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Mixed epithelial and stromal tumor of the kidney in a 12‐year‐old girl
Author(s) -
Hara Noboru,
Kawaguchi Makoto,
Murayama Shinichirou,
Maruyama Ryo,
Tanikawa Toshiki,
Takahashi Kota
Publication year - 2005
Publication title -
pathology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
eISSN - 1440-1827
pISSN - 1320-5463
DOI - 10.1111/j.1440-1827.2005.01888.x
Subject(s) - girl , pathology , stromal cell , kidney , stromal tumor , medicine , biology , genetics
Mixed epithelial and stromal tumor of the kidney (MESTK) is a rare kidney neoplasm that almost exclusively occurs in perimenopausal women, and long‐term estrogen replacement is relevant to its pathogenesis. Herein is described an atypical case of MESTK uncovered in a 12‐year‐old premenarcheal girl without a history of prior estrogen use. On surgical specimen it was found that the well‐circumscribed tumor measuring 14 cm arose from the lower pole of the right kidney, showing solid and fibrous‐cystic areas. Microscopically, it was composed both of epithelial structures similar to renal tubules and stroma comprising non‐specific spindle cells. Some intratumoral tubules showed affinities to distal‐nephron‐specific lectins, and those immunoreactive for proximal‐tubule‐specific CD15 were also present. In addition, primitive ductal structures were reactive both for CD15 and lectins, but immature epithelial elements typical of nephroblastoma were absent. Spindle cells were positive for actin, desmin and vimentin, and expressed progesterone and estrogen receptors. The tumor was comparable with MESTK, although some epithelia were associated with the immunophenotype of proximal tubules. The patient was free of disease postoperatively for 40 months. In the present case, remnants of the primitive periductal mesenchyme might be promoted to neoplastic cells by a sex‐steroid surge during puberty.