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[获得性免疫缺陷综合征患者中由播散性非结核分枝杆菌病引起的巨大进行性肝脾肿大]

[Massive and progressive hepatosplenomegaly caused by disseminated nontuberculous mycobacteriosis in a patient with acquired immunodeficiency syndrome].

作者信息

Hagiwara T, Amano K, Sugimura D, Isogai N, Arai M, Fukutake K, Kojima H, Shimada H

机构信息

Department of Clinical Pathology, Tokyo Medical College, Japan.

出版信息

Kekkaku. 1995 Jul;70(7):423-9.

PMID:7564051
Abstract

A 28-year-old hemophilia A patient was admitted to our hospital in July, 1991 because of high fever, chronic diarrhea and anemia. The patient had been recognized as a asymptomatic carrier of human immunodeficiency virus (HIV) in 1985 and had developed Pneumocystis carinii pneumonia and had been diagnosed as acquired immunodeficiency syndrome (AIDS) in 1990. Hematologic laboratory examinations on admission revealed pancytopenia and a CD4+ cell count of 3/mm3. X-ray findings of chest and abdomen were normal and bacterial cultures of sputum, urine, blood, stool, cerebrospinal fluid and bone marrow yielded no pathogenic microorganisms. Microscopical examination of the stained specimens showed no acid-fast bacilli. On his fifth hospital day, his liver and spleen enlarged markedly and an abdominal CT scan obtained on the 13th day revealed high-grade hepatosplenomegaly. Administration of several kinds of antibiotics, antifungal agents, antiviral agents, antituberculous agents and gamma-globulin medicines did not relieve the symptoms. On the 28th day the patient had developed a subarachnoid hemorrhage and died five days later. Retrospectively all cultures for acid-fast bacilli of the specimens on his admission yielded nontuberculous mycobacteria. The bacteria were identified as Mycobacterium avium by polymerase chain reaction and his disease was eventually diagnosed as disseminated Mycobacterium avium complex (MAC) infection. The liver and spleen weighed 2,660 g and 1,840 g respectively at autopsy. Although hepatosplenomegaly is commonly recognized in AIDS patients with disseminated MAC infection, such massive and rapid enlargement has been rarely observed. This case study emphasize the importance of diagnosis and rapid treatment at the early stage of MAC infection.

摘要

一名28岁的甲型血友病患者于1991年7月因高热、慢性腹泻和贫血入院。该患者在1985年被确认为人类免疫缺陷病毒(HIV)无症状携带者,1990年患卡氏肺孢子虫肺炎并被诊断为获得性免疫缺陷综合征(AIDS)。入院时血液学实验室检查显示全血细胞减少,CD4+细胞计数为3/mm³。胸部和腹部X线检查结果正常,痰、尿、血、粪便、脑脊液和骨髓的细菌培养均未发现致病微生物。染色标本的显微镜检查未发现抗酸杆菌。在他住院的第五天,肝脏和脾脏明显肿大,第13天进行的腹部CT扫描显示高度肝脾肿大。使用多种抗生素、抗真菌药、抗病毒药、抗结核药和γ-球蛋白药物均未能缓解症状。第28天患者发生蛛网膜下腔出血,五天后死亡。回顾性分析,其入院时标本的所有抗酸杆菌培养均检出非结核分枝杆菌。通过聚合酶链反应将细菌鉴定为鸟分枝杆菌,其疾病最终被诊断为播散性鸟分枝杆菌复合群(MAC)感染。尸检时肝脏和脾脏重量分别为2660克和1840克。虽然肝脾肿大在播散性MAC感染的艾滋病患者中很常见,但如此巨大和迅速的肿大很少见。本病例研究强调了MAC感染早期诊断和快速治疗的重要性。

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