Eosinophilic cholecystitis: A rare manifestation of hypereosinophilic syndrome

被引:0
|
作者
Park, Jae-Hyun [1 ]
Kim, Byoung-Hoon [1 ]
Kim, Mi-Kang [1 ]
Lee, Jae-Eun [1 ]
Kim, Kwang-Taek [1 ]
Yoo, Jun-Jae [1 ]
Kim, Hee-Jun [1 ]
Jung, Sung-Won [1 ]
Kim, Cheol-Hong [1 ,2 ]
Hyun, In-Gyu [1 ,2 ]
Choi, Jeong-Hee [1 ,2 ]
机构
[1] Hallym Univ, Coll Med, Dept Internal Med, Chunchon, South Korea
[2] Hallym Univ, Coll Med, Lung Res Inst, Chunchon, South Korea
来源
关键词
Hypereosinophilic syndrome; Cholecystitis; Cholangitis;
D O I
10.4168/aard.2014.2.3.222
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Eosinophilic cholecystitis (EC) is a rare form of acute cholecystitis, of which diagnosis is based on classical symptoms of cholecystitis with a presence of > 90% eosinophilic infiltration within the gall bladder. EC rarely manifests in idiopathic hypereosinophilic syndrome (IHES). Here, we report two cases of EC with IHES. One is a 57-year-old male who presented with acute right upper quadrant (RUQ) pain, jaundice and fever. The initial peripheral blood eosinophil count was 2,070/mm(3), and further elevated to 12,590/mm(3). Acute acalculous cholecystitis with cholangitis was confirmed by computed tomography (CT). He improved with endocopic nasobiliary drainage and antibiotic therapy. The other is a 64-year-old female who presented with acute RUQ pain. She also complained of dyspnea and tingling sensation of both hands and feet. The initial peripheral blood eosinophil count was 10,400/mm(3). Abdominal CT revealed findings suggestive of acute acalculous cholecystitis. She improved with systemic glucocorticosteroid therapy. No other causes of hypereosinophilia were found in either patients. Thus, cholecystectomy may not be mandatory for the treatment of EC with IHES.
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收藏
页码:222 / 226
页数:5
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