Literature DB >> 10765150

Splenic lymphoma presenting as warm autoimmune hemolytic anemia associated with pure red cell aplasia.

A Zeidman1, Z Fradin, Y Barac, D Bendayan, M Mittelman, J Orlin.   

Abstract

BACKGROUND AND
OBJECTIVE: Warm autoimmune hemolytic anemia (AIHA) is a condition in which peripheral red blood cell (RBC) destruction is induced by the presence of an autoantibody. Pure red cell aplasia (PRCA) represents an isolated process of decreased erythropoiesis. The combination of both is quite rare, with a very poor prognosis. We describe a patient with isolated splenic lymphoma whose presentation was a combination of AIHA and PRCA. The patient was resistant to all treatment.
MATERIALS AND METHODS: Erythroid colony assays were performed, in order to compare the effect of the patient's serum on colonies with that of a normal control.
RESULTS: The patient's serum significantly suppressed normal erythroid colony growth. A red cell eluate revealed the presence of a warm autoantibody.
CONCLUSIONS: The patient's serum contained warm autoantibody responsible for peripheral RBC destruction and a humoral factor, perhaps the warm autoantibody, which suppressed bone marrow erythropoiesis. Establishing an early diagnosis, and treatment of the underlying disease might result in a better prognosis.

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Year:  2000        PMID: 10765150     DOI: 10.1159/000031163

Source DB:  PubMed          Journal:  Vox Sang        ISSN: 0042-9007            Impact factor:   2.144


  5 in total

1.  Autoimmune haemolytic anaemia associated with mantle cell lymphoma.

Authors:  Heather E Eve; Simon A J Rule
Journal:  Int J Hematol       Date:  2010-03       Impact factor: 2.490

2.  The co-existence of pure red cell aplasia and autoimmune haemolytic anaemia in a child with malignant lymphoma.

Authors:  Suhair Abbas Ahmed; Rosline Hassan
Journal:  Malays J Med Sci       Date:  2005-07

Review 3.  A case of recurrent autoimmune hemolytic anemia during remission associated with acute pure red cell aplasia and hemophagocytic syndrome due to human parvovirus B19 infection successfully treated by steroid pulse therapy with a review of the literature.

Authors:  Yasunobu Sekiguchi; Asami Shimada; Hidenori Imai; Mutsumi Wakabayashi; Keiji Sugimoto; Noriko Nakamura; Tomohiro Sawada; Norio Komatsu; Masaaki Noguchi
Journal:  Int J Clin Exp Pathol       Date:  2014-04-15

4.  Persistent anemia in a patient with diffuse large B cell lymphoma: pure red cell aplasia associated with latent Epstein-Barr virus infection in bone marrow.

Authors:  Hwa Jung Sung; Seok Jin Kim; Ji Hye Lee; Goeun Lee; Kyung A Lee; Chul Won Choi; Byung Soo Kim; Jun Suk Kim
Journal:  J Korean Med Sci       Date:  2007-09       Impact factor: 2.153

5.  Pure red cell aplasia as first manifestation of splenic marginal zone lymphoma-successful treatment with rituximab: a case report.

Authors:  Athanasios Anastasiadis; Dimitrios Margaritis; Ioannis Kotsianidis; Emmanouil Spanoudakis; Anna Christoforidou; Ioannis Kostopoulos; Constantinos Tsatalas
Journal:  Cases J       Date:  2009-08-18
  5 in total

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