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
› Institutsangaben
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.



Publikationsverlauf

Eingereicht: 31. März 2018

Angenommen: 17. Mai 2018

Artikel online veröffentlicht:
19. Februar 2020

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