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播散性弓形虫病。免疫功能低下宿主中的不寻常表现。

Disseminated toxoplasmosis. Unusual presentations in the immunocompromised host.

作者信息

Arnold S J, Kinney M C, McCormick M S, Dummer S, Scott M A

机构信息

Department of Pathology, Vanderbilt University Medical Center, Nashville, Tenn. 27232-5310, USA.

出版信息

Arch Pathol Lab Med. 1997 Aug;121(8):869-73.

PMID:9278617
Abstract

OBJECTIVE

Owing to the increasing number of patients with acquired immunodeficiency syndrome and immunosuppressed transplant patients, disseminated Toxoplasma gondii has emerged as a potentially fatal pathogen. Common presentations include encephalitis, pneumonia, and myocarditis. The objective of this report is to describe the clinical course, histologic features, and outcome in two immunocompromised patients with disseminated toxoplasmosis presenting with parasitemia and panniculitis.

MATERIALS AND METHODS

Two cases of disseminated toxoplasmosis presenting with parasitemia (patient 1) and panniculitis (patient 2) were retrieved from the clinical, surgical, and autopsy pathology archives of Vanderbilt University Medical Center, Nashville, Tenn. The histology and diagnostic approaches used are reported. Charts were reviewed for primary diagnosis, therapy protocols, clinical presentation of infection, and outcome.

RESULTS

Patient 1 developed a clinically unexplained sepsis syndrome shortly after heart transplantation; T gondii parasitemia was diagnosed by examination of peripheral blood smears. The diagnosis was confirmed at autopsy. Patient 2 was a child undergoing induction chemotherapy for lymphoma who developed rapidly progressive neurologic deterioration accompanied by a maculopapular skin rash; T gondii panniculitis was diagnosed retrospectively when histologic examination was combined with immunohistochemistry. Autopsies performed in both cases confirmed widely disseminated infection.

CONCLUSIONS

Disseminated toxoplasmosis should be considered in the differential diagnosis of immunocompromised patients with culture-negative sepsis syndrome, particularly if combined with neurologic, respiratory, or unexplained skin lesions. Examination of Wright's-stained peripheral blood smears or antitoxoplasma immunoperoxidase studies of skin biopsies may be diagnostic and allow rapid initiation of antibiotic therapy. Autopsy findings contributed to both of our cases by documenting the wide-spread heavy parasite burden and demonstrating numerous diagnostic T gondii cyst forms.

摘要

目的

由于获得性免疫缺陷综合征患者和免疫抑制移植患者数量不断增加,播散性弓形虫病已成为一种潜在的致命病原体。常见表现包括脑炎、肺炎和心肌炎。本报告的目的是描述两名免疫功能低下的播散性弓形虫病患者的临床病程、组织学特征及结局,这两名患者表现为寄生虫血症和脂膜炎。

材料与方法

从田纳西州纳什维尔范德比尔特大学医学中心的临床、外科及尸检病理档案中检索出两例播散性弓形虫病患者,其中一例表现为寄生虫血症(患者1),另一例表现为脂膜炎(患者2)。报告了所采用的组织学和诊断方法。查阅病历以了解初步诊断、治疗方案、感染的临床表现及结局。

结果

患者1在心脏移植后不久出现了临床上无法解释的败血症综合征;通过外周血涂片检查诊断出弓形虫寄生虫血症。尸检证实了诊断。患者2是一名正在接受淋巴瘤诱导化疗的儿童,出现了快速进展的神经功能恶化并伴有斑丘疹样皮疹;当组织学检查与免疫组化相结合时,回顾性诊断为弓形虫脂膜炎。两例患者的尸检均证实感染广泛播散。

结论

对于患有培养阴性败血症综合征的免疫功能低下患者,尤其是伴有神经、呼吸或不明原因皮肤病变的患者,鉴别诊断时应考虑播散性弓形虫病。对瑞氏染色的外周血涂片进行检查或对皮肤活检进行抗弓形虫免疫过氧化物酶研究可能具有诊断价值,并能迅速启动抗生素治疗。尸检结果对我们的两个病例均有帮助,记录了广泛存在的大量寄生虫负荷,并显示出众多具有诊断意义的弓形虫囊肿形式。

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