| Literature DB >> 29024210 |
Yuzo Oyama1, Haruto Nishida1, Takahiro Kusaba1, Hiroko Kadowaki1, Motoki Arakane1, Tsutomu Daa1, Dai Watanabe2, Yasuyuki Akita2, Fuminori Sato2, Hiromitsu Mimata2, Shigeo Yokoyama1.
Abstract
We report a case of ALK-positive renal cell carcinoma coincident with Hodgkin lymphoma. The patient was a 19 year-old-girl without sickle cell trait. The right renal tumor was discovered concomitantly with Hodgkin lymphoma (HL). After chemotherapy for HL, right nephrectomy was performed. Microscopically, the tumor showed a solid and focally pseudo-papillary growth pattern studded with tubular structures. Most tumor cells were small bland eosinophilic cells, but rhabdoid cells, vacuolated cells, pleomorphic multinucleated giant cells were also admixed. The variety of growth patterns and cell features led us to speculate a possibility of ALK-positive renal cell carcinoma (ALK + RCC). ALK was immunohistochemically positive, and fluorescence in situ hybridization analysis detected a split signal of the ALK gene. We examined previously reported partner genes (STRN, TPM3, VCL and EML4) by RT-PCR, but fusion gene was not detected. RCC showing solid or cribriform growth patterns with vacuolated cells with intracytoplamic lumina, rhabdoid cells, and mucus production indicates the possibility of ALK + RCC.Entities:
Keywords: anaplastic lymphoma kinase (ALK); hodgkin lymphoma; kidney; renal cell carcinoma
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Year: 2017 PMID: 29024210 DOI: 10.1111/pin.12592
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534