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. Author manuscript; available in PMC: 2015 Mar 7.
Published in final edited form as: Arch Pathol Lab Med. 2014 Nov;138(11):1531–1541. doi: 10.5858/arpa.2013-0653-RA

Figure 3.

Figure 3

A, Acquired cystic kidney disease (ACKD)–associated renal cell carcinoma (RCC) with intratumoral oxalate crystals (arrows). B, Atypical cysts in end-stage kidney disease with lining the same as ACKD-associated RCC, yet not forming solid mass. C, High-grade clear cell RCC (not shown) with rhabdoid (long arrows) and sarcomatoid (short arrows) differentiation. D, Microfollicular and macrofollicular architecture of follicular thyroid-like carcinoma with dense red and light pink secretions, correspondingly. E, Although cytologically this low-grade unclassified renal cell neoplasm is suggestive of oncocytoma, its dense growth pattern is not seen in the latter. F, Epithelioid angiomyolipoma composed of large bizarre cells with eosinophilic cytoplasm and smaller cells with pale cytoplasm and uniform small nucleoli (hematoxylin-eosin, original magnifications ×200 [A, B, and D], ×600 [C and E], and ×400 [F]).