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Successful Treatment of a Korean Infant with Giant Cell Hepatitis with Autoimmune Hemolytic Anemia Using Rituximab

Kim YH, Kim JW, Lee EJ, Kang GH, Kang HJ, Moon JS, Ko JS

Giant cell hepatitis with autoimmune hemolytic anemia (AHA) is a rare disease of infancy characterized by the presence of both Coombs-positive hemolytic anemia and progressive liver disease with giant cell...
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Treatment of autoimmune hemolytic anemia: real world data from a reference center in Mexico

Jaime-Pérez JC, Aguilar-Calderón P, Salazar-Cavazos L, Gómez-De León A, Gómez-Almaguer D

BACKGROUND: Warm autoimmune hemolytic anemia (w-AIHA) is an uncommon disease with heterogeneous response to treatment. Steroids are the standard treatment at diagnosis, whereas rituximab has recently been recommended as the...
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Anesthetic Experience of Cesarean Section in Evans Syndrome

Cho A

Evans syndrome is an uncommon condition defined by the combination of immune thrombocytopenia and autoimmune hemolytic anemia in the absence of known underlying cause. Association of Evans syndrome with pregnancy...
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Splenic myeloid metaplasia in warm autoimmune hemolytic anemia (wAIHA): a retrospective study

Anguiano-Álvarez VM, Hernández-Company A, Hamdan-Pérez N, Montante-M D, Zúñiga-Tamayo DA, Rodríguez-Rodríguez S, Pomerantz , Tuna-Aguilar EJ

BACKGROUND: Splenic myeloid metaplasia (SMM) is a kind of extramedullary hematopoiesis, whereas its clinical significance in wAIHA remains unclear. The aim of this study is evaluating the frequency and clinical...
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Quetiapine Induced Autoimmune Hemolytic Anemia in a Child Patient: A Case Report

Arici A, Altun H, Acipayam C

Autoimmune hemolytic anemia is a disease characterized with destruction of erythrocytes as a result of antibody produce against patient's own erythrocytes and anemia. Autoimmune hemolytic anemia can be roughly stratified...
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Treatment and response of autoimmune cytopenia occurring after allogeneic hematopoietic cell transplantation in children

Hwang-Bo S, Kim SK, Lee JW, Jang PS, Chung NG, Jeong DC, Cho B, Kim HK

BACKGROUND: Autoimmune cytopenia (AIC) is a rare complication of allogeneic hematopoietic cell transplantation (HCT). In this study, we reviewed the diagnosis, treatment and response to therapy for pediatric patients with...
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Warm autoimmune hemolytic anemia: experience from a single referral center in Mexico City

Alonso HC, Manuel AA, Amir CG, Sergio RR, Allan P, Xavier LK, Juventina

BACKGROUND: Autoimmune hemolytic anemia (AIHA) is characterized by an autoimmune-mediated destruction of red blood cells. Warm AIHA (wAIHA) represents 60% of AIHA cases and is associated with the positive detection...
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Prognostic factors and efficacy of human intravenous immunoglobulin G in dogs with idiopathic immune-mediated hemolytic anemia: a retrospective study

Park SY, Kim H, Kang BT, Kang JH, Yang MP

This study was conducted to determine the effect of treatment with intravenous human immunoglobulin G (hIVIgG) on outcome in dogs with idiopathic immune-mediated hemolytic anemia (IMHA), and to identify prognostic...
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Clinical characteristics and treatment outcomes of primary autoimmune hemolytic anemia: a single center study from South India

Prabhu R, Bhaskaran , Shenoy V, G R, Sidharthan N

BACKGROUND: Autoimmune hemolytic anemia (AIHA) is a less recognized, potentially fatal condition. There is a scarcity of data on clinicoserological characteristics and response to therapy concerning this disease from South...
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Autoimmune Hemolytic Anemia after Intravenous Immunoglobulin Therapy in a Child with Kawasaki Disease

Moon JW, Lee SH, Oh YK, Choi DY, Yu ST

Kawasaki disease (KD) can cause acquired heart disease and systemic vasculitis in children. It is treated with intravenous immunoglobulin (IVIG). A significant complication is development of coronary artery lesions such...
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Retrospective Clinical Analysis of Treatment for Primary Warm Autoimmune Hemolytic Anemia

Moon HS, Park C

BACKGROUND: Primary warm autoimmune hemolytic anemia (AIHA) is a relatively rare hematologic disorder resulting from autoantibody production against red blood cells. There has been very few studies about primary warm...
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Use of Splenectomy to Treat Evans Syndrome Following an ABO-Matched Liver Transplant

Yun JH, Ahn JH, Cho DH, Kim T, Song GW, Lee SG, Lee KH

Evans syndrome is a rare complication that develops in adults after liver transplantation. The possible etiologies include ABO mismatch, viral infection, post-transplantation lymphoproliferative disease, graft-versus-host disease, and the use of...
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Therapeutic Plasma Exchange for a Patient with Severe Cold Agglutinin Disease

Yang N, Park S, Chung HS, Mun YC, Yu S, Kwon MJ, Woo HY, Oh S, Lee M

Cold agglutinin disease is a kind of autoimmune hemolytic anemia, caused by cold agglutinin, serum autoantibodies activated at reduced body temperatures to produce red blood cell agglutination and hemolysis. In...
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Acute Ischemic Stroke Showing Microembolic Signals in a Patient With Autoimmune Hemolytic Anemia

Kim HJ, Shin HS, Lee DH

  • KMID: 2343529
  • J Korean Neurol Assoc.
  • 2014 Aug;32(3):182-185.
Autoimmune hemolytic anemia (AIHA) can be considered in the differential diagnosis of hemolytic anemia with a concomitant cerebral infarction. We report a 79-year-old woman who was stuporous at presentation, and...
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Pure red-cell aplasia and autoimmune hemolytic anemia in a patient with acute hepatitis A

Chang HJ, Sinn DH, Cho SG, Oh TH, Jeon TJ, Shin WC, Choi WC

Pure red cell aplasia (PRCA) and autoimmune hemolytic anemia (AIHA) have rarely been reported as an extrahepatic manifestation of acute hepatitis A (AHA). We report herein a case of AHA...
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Mycophenolate Mofetil for Treatment of Autoimmune Hemolytic Anemia and Nephrotic Syndrome after Cord Blood Transplantation

Lee JM, Kim SY, Kim YK

We report on a 2-year-old girl who developed autoimmune hemolytic anemia, which occurred with minimal change nephrotic syndrome 3 months after umbilical cord blood transplantation for acute megakaryocytic leukemia. Because...
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Autoimmune Hemolytic Anemia after Aplastic Crisis due to Parvovirus B19 Infection in a Patient with Hereditary Spherocytosis

Song SA, Lee MY, Kim SH, Lee JY, Oh SH, Shin JH, Kim HR, Jun KR, Lee JN

  • KMID: 2312200
  • Lab Med Online.
  • 2012 Jul;2(3):166-169.
Hereditary spherocytosis (HS) is a genetic disorder characterized by the production and destruction of spherocytes due to a deficiency of red cell membrane cytoskeletal proteins, resulting in the clinical presentation...
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Clinical features and outcomes of autoimmune hemolytic anemia: a retrospective analysis of 32 cases

Baek SW, Lee MW, Ryu HW, Lee KS, Song IC, Lee HJ, Yun HJ, Kim S, Jo DY

BACKGROUND: There has been no report on the clinical features or natural history of autoimmune hemolytic anemia (AIHA) in the Korean adult population. This study retrospectively analyzed the clinical characteristics...
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Splenic infarction in a patient with autoimmune hemolytic anemia and protein C deficiency

Park MY, Kim JA, Yi SY, Chang SH, Um TH, Lee HR

Splenic infarction is most commonly caused by cardiovascular thromboembolism; however, splenic infarction can also occur in hematologic diseases, including sickle cell disease, hereditary spherocytosis, chronic myeloproliferative disease, leukemia, and lymphoma....
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Autoimmune hemolytic anemia during PEG-interferon and ribavirin treatment for hepatitis C

Yu JY, Kim CW, Kim JD, Kwon JH, Jang JW, Yoon SK, Lee CD

  • KMID: 2142941
  • Korean J Med.
  • 2010 Feb;78(2):226-230.
The current best treatment for HCV infection is combination therapy with PEG-interferon and ribavirin. This combination therapy has markedly increased the number of sustained virologic responders but is associated with...
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