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Autoimmune Hemolytic Anemia Associated with Primary Biliary Cirrhosis
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- Omata Fumio
- St Luke's International Hospital
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- Sato Shinkichi
- Department of Pathology, Tokai University School of Medicine
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- Tokuda Yasuharu
- St Luke's International Hospital
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- Takahashi Osamu
- St Luke's International Hospital
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- Fukui Tsuguya
- St Luke's International Hospital
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Description
ABSTRACT : Both primary biliary cirrhosis (PBC) and autoimmune hemolytic anemia (AIHA) are uncommon diseases. Immunological dysregulation is suggested as a causative factor for both diseases. We report a 77-year-old woman who suffered from warm type AIHA complicated by PBC. Her direct antiglobulin test was positive for IgG, and negative for C3. Both anti-mitochondrial antibody and its M2 component were detected. Both alkaline phosphatase (Alp) and IgM were elevated in the serum. She was initially treated with steroids for 8 months. Her steroids were discontinued when she underwent a laparoscopic splenectomy. Ursodeoxycholic acid was discontinued due to an allergic skin reaction. Her Alp improved with bezafibrate.
Journal
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- General Medicine
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General Medicine 9 (2), 65-70, 2008
Japan Primary Care Association
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Details 詳細情報について
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- CRID
- 1390282680165911168
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- NII Article ID
- 10029403662
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- NII Book ID
- AA11571086
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- ISSN
- 18836011
- 13460072
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- Text Lang
- en
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
- OpenAIRE
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- Abstract License Flag
- Disallowed