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与人类免疫缺陷病毒感染相关的杆菌性肝紫癜的临床和病理特征。

Clinical and pathological features of bacillary peliosis hepatis in association with human immunodeficiency virus infection.

作者信息

Perkocha L A, Geaghan S M, Yen T S, Nishimura S L, Chan S P, Garcia-Kennedy R, Honda G, Stoloff A C, Klein H Z, Goldman R L

机构信息

Department of Pathology, University of California, San Francisco.

出版信息

N Engl J Med. 1990 Dec 6;323(23):1581-6. doi: 10.1056/NEJM199012063232302.

Abstract

BACKGROUND

Peliosis hepatis is characterized by cystic, blood-filled spaces in the liver and is seen in patients with chronic infections or advanced cancer and as a consequence of therapy with anabolic steroids. Cutaneous bacillary angiomatosis is a bacterial infection that occurs in patients with human immunodeficiency virus (HIV) infection; its histologic appearance is that of a pseudoneoplastic vascular proliferation.

METHODS

We studied liver tissue from eight HIV-infected patients with peliosis hepatis, two of whom also had cutaneous bacillary angiomatosis. For comparison we examined tissue from four patients who had peliosis hepatis without HIV infection. Tissues were examined histologically on routine sections and with special stains and electron microscopy.

RESULTS

The histologic features seen in peliosis hepatis associated with HIV infection, but not in the four cases unrelated to HIV infection, were myxoid stroma and clumps of a granular purple material that on Warthin-Starry staining and electron microscopy proved to be bacilli. The bacilli, which could not be cultured, were morphologically identical to those found in the skin lesions of cutaneous bacillary angiomatosis. The clinical courses of two of the patients with this "bacillary peliosis hepatis" indicate that it responds to antibiotic treatment.

CONCLUSIONS

HIV-associated bacillary peliosis hepatis is an unusual, treatable opportunistic infection, probably caused by the same organism that causes cutaneous bacillary angiomatosis. Our failure to find bacilli in non-HIV-associated cases implies that other pathogenetic mechanisms may also be responsible for peliosis hepatis.

摘要

背景

肝紫癜的特征是肝脏出现充满血液的囊性间隙,可见于慢性感染或晚期癌症患者以及接受合成代谢类固醇治疗的患者。皮肤杆菌性血管瘤病是一种发生在人类免疫缺陷病毒(HIV)感染患者中的细菌感染;其组织学表现为假肿瘤性血管增生。

方法

我们研究了8例HIV感染且患有肝紫癜的患者的肝组织,其中2例还患有皮肤杆菌性血管瘤病。作为对照,我们检查了4例无HIV感染但患有肝紫癜的患者的组织。对组织进行常规切片的组织学检查、特殊染色及电子显微镜检查。

结果

与HIV感染相关的肝紫癜中所见的组织学特征,在4例与HIV感染无关的病例中未见到,这些特征包括黏液样基质和颗粒状紫色物质团块,经Warthin-Starry染色和电子显微镜检查证实为杆菌。这些无法培养的杆菌在形态上与皮肤杆菌性血管瘤病皮肤病变中发现的杆菌相同。两名患有这种“杆菌性肝紫癜”患者的临床病程表明,该病对抗生素治疗有反应。

结论

HIV相关的杆菌性肝紫癜是一种不常见的、可治疗的机会性感染,可能由导致皮肤杆菌性血管瘤病的同一病原体引起。我们在非HIV相关病例中未发现杆菌,这意味着其他发病机制也可能导致肝紫癜。

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