| Literature DB >> 27631338 |
Maria Pané Foix1,2, Ana Dunatov3, Petr Martinek4, Enric Condom Mundó1,2, Saul Suster5, Maris Sperga6, Jose I Lopez7, Monika Ulamec8, Stela Bulimbasic9, Delia Perez Montiel10, Reza Alaghehbandan11, Kvetoslava Peckova4, Krystina Pivovarcikova4, Daum Ondrej4, Pavla Rotterova4, Faruk Skenderi12, Kristyna Prochazkova13, Martin Dusek4, Milan Hora13, Michal Michal4, Ondrej Hes14,15.
Abstract
Chromophobe renal cell carcinoma (ChRCC) is typically composed of large leaf-like cells and smaller eosinophilic cells arranged in a solid-alveolar pattern. Eosinophilic, adenomatoid/pigmented, or neuroendocrine variants have also been described. We collected 10 cases of ChRCC with a distinct multicystic pattern out of 733 ChRCCs from our registry, and subsequently analyzed these by morphology, immunohistochemistry, and array comparative genomic hybridization. Of the 10 patients, 6 were males with an age range of 50-89 years (mean 68, median 69). Tumor size ranged between 1.2 and 20 cm (mean 5.32, median 3). Clinical follow-up was available for seven patients, ranging 1-19 years (mean 7.2, median 2.5). No aggressive behavior was documented. We observed two growth patterns, which were similar in all tumors: (1) variable-sized cysts, resembling multilocular cystic neoplasm of low malignant potential and (2) compressed cystic and tubular pattern with slit-like spaces. Raisinoid nuclei were consistently present while necrosis was absent in all cases. Half of the cases showed eosinophilic/oncocytic cytology, deposits of pigment (lipochrome) and microcalcifications. The other half was composed of pale or mixed cell populations. Immunostains for epithelial membrane antigen (EMA), CK7, OSCAR, CD117, parvalbumin, MIA, and Pax 8 were positive in all tumors while negative for vimentin, TFE3, CANH 9, HMB45, cathepsin K, and AMACR. Ki67 immunostain was positive in up to 1 % of neoplastic cells. Molecular genetic examination revealed multiple chromosomal losses in two fifths analyzable tumors, while three cases showed no chromosomal numerical aberrations. ChRCC are rarely arranged in a prominent multicystic pattern, which is probably an extreme form of the microcystic adenomatoid pigmented variant of ChRCC. The spectrum of tumors entering the differential diagnosis of ChRCC is quite different from that of conventional ChRCC. The immunophenotype of ChRCC is identical with that of conventional ChRCC. Chromosomal numerical aberration pattern was variable; no chromosomal numerical aberrations were found in three cases. All the cases in this series have shown an indolent and non-aggressive behavior.Entities:
Keywords: ArrayCGH; Chromophobe renal cell carcinoma; Immunohistochemistry; Kidney; Multicystic
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Year: 2016 PMID: 27631338 DOI: 10.1007/s00428-016-2022-x
Source DB: PubMed Journal: Virchows Arch ISSN: 0945-6317 Impact factor: 4.064