Pigmented microcystic chromophobe renal cell carcinoma: a clinicopathologic analysis of five cases
10.3760/cma.j.issn.0529-5807.2018.12.006
- VernacularTitle: 色素微囊性嫌色细胞肾细胞癌五例临床病理学特征
- Author:
Ming ZHAO
1
;
Yubin WANG
;
Qi ZHANG
;
Li JIN
;
Zeran YANG
;
Xin ZHANG
;
Guoqing RU
;
Dahong ZHANG
;
Xianglei HE
Author Information
1. Department of Pathology, Zhejiang Provincial People′s Hospital, People′s Hospital of Hangzhou Medical College, Hangzhou 310014, China
- Publication Type:Journal Article
- Keywords:
Carcinoma, renal cell;
Carcinoma, papillary;
Diagnosis, differential
- From:
Chinese Journal of Pathology
2018;47(12):926-930
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To investigate the clinicopathologic features, diagnostic and differential diagnostic aspects of pigmented microcystic chromophobe renal cell carcinoma (ChRCC).
Methods:Five cases of pigmented microcystic ChRCC were collected at Zhejiang Provincial People′s Hospital from January 2013 to January 2018. The clinical features, gross and histological appearances, immunohistochemistry and prognosis were analyzed and the relevant literature was reviewed.
Results:There were 3 men and 2 women with age range of 45 years to 72 years (mean 57 years). All tumors were incidentally identified by imaging examinations. Grossly, the tumors were well-demarcated and showed diameters ranging from 1.8 cm to 4.0 cm(mean 2.9 cm). On cross section, the tumors were brown to gray tan with solid cut-surface mixed with multiple cysts of variable sizes. Hemorrhage was common, central scar was not seen. Microscopically, the tumors were composed predominantly of irregular and variable-sized microcystic or tubulocystic patterns, with extensive cribriform structures formation and focal adenomatous rearrangements seen in one case each, and focal pseudo-papillary structures (lacking true fibro-vascular cores) seen in two cases. Microscopic calcifications and psammoma bodies were present in all tumors. Four tumors composed mostly of eosinophilic cells whereas 1 predominated in plant-like cells. Brown pigmentations, either intracytoplasmic or extracytoplasmic, were noted in all five cases. The tumor cells had irregular, low-grade nuclei (Paner grade: 1) frequently with binucleation and perinuclar halos. Tumor necrosis or sarcomatous transformation was not seen. By immunohistochemistry, the tumor cells expressed CK, EMA, and E-cadherin diffusely and strongly in five cases; and CK7 and CD117 diffusely in four cases. They were negative for vimentin, CD10, CA9, AMACR/P504s, TFE3, HMB45, Melan A, S-100 protein, synaptophysin and chromogranin. Partial nephrectomies were performed for all five patients; there was no tumor recurrences or metastases at a follow-up of 2 to 55 months (mean, 17 months).
Conclusions:Pigmented microcystic ChRCC is a rare histological variant of ChRCC with relatively indolent behavior, and shows morphologic heterogeneity which can elicit a wide range of differential diagnoses. Careful attentions to search for typical features of classic ChRCC with the use of immunohistochemistry can help to distinguish this tumor from its many mimickers.
