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获得性免疫缺陷综合征中的隐孢子虫病:15例尸检病例研究

Cryptosporidiosis in the acquired immunodeficiency syndrome: a study of 15 autopsy cases.

作者信息

Godwin T A

机构信息

Department of Pathology, New York Hospital-Cornell Medical Center, NY 10021.

出版信息

Hum Pathol. 1991 Dec;22(12):1215-24. doi: 10.1016/0046-8177(91)90103-v.

DOI:10.1016/0046-8177(91)90103-v
PMID:1748428
Abstract

The pathologic changes associated with human cryptosporidiosis have not been well characterized. In this report, 15 cases of cryptosporidiosis in acquired immunodeficiency syndrome patients are described. Organisms were found in autopsy tissue specimens in 13 cases, and only in antemortem stool samples in two. Gastrointestinal/hepatobiliary distribution of organisms was as follows: small intestine (13 cases), extrahepatic bile ducts (eight), intrahepatic bile ducts (seven), large intestine (six), pancreas (five), stomach (three), and esophagus (one). At all sites, infection was usually associated with nonspecific reactive epithelial changes, architectural abnormalities such as villous flattening in the small intestine, and interstitial edema with mixed inflammatory cell infiltrates. Presence of organisms and associated mucosal injury were patchy and of variable severity in the intestine. In the biliary tract, injury was commonly diffuse and severe. Pancreatic duct injury was generally mild and often limited to hyperplastic squamous metaplasia. In late-stage acquired immunodeficiency syndrome patients with cryptosporidiosis, widespread infection in the gastrointestinal and biliary systems by this coccidian was more common and severe than previously suggested. Although the mechanisms have yet to be determined, infection usually is accompanied by pathologic changes that may be causally related to pathophysiologic abnormalities, such as diarrhea and malabsorption, and may account for other clinical manifestations of pancreatitis, cholangitis, and obstructive cholestasis.

摘要

与人类隐孢子虫病相关的病理变化尚未得到充分描述。在本报告中,描述了15例获得性免疫缺陷综合征患者的隐孢子虫病。13例在尸检组织标本中发现病原体,2例仅在生前粪便样本中发现。病原体在胃肠道/肝胆系统的分布如下:小肠(13例)、肝外胆管(8例)、肝内胆管(7例)、大肠(6例)、胰腺(5例)、胃(3例)和食管(1例)。在所有部位,感染通常与非特异性反应性上皮变化、结构异常(如小肠绒毛变平)以及伴有混合性炎症细胞浸润的间质水肿有关。病原体的存在和相关的黏膜损伤在肠道中呈斑片状,严重程度不一。在胆道,损伤通常弥漫且严重。胰管损伤一般较轻,常局限于增生性鳞状化生。在晚期获得性免疫缺陷综合征合并隐孢子虫病的患者中,这种球虫在胃肠道和胆道系统中的广泛感染比以前认为的更为常见和严重。虽然其机制尚未确定,但感染通常伴有可能与病理生理异常(如腹泻和吸收不良)有因果关系的病理变化,并且可能是胰腺炎、胆管炎和梗阻性胆汁淤积等其他临床表现的原因。

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