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一名未确诊结节病患者的小脑隐球菌瘤:病例报告

Cerebellar cryptococcoma in a patient with undiagnosed sarcoidosis: case report.

作者信息

Kanaly Charles W, Selznick Lee A, Cummings Thomas J, Adamson D Cory

机构信息

Department of Surgery, Division of Neurosurgery, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Neurosurgery. 2007 Mar;60(3):E571; discussion E571. doi: 10.1227/01.NEU.0000255338.18404.C1.

DOI:10.1227/01.NEU.0000255338.18404.C1
PMID:17327765
Abstract

OBJECTIVE

We describe a patient with undiagnosed sarcoidosis who presented with a rare isolated cerebellar cryptococcoma masquerading as a metastatic brain tumor.

CLINICAL PRESENTATION

A 58-year-old man with a history of resected squamous cell carcinoma of the larynx and pulmonary nodules was found to have a left cerebellar lesion on neuroimaging after presenting with a 4-month history of occipital headaches. Neuroimaging revealed a large, lobulated, intra-axial, left cerebellar hemispheric mass with peripheral nodular enhancement, mild adjacent edema, and dense focal areas of calcification.

INTERVENTION

The patient underwent a left suboccipital craniotomy for gross total resection of the left cerebellar mass. Pathological examination of the resected specimen demonstrated a cryptococcoma, which was confirmed with a positive cerebrospinal fluid cryptococcal antigen. Postoperative evaluation revealed pulmonary sarcoidosis.

CONCLUSION

Central nervous system cryptococcoma is a rare infection that may present in a patient with no known history of immunosuppression and no clinical signs of infection. Diagnostically, this can be difficult to distinguish from a brain tumor. Central nervous system cryptococcoma is an opportunistic infection that typically occurs in the presence of an immunosuppressed state. Sarcoidosis should be considered a predisposing factor because patients with this underlying disease have an increased susceptibility to this central nervous system fungal infection.

摘要

目的

我们描述了一名未确诊结节病的患者,其表现为罕见的孤立性小脑隐球菌瘤,伪装成脑转移瘤。

临床表现

一名58岁男性,有喉鳞状细胞癌切除史和肺结节史,在出现4个月枕部头痛后,神经影像学检查发现左小脑病变。神经影像学显示左小脑半球有一个大的、分叶状的轴内肿块,周边结节状强化,轻度邻近水肿,并有密集的局灶性钙化区。

干预措施

患者接受了左枕下开颅手术,以大体全切左小脑肿块。切除标本的病理检查显示为隐球菌瘤,脑脊液隐球菌抗原检测呈阳性,进一步证实了诊断。术后评估显示患有肺结节病。

结论

中枢神经系统隐球菌瘤是一种罕见的感染,可能出现在无已知免疫抑制病史且无感染临床体征的患者中。在诊断上,这可能难以与脑肿瘤区分开来。中枢神经系统隐球菌瘤是一种机会性感染,通常发生在免疫抑制状态下。结节病应被视为一个易感因素,因为患有这种基础疾病的患者对这种中枢神经系统真菌感染的易感性增加。

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