Cellular metanephric stromal tumor in a postmenopausal woman: a case report with review of the literature.

Abstract:

:Metanephric stromal tumor (MST) of the kidney is a rare pediatric neoplasm which has rarely been reported in adults. The authors present a case of MST, cellular type, an unreported variant, in a 56-year-old postmenopausal woman. The 9.0-cm tumor was solid, unencapsulated, and well circumscribed, with a firm homogeneous cut surface. The tumor was purely stromal with dense spindle-cell proliferations displaying prominent schwannoma-like architecture, intratumoral angiodysplasia, and entrapped native renal tubules with "onion-skin" tumor collarettes. The tumor stroma expressed CD34, estrogen, and progesterone and did not express desmin, smooth muscle actin, S-100, or TLE-1. Considering the characteristic morphology and immunophenotype, a diagnosis of "metanephric stromal tumor, cellular type," was made. This is an exceptionally rare disease manifestation in an adult patient and the first description of MST with such high stromal cellularity, making this case unique in both clinical and pathological presentation.

journal_name

Int J Surg Pathol

authors

Chaudhri AA,Lee L,Das K

doi

10.1177/1066896912453851

subject

Has Abstract

pub_date

2013-04-01 00:00:00

pages

153-60

issue

2

eissn

1066-8969

issn

1940-2465

pii

1066896912453851

journal_volume

21

pub_type

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