Literature DB >> 19225748

[Autoimmune thrombocytopenia, neutropenia and hemolysis].

A Greinacher1, J Bux, A Salama.   

Abstract

Autoantibodies reduce the life span of platelets, granulocytes, and red blood cells. This may result in thrombocytopenia with bleeding, in neutropenia with infection, and in anemia, respectively. Immune-hemocytopenias can manifest as primary disease without another cause, or they are associated with other underlying morbidities such as autoimmune diseases, lymphoproliferative diseases, immune defects, or viral infections. Diagnosis is confirmed by laboratory tests showing autoantibodies against the respective blood cells. Indication for treatment is the clinical manifestation of symptoms: bleeding in autoimmune thrombocytopenia, infections in neutropenia, and symptomatic anemia, respectively. Especially in case of thrombocytopenia patients should not be treated because of abnormal laboratory values, only. To date steroids are the basic treatment in autoimmune thrombocytopenia and hemolytic anemia, while prophylactic antibiotics are the main treatment in autoimmune neutropenia. Growth factors like the new thrombopoietin receptor agnonists in autoimmune thrombocytopenia or G-CSF in autoimmune neutropenia, and anti-CD20 antibodies are new options for treatment.

Entities:  

Mesh:

Year:  2009        PMID: 19225748     DOI: 10.1007/s00108-008-2250-5

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN: 0020-9554            Impact factor:   0.743


  49 in total

1.  Morbidity and mortality in adults with idiopathic thrombocytopenic purpura.

Authors:  J E Portielje; R G Westendorp; H C Kluin-Nelemans; A Brand
Journal:  Blood       Date:  2001-05-01       Impact factor: 22.113

2.  Randomised trial of intravenous immunoglobulin G, intravenous anti-D, and oral prednisone in childhood acute immune thrombocytopenic purpura.

Authors:  V Blanchette; P Imbach; M Andrew; M Adams; J McMillan; E Wang; R Milner; K Ali; D Barnard; M Bernstein
Journal:  Lancet       Date:  1994-09-10       Impact factor: 79.321

Review 3.  Therapy of chronic idiopathic thrombocytopenic purpura in adults.

Authors:  P Berchtold; R McMillan
Journal:  Blood       Date:  1989-11-15       Impact factor: 22.113

Review 4.  Mixed-type autoimmune hemolytic anemia: differential diagnosis and a critical review of reported cases.

Authors:  Beate Mayer; Salih Yürek; Holger Kiesewetter; Abdulgabar Salama
Journal:  Transfusion       Date:  2008-06-28       Impact factor: 3.157

5.  Efficacy of prophylactic use of trimethoprim-sulfamethoxazole in autoimmune neutropenia in infancy.

Authors:  Masao Kobayashi; Takashi Sato; Hiroshi Kawaguchi; Kazuhiro Nakamura; Hirotaka Kihara; Asako Hiraoka; Misae Tanihiro; Kikuyo Taniguchi; Noboru Takata; Kazuhiro Ueda
Journal:  J Pediatr Hematol Oncol       Date:  2003-07       Impact factor: 1.289

6.  Massive platelet transfusion is a rapidly effective emergency treatment in patients with refractory autoimmune thrombocytopenia.

Authors:  Abdulgabar Salama; Holger Kiesewetter; Ulrich Kalus; Kamran Movassaghi; Oliver Meyer
Journal:  Thromb Haemost       Date:  2008-11       Impact factor: 5.249

7.  Clinical and therapeutic experience in 712 Israeli patients with idiopathic thrombocytopenic purpura. Israeli ITP Study Group.

Authors:  D Ben-Yehuda; S Gillis; A Eldor
Journal:  Acta Haematol       Date:  1994       Impact factor: 2.195

Review 8.  Current options for the treatment of idiopathic thrombocytopenic purpura.

Authors:  Donald M Arnold; John G Kelton
Journal:  Semin Hematol       Date:  2007-10       Impact factor: 3.851

Review 9.  The pathogenesis of chronic immune thrombocytopenic purpura.

Authors:  Robert McMillan
Journal:  Semin Hematol       Date:  2007-10       Impact factor: 3.851

Review 10.  Rituximab in the treatment of autoimmune haematological disorders.

Authors:  Bernadette Garvey
Journal:  Br J Haematol       Date:  2008-03-03       Impact factor: 6.998

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