Secondary Immune Thrombocytopenic Purpura in Renal Cell Cancer: A Paraneoplastic Syndrome

被引:2
作者
Noor, Arish [1 ]
Rehan, Anam [1 ]
Desai, Aakash [2 ]
Iorgoveanu, Corina [2 ]
Lee, Jim C. [3 ]
机构
[1] Univ Connecitcut, Internal Med, Hartford, CT 06103 USA
[2] Univ Connecticut, Internal Med, Hlth Ctr, Hartford, CT USA
[3] Hartford Hosp, Pathol, Hartford, CT 06115 USA
关键词
paraneoplastic syndrome; immune thrombocytopenic purpura; renal cell cancer; AUTOIMMUNE HEMOLYTIC-ANEMIA; SOLID TUMORS; PATIENT;
D O I
10.7759/cureus.4398
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Secondary immune thrombocytopenic purpura (ITP) as a paraneoplastic syndrome has been reported in literature. It is commonly associated with chronic lymphocytic leukemia (CLL) and hodgkins lymphoma. Its association with solid malignancies, especially renal cell cancer is rare, with only a few documented case reports. Treatment usually consisted of targeting the underlying malignancy or utilization of steroid and intravenous immunoglobulin (IVIG) to improve thrombocytopenia. Here, we describe a case of a 75-year-old man with renal cell cancer (RCC), who presented with secondary thrombocytopenia treated with steroid and IVIG. It is important to keep RCC in differential diagnosis for causes for secondary ITP as this impacts treatment.
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页数:7
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