Literature DB >> 8136286

Pure red cell aplasia of pregnancy: a distinct clinical entity.

R I Baker1, A Manoharan, E de Luca, C G Begley.   

Abstract

We describe a 31-year-old patient with pure red cell aplasia of pregnancy, successfully managed with regular blood transfusions. In vitro studies showed specific inhibition of day 14 erythroid colonies (BFU-E) using serum and purified immunoglobulin G (IgG) obtained from the patient at diagnosis (before blood transfusion). The inhibition of BFU-E disappeared when haematological remission occurred 3 weeks after delivery and she remains clinically well with a normal haemoglobin 4 years later.

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Year:  1993        PMID: 8136286     DOI: 10.1111/j.1365-2141.1993.tb03359.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  4 in total

Review 1.  Anemia of Central Origin.

Authors:  Kazusa Ishii; Neal S Young
Journal:  Semin Hematol       Date:  2015-07-09       Impact factor: 3.851

2.  Recurrent severe anaemia: a rare presentation of parvovirus b19 infection.

Authors:  Santokh Singh; Gian Chand; Shiv Charan; Sahil Arora; Parampreet Singh
Journal:  J Clin Diagn Res       Date:  2014-04-15

3.  Reversible pure red cell aplasia of pregnancy: a therapeutic challenge.

Authors:  Sunita Aggarwal
Journal:  J Obstet Gynaecol India       Date:  2012-04-14

4.  Self-limiting pregnancy-associated pure red cell aplasia developing in two consecutive pregnancies: case report and literature review.

Authors:  Yoko Edahiro; Hajime Yasuda; Kiyoshi Ando; Norio Komatsu
Journal:  Int J Hematol       Date:  2019-12-09       Impact factor: 2.490

  4 in total

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