Thanks for the follow-up with immunstain result. I have seen quite a few angiomyolipoma (AML) including some atypica ones, such as myoid rich, epithelioid, pigmented, cystic etc. Some can have significant cytologic atypia. But combinations of cytologic atypia + hypercelluarity + necrosis are rare. I still worry about sarcomatoid carcinoma. Immunostain with other markers including pan-cytokeratin, AE1/3, SMA are also necessary to confirm the diagnosis of a atypical angiomyolipoma. Also a symptomatic 3.0 cm AML will be pretty rare. Opinions from
曲直 ﹢指环王 ﹢pathdoc will certainly help. Thanks.