Maekawa Shigekatsu, Nagata Masayoshi, Watanabe Hiroshi, Nozaki Keina, Takahashi Atsuko, Minowada Shigeru, Homma Yukio
Department of Urology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Urology, National Center for Global Health and Medicine, Tokyo, Japan.
Int J Urol. 2015 Dec;22(12):1167-9. doi: 10.1111/iju.12944. Epub 2015 Sep 9.
Idiopathic thrombocytopenic purpura associated with renal cell carcinoma is relatively rare. We report the case of a 48-year-old woman with massive renal cell carcinoma, measuring approximately 20 × 14 × 14 cm, who presented with severe thrombocytopenia: platelet count, 2000 cells/μL. After confirming normal bone marrow, she received high-dose dexamethasone and intravenous gamma globulin, which raised the platelet count to normal levels. She then underwent left radical nephrectomy. The pathological examination showed chromophobe renal cell carcinoma. After the resection, the platelet count was maintained within the normal range without any treatment. The current case is the first report of chromophobe renal cell carcinoma causative of severe idiopathic thrombocytopenic purpura.
与肾细胞癌相关的特发性血小板减少性紫癜相对罕见。我们报告了一例48岁女性,患有巨大肾细胞癌,大小约为20×14×14cm,出现严重血小板减少:血小板计数为2000个/μL。在确认骨髓正常后,她接受了大剂量地塞米松和静脉注射丙种球蛋白治疗,血小板计数升至正常水平。随后她接受了左肾根治性切除术。病理检查显示为嫌色性肾细胞癌。切除术后,血小板计数在未进行任何治疗的情况下维持在正常范围内。本病例是关于嫌色性肾细胞癌导致严重特发性血小板减少性紫癜的首例报告。