Diagnosing liposarcoma on (peri)‐renal mass biopsy: A clinicopathological study of 30 cases

Author:

Potterveld Susan K1ORCID,Mubeen Aysha2,Anderson William J3ORCID,Clay Michael R4,Bourgeau Melanie4,Charville Gregory W1ORCID,Sangoi Ankur R1

Affiliation:

1. Department of Pathology Stanford Medical Center Stanford CA USA

2. University of New Mexico Albuquerque NM USA

3. Brigham and Women's Hospital Boston MA USA

4. University of Colorado Aurora CO USA

Abstract

AimsClassification of renal neoplasms on small tissue biopsies is in increasing demand, and maintaining broad differential diagnostic considerations in this setting is necessary. When evaluating a renal or perirenal tumour biopsy with sarcomatoid morphology, together with sarcomatoid renal cell carcinoma and sarcomatoid urothelial carcinoma as top diagnostic considerations, it is vital to additionally consider the possibility of well‐differentiated and de‐differentiated liposarcoma.Methods and resultsThis study reports a series of 30 biopsy samples from sites in or around the kidney collected from four institutions in which the correct diagnosis was either well‐differentiated or de‐differentiated liposarcoma. The majority (26 of 30, 87%) of lesions were accurately diagnosed on biopsy sampling, all of which incorporated testing for MDM2 by immunohistochemistry (IHC), fluorescence in‐situ hybridisation (FISH) or a combination of the two as part of the diagnostic work‐up. Tumour expression of MDM2 by IHC without confirmatory FISH analysis was sometimes (30%) sufficient to reach a diagnosis, but demonstration of MDM2 amplification by FISH was ascertained in the majority (57%) of biopsy samples. A diagnosis of de‐differentiated liposarcoma was not definitively established until resection in four (13%) patients, as no MDM2 testing was performed on the corresponding pre‐operative biopsies.ConclusionsWhen a retroperitoneal tumour is not clinically suspected, histological consideration of a liposarcoma diagnosis may be overlooked. Implementation of ancillary immunohistochemical and cytogenetic testing can ultimately lead to a definitive diagnosis in this potentially misleading anatomical location.

Publisher

Wiley

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