Hereditary Spherocytosis in a Middle-aged Man Complicated with Common Bile Duct Stones
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- Sawahara Hiroaki
- Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Japan
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- Iwamuro Masaya
- Department of General Medicine, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Japan
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- Harada Ryo
- Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Japan
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- Yoshioka Masao
- Department of Internal Medicine, Okayama Saiseikai General Hospital, Japan
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- Niguma Takefumi
- Department of Surgery, Okayama Saiseikai General Hospital, Japan
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- Mimura Tetsushige
- Department of Surgery, Okayama Saiseikai General Hospital, Japan
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- Yamamoto Kazuhide
- Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Japan
書誌事項
- 公開日
- 2015
- 資源種別
- journal article
- DOI
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- 10.2169/internalmedicine.54.4812
- 公開者
- 一般社団法人 日本内科学会
この論文をさがす
説明
Hereditary spherocytosis is the most common form of hemolytic anemia and is characterized by spherical, osmotically fragile erythrocytes that are selectively trapped by the spleen. Hereditary spherocytosis is typically diagnosed in childhood. We herein experienced a rare case of hereditary spherocytosis diagnosed in middle age. The patient presented with cholelithiasis and hyperbilirubinemia. He had no anemia and was asymptomatic with mild splenomegaly. In the differential diagnosis of these symptoms, the possibility of hereditary spherocytosis should be considered, even in patients who are middle-aged and lack anemia.<br>
収録刊行物
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- Internal Medicine
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Internal Medicine 54 (12), 1509-1512, 2015
一般社団法人 日本内科学会
