interferon-beta-1b induced autoimmune hemolytic anemia in a patient with ms: a case report

Authors

m saeedi department of neurology, ghaem hospital, mashhad university of medical sciences, iran

m forughipour department of neurology, ghaem hospital, mashhad university of medical sciences, iran

p sasannezhad department of neurology, ghaem hospital, mashhad university of medical sciences, iran

a shoeibi department of neurology, ghaem hospital, ahmadabad blvd, po box: 91766-99199, iran +98-511-8012398, [email protected]; department of neurology, ghaem hospital, ahmadabad blvd, po box: 91766-99199, iran +98-511-8012398, [email protected]

abstract

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Interferon-Beta-1b Induced Autoimmune Hemolytic Anemia in a Patient with MS: A Case Report

A 26-year-old lady with the diagnosis of multiple sclerosis who had received interferon beta1-b for eleven months was visited in MS clinic of our hospital because of icter and fatigue. Laboratory tests showed anemia, indirect hyperbillirubinemia, increased LDH, positive direct and indirect coomb's tests, and increased reticulocyte count and percentage. Other causes of autoimmune hemolytic anemi...

full text

Autoimmune Hemolytic Anemia in a Patient with Probable Ataxia Telangiectasia: A Case Report

Background: Ataxia telangiectasia (AT) is one of the combined immunodeficiency syndromes with immunologic, neurologic, endocrinologic, hepatic and cutaneous abnormalities. Regarding the fact that autoimmune disorders; such as autoimmune hemolytic anemia (AIHA), are not generally expected in the course of AT, we present a patient with an unusual presentation of these two conditions. Case present...

full text

autoimmune hemolytic anemia in a patient with probable ataxia telangiectasia: a case report

background: ataxia telangiectasia (at) is one of the combined immunodeficiency syndromes with immunologic, neurologic, endocrinologic, hepatic and cutaneous abnormalities. regarding the fact that autoimmune disorders; such as autoimmune hemolytic anemia (aiha), are not generally expected in the course of at, we present a patient with an unusual presentation of these two conditions. case present...

full text

Concurrent Atypical Hemolytic Uremic Syndrome and Autoimmune Hemolytic Anemia: a case report

Background: Atypical hemolytic uremic syndrome (aHUS) is a life-threatening and scarce disorder characterized by acute renal failure and disease, non-immune microangiopathic hemolytic anemia and thrombocytopenia, leading to end-stage renal failure or death, and consequently maybe accompanying by extra renal manifestations. Case report: We reported aHUS accompanied by autoimmune hemolytic anemi...

full text

Autoimmune hemolytic anemia in a patient with probable ataxia telangiectasia: a case report.

BACKGROUND Ataxia telangiectasia (AT) is one of the combined immunodeficiency syndromes with immunologic, neurologic, endocrinologic, hepatic and cutaneous abnormalities. Regarding the fact that autoimmune disorders; such as autoimmune hemolytic anemia (AIHA), are not generally expected in the course of AT, we present a patient with an unusual presentation of these two conditions. CASE PRESEN...

full text

Successful Treatment of Refractory Autoimmune Hemolytic Anemia (AIHA) in a Child, Based on Iranian Traditional Medicine: A Case Report

Autoimmune hemolytic anemia (AIHA) is a heterogeneous and relatively unknown disease caused by premature immune destruction of red blood cells. While its occurrence is uncommon among children, it is sometimes severe and resistant to treatment. The warm-reactive type contains 70% to 80% of all cases, in which the first-line treatment is considered to be a steroid. Moreover, splenectomy, rituxima...

full text

My Resources

Save resource for easier access later


Journal title:
iranian red crescent medical journal

جلد ۱۳، شماره ۳، صفحات ۲۱۰-۲۱۲

Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023