Pure red cell aplasia caused by ribavirin and interferon treatment

被引:3
|
作者
Skabelund A.J. [1 ]
Hauser T.R. [1 ]
Goist K.J. [1 ]
机构
[1] 88th Medical Group, Department of Internal Medicine, Wright-Patterson Medical Center, Wright-Patterson Air Force Base, OH 45433
关键词
Hepatitis C; Interferon; Pure red cell aplasia; Ribavirin;
D O I
10.1007/s12328-011-0235-8
中图分类号
学科分类号
摘要
Anemia is a common complication of hepatitis C (HCV), and antiviral treatment can further increase this risk. We present the case of a 59-year-old man with HCV treated with ribavirin and pegylated interferon alpha (INF-α) who presented with severe anemia. Two months after initiating treatment his hemoglobin dropped from 14.2 to 5.0 g/dL. There was no evidence of bleeding or hemolysis, and a bone marrow biopsy revealed pure red cell aplasia (PRCA). Evaluations for acute cytomegalovirus and parvovirus B19 were negative. There was no evidence of malignancy or thymoma. The INF-α and ribavirin treatment were determined to have caused the PRCA, and withdrawal of the medications led to PRCA remission. INF-α and ribavirin have become the standard treatment for HCV. While these medications offer a potential cure, they are often poorly tolerated due to frequent side effects including anemia. Patients who are receiving treatment with ribavirin and INF-α warrant close monitoring for development of anemia, and PRCA should be considered in all patients in whom reticulocytopenic anemia develops. © 2011 Springer.
引用
收藏
页码:313 / 317
页数:4
相关论文
共 50 条
  • [1] Pure red cell aplasia caused by pegylated interferon-α-2a plus ribavirin in the treatment of chronic hepatitis C
    Chang, Cheng-Shyong
    Yan, Sheng-Lei
    Lin, Hsuan-Yu
    Yu, Fu-Lien
    Tsai, Chien-Yu
    WORLD JOURNAL OF GASTROENTEROLOGY, 2011, 17 (16) : 2155 - 2158
  • [2] Pure red cell aplasia caused by pegylated interferon-α-2a plus ribavirin in the treatment of chronic hepatitis C
    Cheng-Shyong Chang
    Hsuan-Yu Lin
    Fu-Lien Yu
    Chien-Yu Tsai
    Sheng-Lei Yan
    World Journal of Gastroenterology, 2011, 17 (16) : 2155 - 2158
  • [3] Treatment of pure red cell aplasia
    Crabol, Y.
    Mouthon, L.
    REVUE DE MEDECINE INTERNE, 2008, 29 : 36 - 43
  • [4] Pure red cell aplasia secondary to treatment with erythropoietin
    Locatelli, F
    Del Vecchio, L
    JOURNAL OF NEPHROLOGY, 2003, 16 (04) : 461 - 466
  • [5] Pure red cell aplasia: Diagnosis, classification and treatment
    Lobbes, Herve
    REVUE DE MEDECINE INTERNE, 2023, 44 (01): : 19 - 26
  • [6] Pure red cell aplasia
    Fisch, P
    Handgretinger, R
    Schaefer, HE
    BRITISH JOURNAL OF HAEMATOLOGY, 2000, 111 (04) : 1010 - 1022
  • [7] Corticosteroid Treatment of Pure Red Cell Aplasia in a Patient with Hepatitis A
    Yoon, Young Kyung
    Park, Dae Won
    Sohn, Jang Wook
    Kim, Min Ja
    Kim, Insun
    Myung Hyun Nam
    ACTA HAEMATOLOGICA, 2012, 128 (01) : 60 - 63
  • [8] Acquired pure red cell aplasia: updated review of treatment
    Sawada, Kenichi
    Fujishima, Naohito
    Hirokawa, Makoto
    BRITISH JOURNAL OF HAEMATOLOGY, 2008, 142 (04) : 505 - 514
  • [9] Cyclosporin a for the treatment of pure red cell aplasia associated with myelodysplasia
    Grigg, AP
    O'Flaherty, E
    LEUKEMIA & LYMPHOMA, 2001, 42 (06) : 1339 - 1342
  • [10] Pure red cell aplasia and lupus
    Habib, GS
    Saliba, WR
    Froom, P
    SEMINARS IN ARTHRITIS AND RHEUMATISM, 2002, 31 (04) : 279 - 283