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Adult Pleomorphic Juxtaglomerular Cell Tumor.

作者信息

Soni Abha, Gordetsky Jennifer B

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL.

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL; Department of Urology, University of Alabama at Birmingham, Birmingham, AL.

出版信息

Urology. 2016 Jan;87:e5-7. doi: 10.1016/j.urology.2015.09.019. Epub 2015 Oct 3.

DOI:10.1016/j.urology.2015.09.019
PMID:26435458
Abstract

A 40-year-old male with chronic hypertension since his teens presented to the emergency department following a motor vehicle collision. Computed tomography scan demonstrated an incidental 1.8-cm renal mass. Partial nephrectomy revealed a vascular tumor with predominantly monomorphic epithelioid cells arranged in sheets and trabeculae with foci of nuclear pleomorphism. Tumor cells were positive for vimentin, CD34, and c-KIT. Juxtaglomerular cell tumor is a rare, benign neoplasm typically found in young adults. Pleomorphism is uncommon and, in combination with older age at diagnosis, can lead to an inaccurate malignant diagnosis. Immunohistochemistry and clinical history helps in correctly diagnosing this benign entity.

摘要

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引用本文的文献

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The Small Size and Superficial Location Suggest That Laparoscopic Partial Nephrectomy Is the First Choice for the Treatment of Juxtaglomerular Cell Tumors.体积小且位置表浅提示腹腔镜部分肾切除术是治疗肾小球旁细胞瘤的首选方法。
Front Endocrinol (Lausanne). 2021 Apr 30;12:646649. doi: 10.3389/fendo.2021.646649. eCollection 2021.