1.A 20-Year-Old Woman with Hashimoto's Thyroiditis and Evans' Syndrome.
Mi Yeon KANG ; Jong Ryeal HAHM ; Tae Sik JUNG ; Gyeong Won LEE ; Deok Ryong KIM ; Myoung Hee PARK
Yonsei Medical Journal 2006;47(3):432-436
Here we report the case of a 20-year-old female patient previously diagnosed with Hashimoto's thyroiditis and overt hypothyroidism, and who had been taking synthetic thyroxine (100micro/day) for eight months. She experienced intermittent dizziness and generalized weakness, and was diagnosed as having severe autoimmune hemolytic anemia (AIHA). We prescribed prednisolone treatment and continued synthetic thyroxine administration. Two years and five months later, she developed idiopathic thrombocytopenic purpura (ITP) and was diagnosed with Evans' syndrome. Thereafter, laparoscopic splenectomy was performed because her autoimmune hemolytic anemia was refractory and dependent on steroid therapy. The HLA genotypes of the patient were HLA-A*020101/A*2602, HLA-B*270502/B*5401, HLA-Cw*0102/Cw*020202, HLA-DRB1*0404/DRB1*0405, and HLA-DQB1*0302/DQ B1*0401. Hashimoto's thyroiditis is often associated with other nonendocrine autoimmune diseases, and antithyroid antibodies are frequently observed in Evans' syndrome (coexistence of AIHA and ITP). However, there is no report of Evans' syndrome developing in patients with overt hypothyroidism and Hashimoto's thyroiditis. This case suggests that three autoimmune diseases (AIHA, ITP, and Hashimoto's thyroiditis) might share a common immunogenetic pathway in pathogenesis.
Purpura, Thrombocytopenic/blood/*complications
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Humans
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Hashimoto Disease/*complications/radionuclide imaging
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Female
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Anemia, Hemolytic, Autoimmune/blood/*complications
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Adult
2.A Case of Autoimmune Hemolytic Anemia Associated with an Ovarian Teratoma.
Ickkeun KIM ; Jue Yong LEE ; Jung Hye KWON ; Joo Young JUNG ; Hun Ho SONG ; Young Iee PARK ; Eusun RO ; Kyung Chan CHOI
Journal of Korean Medical Science 2006;21(2):365-367
Autoimmune hemolytic anemia associated with an ovarian teratoma is a very rare disease. However, treating teratoma is the only method to cure the hemolytic anemia, so it is necessary to include ovarian teratoma in the differential diagnosis of autoimmune hemolytic anemia. We report herein on a case of a young adult patient who had severe autoimmune hemolytic anemia that was induced by an ovarian teratoma. A 25-yr-old woman complained of general weakness and dizziness for 1 week. The hemoglobin level was 4.2 g/dL, and the direct and indirect antiglobulin tests were all positive. The abdominal computed tomography scan revealed a huge left ovarian mass, and this indicated a teratoma. She was refractory to corticosteroid therapy; however, after surgical resection of the ovarian mass, the hemoglobin level and the reticulocyte count were gradually normalized. The mass was well encapsulated and contained hair and teeth. She was diagnosed as having autoimmune hemolytic anemia associated with an ovarian teratoma. To the best of our knowledge, this is the first such a case to be reported in Korea.
Teratoma/*complications/diagnosis/surgery
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Ovarian Neoplasms/*complications/diagnosis/surgery
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Humans
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Female
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Diagnosis, Differential
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Blood Transfusion
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Anemia, Hemolytic, Autoimmune/diagnosis/*etiology/therapy
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Adult
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Adrenal Cortex Hormones/therapeutic use
3.Coinfection of hepatitis A virus genotype IA and IIIA complicated with autoimmune hemolytic anemia, prolonged cholestasis, and false-positive immunoglobulin M anti-hepatitis E virus: a case report.
Hee Sup KIM ; Sook Hyang JEONG ; Je Hyuck JANG ; Hyung Joon MYUNG ; Jin Wook KIM ; Soo Mee BANG ; Sang Hoon SONG ; Haeryoung KIM ; Hae Sun YUN
The Korean Journal of Hepatology 2011;17(4):323-327
A 37-year-old male presented with fever and jaundice was diagnosed as hepatitis A complicated with progressive cholestasis and severe autoimmune hemolytic anemia. He was treated with high-dose prednisolone (1.5 mg/kg), and eventually recovered. His initial serum contained genotype IA hepatitis A virus (HAV), which was subsequently replaced by genotype IIIA HAV. Moreover, at the time of development of hemolytic anemia, he became positive for immunoglobulin M (IgM) anti-hepatitis E virus (HEV). We detected HAV antigens in the liver biopsy specimen, while we detected neither HEV antigen in the liver nor HEV RNA in his serum. This is the first report of hepatitis A coinfected with two different genotypes manifesting with autoimmune hemolytic anemia, prolonged cholestasis, and false-positive IgM anti-HEV.
Adult
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Anemia, Hemolytic, Autoimmune/*diagnosis/drug therapy/etiology
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Anti-Inflammatory Agents/therapeutic use
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Cholestasis/*diagnosis/drug therapy/pathology
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Coinfection/*diagnosis
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Genotype
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Hepatitis A/complications/*diagnosis/genetics
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Hepatitis E/complications/*diagnosis/genetics
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Humans
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Immunoglobulin M/blood
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Liver/pathology/virology
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Male
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Prednisolone/therapeutic use
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RNA, Viral/blood