| Literature DB >> 28038707 |
Kvetoslava Peckova1, Petr Martinek1, Kristyna Pivovarcikova1, Tomas Vanecek1, Reza Alaghehbandan2, Kristyna Prochazkova3, Delia Perez Montiel4, Milan Hora3, Faruk Skenderi5, Monika Ulamec6, Pavla Rotterova7, Ondrej Daum1, Jiri Ferda8, Whitney Davidson9, Ondrej Ondic1, Magdalena Dubova1, Michal Michal1, Ondrej Hes10.
Abstract
Conflicting data have been published on the prognostic significance of tumor necrosis in papillary renal cell carcinoma (PRCC). Although the presence of necrosis is generally considered an adverse prognostic feature in PRCC, we report a cohort of 10 morphologically distinct cystic and extensively necrotic PRCC with favorable biological behavior. Ten cases of type 1 PRCC with a uniform morphologic pattern were selected from the 19 500 renal tumors, of which 1311 were PRCCs in our registry. We focused on precise morphologic diagnosis supported by immunohistochemical and molecular-genetic analysis. Patients included 8 men and 2 women with an age range of 32-85 years (mean, 62.6 years). Tumor size ranged from 6 to 14 cm (mean, 9.4 cm). Follow-up data were available in 7 patients, ranging from 0.5 to 14 years (mean, 4 years). All tumors were spherical, cystic, and circumscribed by a thick fibrous capsule, filled with hemorrhagic/necrotic contents. Limited viable neoplastic tissue was present only as a thin rim in the inner surface of the cyst wall, consistent with type 1 PRCC. All cases were positive for AMACR, OSCAR, CAM 5.2, HIF-2, and vimentin. Chromosome 7 and 17 polysomy was found in 5 of 9 analyzable cases, 2 cases demonstrated chromosome 7 and 17 disomy, and 1 case showed only chromosome 17 polysomy. Loss of chromosome Y was found in 5 cases, including 1 case with disomic chromosomes 7 and 17. No VHL gene abnormalities were found. Papillary renal cell carcinoma type 1 can present as a large hemorrhagic/necrotic unicystic lesion with a thick fibroleiomyomatous capsule. Most cases showed a chromosomal numerical aberration pattern characteristic of PRCC. All tumors followed a nonaggressive clinical course. Large liquefactive necrosis should not necessarily be considered an adverse prognostic feature, particularly in a subset of type 1 PRCC with unilocular cysts filled with necrotic/hemorrhagic material.Entities:
Keywords: Cystic; Kidney; Molecular genetics; Necrosis; Necrotics; Papillary renal cell carcinoma
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Year: 2016 PMID: 28038707 DOI: 10.1016/j.anndiagpath.2016.10.007
Source DB: PubMed Journal: Ann Diagn Pathol ISSN: 1092-9134 Impact factor: 2.090