Dobroński P, Czaplicki M, Koźmińska E, Pykało R
Department of Urology, Warsaw School of Medicine, Poland.
Int Urol Nephrol. 1999;31(5):601-9. doi: 10.1023/a:1007148219308.
We present clinical and radiological findings in a case of collecting (Bellini) duct carcinoma (CDC). This is a rare and aggressive kidney cancer originating from the distal renal tubule. The patient underwent radical nephrectomy and the pathological report showed trabeculopapillary, partially solid adenocarcinoma infiltrating the renal capsule and sinus. Immunohistochemical, as well as mucinocarminic and PAS staining studies are necessary for diagnosis of CDC. Surprisingly, one year follow-up studies were negative for recurrent disease. Chromosomal findings are usually different from most often diagnosed clear cell renal cell cancers. Findings from the literature are briefly discussed.
我们展示了一例集合管(贝氏管)癌(CDC)的临床和影像学表现。这是一种罕见且侵袭性强的肾癌,起源于远端肾小管。患者接受了根治性肾切除术,病理报告显示为小梁乳头状、部分实性腺癌,侵犯肾包膜和肾窦。免疫组织化学以及黏液卡红和PAS染色研究对于CDC的诊断是必要的。令人惊讶的是,一年的随访研究未发现复发性疾病。染色体表现通常与最常诊断的透明细胞肾细胞癌不同。文中简要讨论了文献中的研究结果。