Autoimmune hemolytic anemia causes: Difference between revisions
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{{Autoimmune hemolytic anemia}} | {{Autoimmune hemolytic anemia}} | ||
{{CMG}} '''Assosciate Editor(s)-In-Chief:''' [[User: Prashanthsaddala|Prashanth Saddala M.B.B.S]] | {{CMG}} '''Assosciate Editor(s)-In-Chief:''' [[User: Prashanthsaddala|Prashanth Saddala M.B.B.S]]; {{shyam}} | ||
==Overview== | ==Overview== |
Revision as of 17:16, 17 March 2018
Autoimmune hemolytic anemia Microchapters |
Differentiating Autoimmune hemolytic anemia from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Assosciate Editor(s)-In-Chief: Prashanth Saddala M.B.B.S; Shyam Patel [2]
Overview
Causes
Primary autoimmune hemolytic anemia
Secondary autoimmune hemolytic anemia
Secondary autoimmune hemolytic anemia is due to an underlying condition, such as malignancy. This accounts for 50% of cases of warm autoimmune hemolytic anemia. A variety of malignancies can cause secondary autoimmune hemolytic anemia including chronic lymphocytic leukemia (CLL) and non-Hodgkin's lymphoma. Systemic autoimmune conditions can also cause secondary autoimmune hemolytic anemia. These conditions include systemic lupus erythematosus, hypothyroidism, Sjogren's syndrome, and inflammatory bowel disease.[1]
References
- ↑ Berentsen S (2015). "Role of Complement in Autoimmune Hemolytic Anemia". Transfus Med Hemother. 42 (5): 303–10. doi:10.1159/000438964. PMC 4678321. PMID 26696798.