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儿童畸胎样肾母细胞瘤:1例罕见病例报告

Teratoid Wilms' tumor in a child: A report of a rare case.

作者信息

Sinha Anuradha, Phukan Jyoti Prakash, Bandyopadhyay Gautam, Mukherjee Sumana

机构信息

Department of Pathology, Bankura Sammilani Medical College, Bankura, India.

出版信息

Int J Appl Basic Med Res. 2013 Jan;3(1):72-4. doi: 10.4103/2229-516X.112248.

DOI:10.4103/2229-516X.112248
PMID:23776845
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3678687/
Abstract

Teratoid Wilms' tumor is an unusual variant of nephroblastoma in which heterologous tissue predominates. We report a case of teratoid Wilms' tumor in a 2-year-old male. Right sided abdominal mass was the presenting complaint. Ultrasonography of the abdomen showed a mass in the right kidney. Histopathological examination revealed blastemal, epithelial, and mesenchymal components along with areas presenting heterologous elements. More than 75% predominance of squamous differentiation with the keratin pearl formation was observed. The patient underwent nephrectomy and was followed post-operatively for 1 year and was normal.

摘要

畸胎样肾母细胞瘤是肾母细胞瘤的一种罕见变异型,其中异源性组织占主导。我们报告一例2岁男性的畸胎样肾母细胞瘤。主要症状为右侧腹部肿块。腹部超声检查显示右肾有一肿块。组织病理学检查发现有胚芽、上皮和间叶成分,以及存在异源性成分的区域。观察到鳞状分化占比超过75%,伴有角化珠形成。患者接受了肾切除术,术后随访1年,情况正常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2898/3678687/15a019ef88c9/IJABMR-3-72-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2898/3678687/35b560637660/IJABMR-3-72-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2898/3678687/836529fabae9/IJABMR-3-72-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2898/3678687/15a019ef88c9/IJABMR-3-72-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2898/3678687/35b560637660/IJABMR-3-72-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2898/3678687/836529fabae9/IJABMR-3-72-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2898/3678687/15a019ef88c9/IJABMR-3-72-g003.jpg

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本文引用的文献

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Teratoid Wilms' tumor: case report of a rare variant that can mimic aggressive biology during chemotherapy.畸胎瘤样 Wilms 瘤:一例罕见变异型病例报告,其在化疗期间可模拟侵袭性生物学行为。
J Pediatr Surg. 2011 Dec;46(12):e1-6. doi: 10.1016/j.jpedsurg.2011.09.049.
2
Teratoid Wilms' tumor - A rare renal tumor.畸胎样肾母细胞瘤——一种罕见的肾肿瘤。
Urol Ann. 2011 Sep;3(3):155-7. doi: 10.4103/0974-7796.84959.
3
Extrarenal teratoid Wilms' tumor: two cases in unusual locations, one associated with elevated serum AFP.肾外胚层组织来源的畸胎瘤性肾母细胞瘤:两例罕见部位发病病例,其中一例伴有血清 AFP 升高。
畸胎样肾母细胞瘤与经典型肾母细胞瘤:一项为期10年的单中心回顾性研究及文献综述
Front Surg. 2022 Feb 2;8:781060. doi: 10.3389/fsurg.2021.781060. eCollection 2021.
4
Long non-coding RNA HOXA11-AS upregulates Cyclin D2 to inhibit apoptosis and promote cell cycle progression in nephroblastoma by recruiting forkhead box P2.长链非编码RNA HOXA11-AS通过招募叉头框蛋白P2上调细胞周期蛋白D2,以抑制肾母细胞瘤细胞凋亡并促进细胞周期进程。
Am J Cancer Res. 2020 Jan 1;10(1):284-298. eCollection 2020.
5
Teratoid Wilms' tumor of kidney with neural tissue predominant: Case report with review of literature.以神经组织为主的肾畸胎瘤样威尔姆斯瘤:病例报告并文献复习
J Family Med Prim Care. 2019 Oct 31;8(10):3447-3449. doi: 10.4103/jfmpc.jfmpc_558_19. eCollection 2019 Oct.
6
Extrarenal teratoma with nephroblastoma in the retroperitoneum: Case report and literature review.腹膜后肾外畸胎瘤合并肾母细胞瘤:病例报告及文献复习
Medicine (Baltimore). 2017 Nov;96(46):e8670. doi: 10.1097/MD.0000000000008670.
Pathol Int. 2010 Jan;60(1):35-41. doi: 10.1111/j.1440-1827.2009.02468.x.
4
Stroma-predominant Wilms tumor with teratoid features: report of a rare case and review of the literature.具有类癌特征的基质为主型肾母细胞瘤:1例罕见病例报告并文献复习
Pediatr Surg Int. 2009 Mar;25(3):293-5. doi: 10.1007/s00383-009-2333-y. Epub 2009 Jan 29.
5
Adult teratoid Wilms' tumor with prominent neuroepithelial differentiation.具有显著神经上皮分化的成人畸胎样肾母细胞瘤。
Pathol Int. 2009 Jan;59(1):44-8. doi: 10.1111/j.1440-1827.2008.02323.x.
6
Teratoid Wilms' tumor, an important variant of nephroblastoma.畸胎样肾母细胞瘤,肾母细胞瘤的一种重要变体。
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