Challenges of Managing Multiple Myeloma Patients with Sickle Cell Disease: A Case Report and Review of Literature

被引:1
|
作者
Zerdan, Maroun Bou [1 ]
Diacovo, Maria Julia [2 ]
Chaulagain, Chakra P. [1 ]
机构
[1] Cleveland Clin Florida, Maroone Canc Ctr, Myeloma & Amyloidosis Program, Weston, FL 33331 USA
[2] Cleveland Clin Florida, Dept Pathol, Weston, FL USA
来源
关键词
Anemia; Sickle Cell; Multiple Myeloma; pomalidomide; CONGENITAL DYSERYTHROPOIETIC ANEMIA; EXTRAMEDULLARY HEMATOPOIETIC TUMOR; THALASSEMIA; LEUKEMIA; POMALIDOMIDE; DISORDERS; HEMOLYSIS;
D O I
10.12659/AJCR.933470
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Rare coexistence of disease or pathology Background: A congenital hemolytic anemia, sickle cell disease can present with various clinical findings. Sickle cell disease is typically a disease of younger people and multiple myeloma typically occurs in older individuals. Multiple myeloma is rare among patients with sickle cell disease. Both multiple myeloma and sickle cell disease can cause various types of organ damage by different mechanisms. Case Report: We report a case of a patient who was born with sickle cell disease and presented with multiple myeloma later in life. Although he responded to anti-myeloma therapy, he died of hepatic and renal failure from complications of both multiple myeloma and sickle cell disease. Conclusions: We discuss the complexity involved and present a review of the literature on managing multiple myeloma in relation to hepatic iron overload and end-stage renal disease in the setting of multiple myeloma and underlying sickle cell disease.
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页数:6
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