Premium
Acquired pure red cell aplasia associated with malignant lymphomas: A nationwide cohort study in Japan for the PRCA Collaborative Study Group
Author(s) -
Hirokawa Makoto,
Sawada Kenichi,
Fujishima Naohito,
Kawano Fumio,
Kimura Akiro,
Watanabe Takashi,
Arai Ayako,
Matsui Toshimitsu,
Nakao Shinji,
Urabe Akio,
Omine Mitsuhiro,
Ozawa Keiya
Publication year - 2009
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.21354
Subject(s) - medicine , lymphoma , pure red cell aplasia , anemia , chemotherapy , cohort , oncology , gastroenterology
Pure red cell aplasia (PRCA) has been reported in association with lymphoma as one of the autoimmune diseases seen during the course of lymphoid malignancies. However, the relation of PRCA with the underlying lymphomas remains unclear. The aim of this study was to clarify the histologic subtypes of lymphomas, the chronological sequence of anemia and lymphoma, and the response to treatment. We conducted a nationwide survey in Japan. From a cohort of 185 PRCA patients, 8 patients with lymphoma were evaluated. Histologic subtypes varied and the lymphoma was of the B‐cell type in four cases and of the T‐cell type in four. Four patients simultaneously developed PRCA and lymphoma. Three patients developed PRCA following lymphoma, two of whom developed anemia during remission of lymphoma. PRCA preceded lymphoma in one patient. Effective chemotherapy was associated with remission of anemia in concurrent lymphoma and PRCA. Overall, anemia responded to chemotherapy and/or immunosuppressive therapy in seven patients. In four responding patients, PRCA remained in durable remission without maintenance immunosuppressive therapy, which is different from a recurrent feature of idiopathic PRCA. We suggest that the mechanism of lymphoma‐associated PRCA is heterogeneous and that durable maintenance‐free remission of anemia can be obtained in some patients. Am. J. Hematol., 2009. © 2008 Wiley‐Liss, Inc.