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一名患有联合可变免疫缺陷患者的脑弓形虫病

Cerebral toxoplasmosis in a patient with combined variable immunodeficiency.

作者信息

Czech Torrey, Shah Parthav, Lee Gunnar, Watanabe Gina, Ogasawara Christian, Noh Thomas

机构信息

Department of Internal Medicine, University of Hawaii John A. Burns School of Medicine, Honolulu, Hawaii, United States.

Department of Neurological Surgery, John A. Burns School of Medicine, Honolulu, Hawaii, United States.

出版信息

Surg Neurol Int. 2022 Aug 12;13:354. doi: 10.25259/SNI_532_2022. eCollection 2022.

Abstract

BACKGROUND

Cerebral toxoplasmosis is an opportunistic infection in patients but has rarely been described in the setting of compromised humoral immunodeficiency. Prompt diagnosis and treatment of the infection is critical in the care of these patients. Medical management is the mainstay of treatment of the infection. There have been very few reports of surgical management of cerebral toxoplasmosis.

CASE DESCRIPTION

We describe the case of a 40-year-old male who presented with headache, memory deficits, weight loss, and left-sided weakness in the setting of a known but undiagnosed brain lesion identified 1 month prior. Imaging demonstrated a right basal ganglia lesion which was initially presumed to be malignancy. On further workup including a positive serum test and biopsy including polymerase chain reaction analysis, diagnosis was confirmed as toxoplasmosis. On further investigation, he was found to have deficiencies in immunoglobulins consistent with common variable immunodeficiency (CVID). The patient underwent craniotomy with surgical debulking as repeat imaging showed increased size of mass with new satellite lesions and worsening hydrocephalus.

CONCLUSION

Cerebral toxoplasmosis is an important differential to consider in cases of intracerebral lesions and should not necessarily be excluded in the absence of compromised cellular immunity. In cases where there is no immunocompromised state and malignancy cannot immediately be established, CVID should be considered as an etiology. Due to the subtlety of CVID diagnosis, careful attention should be paid to history taking and workup for CVID should be considered as soon as possible. Surgical removal of these lesions in conjunction with medications is an effective treatment option.

摘要

背景

脑弓形虫病是患者的一种机会性感染,但在体液免疫缺陷的情况下很少被描述。及时诊断和治疗这种感染对这些患者的护理至关重要。药物治疗是该感染治疗的主要手段。关于脑弓形虫病手术治疗的报道非常少。

病例描述

我们描述了一名40岁男性的病例,该患者在1个月前发现有一个已知但未确诊的脑病变,出现头痛、记忆缺陷、体重减轻和左侧肢体无力。影像学检查显示右侧基底节区病变,最初推测为恶性肿瘤。进一步检查包括血清检查阳性和活检(包括聚合酶链反应分析),确诊为弓形虫病。进一步调查发现,他存在与常见变异型免疫缺陷(CVID)一致的免疫球蛋白缺乏。由于重复影像学检查显示肿块大小增加,出现新的卫星病灶且脑积水加重,患者接受了开颅手术并进行肿瘤减容。

结论

脑弓形虫病是脑内病变病例中需要考虑的重要鉴别诊断,在没有细胞免疫受损的情况下不一定排除。在没有免疫功能低下状态且不能立即确诊为恶性肿瘤的情况下,应考虑CVID为病因。由于CVID诊断较为隐匿,应仔细询问病史,尽早考虑对CVID进行检查。手术切除这些病变并结合药物治疗是一种有效的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dfa/9479566/89b808db6472/SNI-13-354-g001.jpg

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