Korean J Hematol 2006; 41(3):
Published online September 30, 2006
https://doi.org/10.5045/kjh.2006.41.3.199
© The Korean Society of Hematology
김일영, 문지윤, 송무곤, 안용성, 김경엽, 최영진, 신호진, 정주섭, 조군제
부산대학교 의과대학 내과학교실
We experienced a 22-year old patient with a documented history of minimal change nephrotic syndrome (MCNS), and a diagnosis of acute lymphoblastic leukemia (ALL) was then made for this patient. The patient received standard daily steroid therapy for the treatment of nephrotic syndrome. Cyclosporin A was administered because there was no clinical improvement with steroid therapy. Six years after the diagnosis of nephrotic syndrome, the patient was diagnosed with ALL. After chemotherapy for ALL, the patient was in complete remission and he showed clinical improvement of nephrotic syndrome. The hematological malignancies associated with nephrotic syndrome are mainly lymphoma and chronic lymphocytic leukemia. ALL has rarely been described in combination with nephrotic syndrome. Although the exact mechanism for development of ALL after nephrotic syndrome is unknown, at least two possibilities exist. First, the incidence of leukemia may be increased after immunosuppressive therapy, which may include cyclosporin A. Second, the underlying defect in T-lymphocyte function could account for both nephrotic syndrome and ALL. The possible mechanisms for such a relationship are discussed here along with a review of the relevant literature.
Keywords Acute lymphoblastic leukemia, Nephrotic syndrome, Cyclosporin A
Korean J Hematol 2006; 41(3): 199-203
Published online September 30, 2006 https://doi.org/10.5045/kjh.2006.41.3.199
Copyright © The Korean Society of Hematology.
김일영, 문지윤, 송무곤, 안용성, 김경엽, 최영진, 신호진, 정주섭, 조군제
부산대학교 의과대학 내과학교실
Il Young Kim, Ji Yoon Moon, Moo Kon Song, Yong Sung Ahn, Kyung Yup Kim, Young Jin Choi, Ho Jin Shin, Joo Seop Chung, Goon Jae Cho
Department of Internal Medicine, Pusan National University College of Medicine, Busan, Korea
We experienced a 22-year old patient with a documented history of minimal change nephrotic syndrome (MCNS), and a diagnosis of acute lymphoblastic leukemia (ALL) was then made for this patient. The patient received standard daily steroid therapy for the treatment of nephrotic syndrome. Cyclosporin A was administered because there was no clinical improvement with steroid therapy. Six years after the diagnosis of nephrotic syndrome, the patient was diagnosed with ALL. After chemotherapy for ALL, the patient was in complete remission and he showed clinical improvement of nephrotic syndrome. The hematological malignancies associated with nephrotic syndrome are mainly lymphoma and chronic lymphocytic leukemia. ALL has rarely been described in combination with nephrotic syndrome. Although the exact mechanism for development of ALL after nephrotic syndrome is unknown, at least two possibilities exist. First, the incidence of leukemia may be increased after immunosuppressive therapy, which may include cyclosporin A. Second, the underlying defect in T-lymphocyte function could account for both nephrotic syndrome and ALL. The possible mechanisms for such a relationship are discussed here along with a review of the relevant literature.
Keywords: Acute lymphoblastic leukemia, Nephrotic syndrome, Cyclosporin A
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