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免疫功能低下宿主的中枢神经系统感染:一种诊断方法。

Central nervous system infections in the compromised host: a diagnostic approach.

作者信息

Cunha B A

机构信息

State University of New York School of Medicine, Stony Brook, New York, USA.

出版信息

Infect Dis Clin North Am. 2001 Jun;15(2):567-90. doi: 10.1016/s0891-5520(05)70160-4.

Abstract

The diagnostic approach to the compromised host with CNS infection depends on an analysis of the patient's clinical manifestations of CNS disease, the acuteness or subacuteness of the clinical presentation, and an analysis of the type of immune defect compromising the patient's host defenses. Most patients with CNS infections may be grouped into those with meningeal signs, or those with mass lesions. Other common manifestations of CNS infection include encephalopathy, seizures, or a stroke-like presentation. Most pathogens have a predictable clinical presentation that differs from that of the normal host. CNS Aspergillus infections present either as mass lesions (e.g., brain abscess), or as cerebral infarcts, but rarely as meningitis. Cryptococcus neoformans, in contrast, usually presents as a meningitis but not as a cerebral mass lesion even when cryptococcal elements are present. Aspergillus and Cryptococcus CNS infections are manifestations of impaired host defenses, and rarely occur in immunocompetent hosts. In contrast, the clinical presentation of Nocardia infections in the CNS is the same in normal and compromised hosts, although more frequent in compromised hosts. The acuteness of the clinical presentation coupled with the CNS symptomatology further adds to limit differential diagnostic possibilities. Excluding stroke-like presentations, CNS mass lesions tend to present subacutely or chronically. Meningitis and encephalitis tend to present more acutely, which is of some assistance in limiting differential diagnostic possibilities. The analysis of the type of immune defect predicts the range of possible pathogens likely to be responsible for the patient's CNS signs and symptoms. Patients with diseases and disorders that decrease B-lymphocyte function are particularly susceptible to meningitis caused by encapsulated bacterial pathogens. The presentation of bacterial meningitis is essentially the same in normal and compromised hosts with impaired B-lymphocyte immunity. Compromised hosts with impaired T-lymphocyte or macrophage function are prone to develop CNS infections caused by intracellular pathogens. The most common intracellular pathogens are the fungi, particularly Aspergillus, other bacteria (e.g., Nocardia), viruses (i.e., HSV, JC, CMV, HHV-6), and parasites (e.g., T. gondii). The clinical syndromic approach is most accurate when combining the rapidity of clinical presentation and the expression of CNS infection with the defect in host defenses. The presence of extra-CNS sites of involvement also may be helpful in the diagnosis. A patient with impaired cellular immunity with mass lesions in the lungs and brain that have appeared subacutely or chronically should suggest Nocardia or Aspergillus rather than cryptococcosis or toxoplasmosis. Patients with T-lymphocyte defects presenting with meningitis generally have meningitis caused by Listeria or Cryptococcus rather than toxoplasmosis or CMV infection. The disorders that impair host defenses, and the therapeutic modalities used to treat these disorders, may have CNS manifestations that mimic infections of the CNS clinically. Clinicians must be ever vigilant to rule out the mimics of CNS infections caused by noninfectious etiologies. Although the syndromic approach is useful in limiting diagnostic possibilities, a specific diagnosis still is essential in compromised hosts in order to describe effective therapy. Bacterial meningitis, cryptococcal meningitis, and tuberculosis easily are diagnosed accurately from stain, culture, or serology of the CSF. In contrast, patients with CNS mass lesions usually require a tissue biopsy to arrive at a specific etiologic diagnosis. In a compromised host with impaired cellular immunity in which the differential diagnosis of a CNS mass lesion is between TB, lymphoma, and toxoplasmosis, a trial of empiric therapy is warranted. Antitoxoplasmosis therapy may be initiated empirically and usually results in clinical improvement after 2 to 3 weeks of therapy. The nonresponse to antitoxoplasmosis therapy in such a patient would warrant an empiric trial of antituberculous therapy. Lack of response to anti-Toxoplasma and antituberculous therapy should suggest a noninfectious etiology (e.g., CNS lymphoma). Fortunately, most infections in compromised hosts are similar in their clinical presentation to those in the normal host, particularly in the case of meningitis. The compromised host is different than the normal host in the distribution of pathogens, which is determined by the nature of the host defense defect. In compromised hosts, differential diagnostic possibilities are more extensive and the likelihood of noninfectious explanations for CNS symptomatology is greater. (ABSTRACT TRUNCATED)

摘要

对于患有中枢神经系统感染的免疫功能低下宿主,其诊断方法取决于对患者中枢神经系统疾病临床表现、临床表现的急性或亚急性程度的分析,以及对损害患者宿主防御功能的免疫缺陷类型的分析。大多数患有中枢神经系统感染的患者可分为有脑膜刺激征的患者或有占位性病变的患者。中枢神经系统感染的其他常见表现包括脑病、癫痫发作或类似中风的表现。大多数病原体具有可预测的临床表现,与正常宿主不同。中枢神经系统曲霉菌感染可表现为占位性病变(如脑脓肿)或脑梗死,但很少表现为脑膜炎。相比之下,新型隐球菌通常表现为脑膜炎,即使存在隐球菌成分,也不会表现为脑占位性病变。曲霉菌和隐球菌中枢神经系统感染是宿主防御功能受损的表现,很少发生在免疫功能正常的宿主中。相比之下,诺卡菌中枢神经系统感染在正常宿主和免疫功能低下宿主中的临床表现相同,尽管在免疫功能低下宿主中更常见。临床表现的急性程度加上中枢神经系统症状进一步限制了鉴别诊断的可能性。排除类似中风的表现,中枢神经系统占位性病变往往呈亚急性或慢性表现。脑膜炎和脑炎往往表现得更急性,这在一定程度上有助于限制鉴别诊断的可能性。对免疫缺陷类型的分析可预测可能导致患者中枢神经系统体征和症状的病原体范围。患有导致B淋巴细胞功能下降的疾病和病症的患者特别容易感染由包膜细菌病原体引起的脑膜炎。在B淋巴细胞免疫受损的正常宿主和免疫功能低下宿主中,细菌性脑膜炎的表现基本相同。T淋巴细胞或巨噬细胞功能受损的免疫功能低下宿主容易发生由细胞内病原体引起的中枢神经系统感染。最常见的细胞内病原体是真菌,尤其是曲霉菌,其他细菌(如诺卡菌)、病毒(即单纯疱疹病毒、JC病毒、巨细胞病毒、人疱疹病毒6型)和寄生虫(如弓形虫)。当结合临床表现的快速性、中枢神经系统感染的表现以及宿主防御缺陷时,临床综合征方法最为准确。存在中枢神经系统外的受累部位也可能有助于诊断。一名细胞免疫受损的患者,肺部和脑部出现亚急性或慢性占位性病变,应提示为诺卡菌或曲霉菌感染,而非隐球菌病或弓形虫病。表现为脑膜炎的T淋巴细胞缺陷患者通常患有由李斯特菌或隐球菌引起的脑膜炎,而非弓形虫病或巨细胞病毒感染。损害宿主防御功能的疾病以及用于治疗这些疾病的治疗方式可能具有临床上类似于中枢神经系统感染的中枢神经系统表现。临床医生必须始终保持警惕,以排除由非感染性病因引起的中枢神经系统感染的模仿情况。尽管综合征方法有助于限制诊断可能性,但对于免疫功能低下宿主,明确诊断仍然至关重要,以便描述有效的治疗方法。细菌性脑膜炎、隐球菌性脑膜炎和结核病很容易通过脑脊液的涂片、培养或血清学检查准确诊断。相比之下,患有中枢神经系统占位性病变的患者通常需要进行组织活检以得出具体病因诊断。在一名细胞免疫受损的免疫功能低下宿主中,中枢神经系统占位性病变的鉴别诊断在结核病、淋巴瘤和弓形虫病之间,进行经验性治疗试验是必要的。可以经验性地开始抗弓形虫病治疗,通常在治疗2至3周后临床症状会改善。在这样的患者中,对抗弓形虫病治疗无反应则需要进行抗结核治疗的经验性试验。对抗弓形虫病和抗结核治疗均无反应应提示为非感染性病因(如中枢神经系统淋巴瘤)。幸运的是,免疫功能低下宿主中的大多数感染在临床表现上与正常宿主相似,尤其是在脑膜炎的情况下。免疫功能低下宿主与正常宿主的不同之处在于病原体的分布,这由宿主防御缺陷 的性质决定。在免疫功能低下宿主中,鉴别诊断的可能性更广泛且中枢神经系统症状的非感染性解释的可能性更大。(摘要截断)

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