Prolonged remission after splenectomy for refractory Evans syndrome--a case report and literature review.
Southeast Asian J Trop Med Public Health
;
2005 May; 36(3): 762-4
Article
in English
| IMSEAR
| ID: sea-32242
ABSTRACT
We describe a patient with Evans syndrome (autoimmune hemolytic anemia and autoimmune thrombocytopenia) who was refractory to steroids and intravenous immunoglobulin. She responded to splenectomy and has remained in clinical remission for 3 years. In the majority of cases, splenectomy rarely induces a durable remission but it may be beneficial in a small group of patients, hence should be considered as alternative therapy in the management of these patients.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Recurrence
/
Splenectomy
/
Syndrome
/
Blood Transfusion
/
Remission Induction
/
Female
/
Humans
/
Prednisone
/
Adolescent
/
Purpura, Thrombocytopenic, Idiopathic
Language:
English
Journal:
Southeast Asian J Trop Med Public Health
Year:
2005
Type:
Article
Similar
MEDLINE
...
LILACS
LIS