal mass PET-CT SYT-SSX |
url | http://www.karger.com/Article/FullText/245926 |
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