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CC BY-NC-ND 4.0 · J Lab Physicians 2018; 10(03): 351-353
DOI: 10.4103/JLP.JLP_42_18
Case Report

Primitive neuroectodermal tumor of the kidney: A rare case report

Amrita Talwar
Department of Pathology, Dr. RML Hospital, PGIMER, New Delhi, India
,
Manjari Kishore
Department of Pathology, Dr. RML Hospital, PGIMER, New Delhi, India
,
Minakshi Bhardwaj
Department of Pathology, Dr. RML Hospital, PGIMER, New Delhi, India
,
Devender Singh Chauhan
Department of Pathology, Dr. RML Hospital, PGIMER, New Delhi, India
› Author Affiliations Financial support and sponsorship: Nil
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ABSTRACT

Renal primitive neuroectodermal tumor (PNET) is a rare primary renal neoplasm. Morphologically, it may mimic small blue round-cell tumor. Hence, histopathology in conjunction with immunohistochemistry plays a significant role in correctly diagnosing this malignancy. We report a case of PNET of kidney in a 30-year-old female with an extension to inferior vena cava, who succumbed following an aggressive course of illness.

Keywords

Histopathology - immunohistochemistry - primitive neuroectodermal tumor - renal - small-round-cell tumor


Publication History

Received: 31 March 2018

Accepted: 17 May 2018

Article published online:
19 February 2020

© 2018.

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