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肾间变性肉瘤:病例报告及文献复习

Anaplastic sarcoma of the kidney: Case report and literature review.

作者信息

Chen Chien-Chin, Liao Kai-Sheng

机构信息

Department of Pathology, Ditmanson Medical Foundation, Chiayi Christian Hospital, Chiayi, Taiwan.

Department of Cosmetic Science, Chia Nan University of Pharmacy and Science, Tainan, Taiwan.

出版信息

Tzu Chi Med J. 2019 Apr-Jun;31(2):129-132. doi: 10.4103/tcmj.tcmj_194_18.

DOI:10.4103/tcmj.tcmj_194_18
PMID:31007495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6450149/
Abstract

We present a case of a 22-year-old female with gross hematuria for 1 month. A 9.5-cm tumor was found at her left kidney. On suspicion of a renal cancer, she received left nephrectomy. Histologically, it was a hypercellular tumor with undifferentiated anaplastic neoplastic cells in fascicular sheets intermixed with chondroid nodules. The differential diagnoses included anaplastic sarcoma of the kidney (ASK), anaplastic Wilms tumor, mesenchymal chondrosarcoma, sarcomatoid renal cell carcinoma, clear cell sarcoma of the kidney, rhabdoid tumor of the kidney, congenital mesoblastic nephroma, and synovial sarcoma. Based on the results of the work-up and literature review, ASK was diagnosed. The postoperative recovery was uneventful, and the patient began adjuvant chemotherapy (Ifosfamide [1800 mg/m] and Epirubicin [60 mg/m]) 5 weeks after the operation. Herein, we present this case to share the experience on an extremely rare entity.

摘要

我们报告一例22岁女性,肉眼血尿1个月。在其左肾发现一个9.5厘米的肿瘤。因怀疑为肾癌,她接受了左肾切除术。组织学检查显示,这是一个细胞增多的肿瘤,有未分化的间变肿瘤细胞呈束状排列,并夹杂软骨样结节。鉴别诊断包括肾间变性肉瘤(ASK)、间变性威尔姆斯瘤、间叶性软骨肉瘤、肉瘤样肾细胞癌、肾透明细胞肉瘤、肾横纹肌样瘤、先天性中胚层肾瘤和滑膜肉瘤。根据检查结果及文献复习,诊断为ASK。术后恢复顺利,患者在术后5周开始辅助化疗(异环磷酰胺[1800毫克/平方米]和表柔比星[60毫克/平方米])。在此,我们呈现此病例以分享关于这一极其罕见疾病的经验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c17e/6450149/6c4fe5755c9d/TCMJ-31-129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c17e/6450149/08449ae540a3/TCMJ-31-129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c17e/6450149/6c4fe5755c9d/TCMJ-31-129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c17e/6450149/08449ae540a3/TCMJ-31-129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c17e/6450149/6c4fe5755c9d/TCMJ-31-129-g002.jpg

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本文引用的文献

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Tumor progression in DICER1-mutated cystic nephroma-witnessing the genesis of anaplastic sarcoma of the kidney.DICER1突变型囊性肾瘤中的肿瘤进展——见证肾间变性肉瘤的发生
Hum Pathol. 2016 Jul;53:114-20. doi: 10.1016/j.humpath.2016.03.002. Epub 2016 Mar 29.
2
Anaplastic Sarcoma of the Kidney: A Rare Unique Renal Neoplasm.肾间变性肉瘤:一种罕见的独特肾脏肿瘤。
Int J Surg Pathol. 2016 Sep;24(6):556-61. doi: 10.1177/1066896916639373. Epub 2016 Mar 21.
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Diffuse and strong cyclin D1 immunoreactivity in clear cell sarcoma of the kidney.
Nat Rev Urol. 2025 Jan 29. doi: 10.1038/s41585-024-00993-6.
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Rare anaplastic sarcoma of the kidney: A case report.罕见的肾间变性肉瘤:一例报告。
World J Clin Cases. 2020 Apr 26;8(8):1495-1501. doi: 10.12998/wjcc.v8.i8.1495.
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Case Report: Partial nephrectomy in primary renal sarcoma presenting as Wunderlich syndrome; a rare tumour with rare presentation managed atypically.病例报告:表现为温德利希综合征的原发性肾肉瘤行部分肾切除术;一种罕见肿瘤的罕见表现,采用非典型治疗。
F1000Res. 2019 Apr 10;8:423. doi: 10.12688/f1000research.18698.1. eCollection 2019.
肾透明细胞肉瘤中弥漫且强烈的细胞周期蛋白D1免疫反应性。
Histopathology. 2015 Sep;67(3):306-12. doi: 10.1111/his.12641. Epub 2015 Mar 20.
4
Anaplastic sarcoma of the kidney: case report and literature review.肾间变性肉瘤:病例报告及文献综述
Pediatr Int. 2013 Oct;55(5):e129-32. doi: 10.1111/ped.12167.
5
Anaplastic sarcoma of the kidney with chromosomal abnormality: first report on cytogenetic findings.肾脏间变性横纹肌肉瘤伴染色体异常:细胞遗传学研究结果的首次报道。
Hum Pathol. 2010 Oct;41(10):1495-9. doi: 10.1016/j.humpath.2010.03.008. Epub 2010 Jul 24.
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Anaplastic sarcoma of the kidney.肾间变性肉瘤
ScientificWorldJournal. 2009 Feb 15;9:97-101. doi: 10.1100/tsw.2009.15.
7
Anaplastic sarcoma of the kidney: a clinicopathologic study of 20 cases of a new entity with polyphenotypic features.肾间变性肉瘤:20例具有多表型特征的新实体的临床病理研究
Am J Surg Pathol. 2007 Oct;31(10):1459-68. doi: 10.1097/PAS.0b013e31804d43a4.