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Article: Alemtuzumab induced complete remission of autoimmune hemolytic anemia refractory to corticosteroids, splenectomy and rituximab.
Title | Alemtuzumab induced complete remission of autoimmune hemolytic anemia refractory to corticosteroids, splenectomy and rituximab. |
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Authors | |
Issue Date | 2006 |
Publisher | Fondazione Ferrata Storti. |
Citation | Haematologica., 2006, v. 91 n. 5 suppl., p. ECR13 How to Cite? |
Abstract | A 58-year-old man with warm-antibody-mediated autoimmune hemolytic anemia (AIHA) refractory to prednisolone, azathioprine, splenectomy, rituximab and combination chemotherapy, and with unacceptably high transfusion requirement, was treated with alemtuzumab. After a cumulative dose of 883 mg of alemtuzumab, the AIHA remitted completely, with normalization of hemoglobin and transfusion-independence. The major side effect was reactivation of cytomegalovirus, which was controlled with intravenous and oral ganciclovir. This case showed that alemtuzumab might be of use in therapy-refractory AIHA. |
Persistent Identifier | http://hdl.handle.net/10722/162995 |
ISSN | 2023 Impact Factor: 8.2 2023 SCImago Journal Rankings: 2.490 |
DC Field | Value | Language |
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dc.contributor.author | Cheung, WW | en_US |
dc.contributor.author | Hwang, GY | en_US |
dc.contributor.author | Tse, E | en_US |
dc.contributor.author | Kwong, YL | en_US |
dc.date.accessioned | 2012-09-05T05:26:21Z | - |
dc.date.available | 2012-09-05T05:26:21Z | - |
dc.date.issued | 2006 | en_US |
dc.identifier.citation | Haematologica., 2006, v. 91 n. 5 suppl., p. ECR13 | en_US |
dc.identifier.issn | 1592-8721 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162995 | - |
dc.description.abstract | A 58-year-old man with warm-antibody-mediated autoimmune hemolytic anemia (AIHA) refractory to prednisolone, azathioprine, splenectomy, rituximab and combination chemotherapy, and with unacceptably high transfusion requirement, was treated with alemtuzumab. After a cumulative dose of 883 mg of alemtuzumab, the AIHA remitted completely, with normalization of hemoglobin and transfusion-independence. The major side effect was reactivation of cytomegalovirus, which was controlled with intravenous and oral ganciclovir. This case showed that alemtuzumab might be of use in therapy-refractory AIHA. | en_US |
dc.language | eng | en_US |
dc.publisher | Fondazione Ferrata Storti. | - |
dc.relation.ispartof | Haematologica. | en_US |
dc.subject.mesh | Anemia, Hemolytic, Autoimmune - Complications - Drug Therapy - Surgery - Therapy | en_US |
dc.subject.mesh | Antibodies, Monoclonal - Adverse Effects - Therapeutic Use | en_US |
dc.subject.mesh | Antibodies, Monoclonal, Humanized | en_US |
dc.subject.mesh | Antibodies, Monoclonal, Murine-Derived | en_US |
dc.subject.mesh | Antibodies, Neoplasm - Adverse Effects - Therapeutic Use | en_US |
dc.subject.mesh | Antigens, Cd - Immunology | en_US |
dc.subject.mesh | Antigens, Neoplasm - Immunology | en_US |
dc.subject.mesh | Antiviral Agents - Therapeutic Use | en_US |
dc.subject.mesh | Azathioprine - Therapeutic Use | en_US |
dc.subject.mesh | Blood Transfusion | en_US |
dc.subject.mesh | Cytomegalovirus - Drug Effects - Physiology | en_US |
dc.subject.mesh | Cytomegalovirus Infections - Complications - Drug Therapy | en_US |
dc.subject.mesh | Drug Resistance | en_US |
dc.subject.mesh | Ganciclovir - Analogs & Derivatives - Therapeutic Use | en_US |
dc.subject.mesh | Glycoproteins - Immunology | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunosuppressive Agents - Adverse Effects - Therapeutic Use | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Prednisolone - Therapeutic Use | en_US |
dc.subject.mesh | Remission Induction | en_US |
dc.subject.mesh | Splenectomy | en_US |
dc.subject.mesh | Viremia - Complications - Drug Therapy | en_US |
dc.subject.mesh | Virus Activation - Drug Effects | en_US |
dc.title | Alemtuzumab induced complete remission of autoimmune hemolytic anemia refractory to corticosteroids, splenectomy and rituximab. | en_US |
dc.type | Article | en_US |
dc.identifier.email | Tse, E:ewctse@hku.hk | en_US |
dc.identifier.email | Kwong, YL:ylkwong@hku.hk | en_US |
dc.identifier.authority | Tse, E=rp00471 | en_US |
dc.identifier.authority | Kwong, YL=rp00358 | en_US |
dc.description.nature | link_to_OA_fulltext | en_US |
dc.identifier.pmid | 16709521 | - |
dc.identifier.scopus | eid_2-s2.0-33745941145 | en_US |
dc.identifier.hkuros | 122742 | - |
dc.identifier.volume | 91 | en_US |
dc.identifier.issue | 5 suppl. | en_US |
dc.identifier.spage | ECR13 | en_US |
dc.identifier.scopusauthorid | Cheung, WW=8615134400 | en_US |
dc.identifier.scopusauthorid | Hwang, GY=14038936500 | en_US |
dc.identifier.scopusauthorid | Tse, E=7005019454 | en_US |
dc.identifier.scopusauthorid | Kwong, YL=7102818954 | en_US |
dc.identifier.issnl | 0390-6078 | - |