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一例孤立性脑毛霉菌病的惰性病例:一种不常见的表现。

An indolent case of isolated cerebral mucormycosis: an uncommon presentation.

作者信息

Montgomery David J, Goldstein Randi S, Douse Dontre' M, Tuitt Jerome, Sinnott Michael

机构信息

Mercer University School of Medicine, Georgia, USA.

Memorial Health University Medical Center, Department of Internal Medicine, Savannah, Georgia, USA.

出版信息

Access Microbiol. 2019 May 7;1(7):e000023. doi: 10.1099/acmi.0.000023. eCollection 2019.

Abstract

INTRODUCTION

This case is a presentation of isolated central nervous system (CNS) Mucormycosis in an immunocompetent patient. This case is unique in its demonstration of isolated CNS involvement while lacking clear evidence elucidating an entry point.

CASE PRESENTATION

The patient is a 36-year-old man without a pertinent past medical history, who initially presented with altered mental status and a 5-day history of progressively slurred speech. His social history is significant for intravenous drug use and outdoor pest control work. The patient's head computed tomography (CT) scan without contrast demonstrated the presence of possible bilateral infarcts or masses involving the basal ganglia and periventricular white matter. The patient then progressed to facial diplegia with new onset hemiplegia. High-dose steroids were initiated due to concern for neurosarcoidosis. A lumbar puncture was ordered due to minimal improvement and suggested an inflammatory process. A stereotactic brain biopsy was then performed, demonstrating non-caseating granulomatous inflammation with giant cells. Liposomal amphotericin B was added to cover possible fungal etiology. The pathology report was consistent with an isolated cerebral mucormycosis infection. The etiology remained elusive with clear paranasal sinuses and no cutaneous manifestations. Due to extensive gray matter involvement, the patient was not a candidate for surgery.

CONCLUSION

This is a report of mucormycosis in a seemingly immunocompetent patient with either isolated CNS involvement or disseminated mucormycosis without an identifiable source. Although this patient did have two risk factors including intravenous drug use and outdoor working history, his lack of peripheral involvement demonstrates an uncommon presentation.

摘要

引言

本病例展示了一名免疫功能正常患者发生的孤立性中枢神经系统(CNS)毛霉菌病。该病例的独特之处在于其仅表现为中枢神经系统受累,而缺乏明确的感染入口证据。

病例介绍

患者为一名36岁男性,既往无相关病史,最初表现为精神状态改变和进行性言语不清5天。其社会史显示有静脉吸毒和户外害虫防治工作经历。患者的头颅计算机断层扫描(CT)平扫显示双侧基底节区和脑室周围白质可能存在梗死灶或肿块。随后患者进展为面瘫伴新发偏瘫。由于担心神经结节病,开始使用大剂量类固醇。因症状改善不明显而行腰椎穿刺,提示存在炎症过程。随后进行了立体定向脑活检,显示为非干酪样肉芽肿性炎症伴巨细胞。加用脂质体两性霉素B以覆盖可能的真菌病因。病理报告与孤立性脑毛霉菌病感染一致。病因仍不明确,鼻窦清晰且无皮肤表现。由于灰质广泛受累,患者不适合手术。

结论

本文报告了一例看似免疫功能正常的患者发生的毛霉菌病,其表现为孤立性中枢神经系统受累或播散性毛霉菌病但无明确感染源。尽管该患者确实有静脉吸毒和户外工作史这两个危险因素,但其缺乏外周受累表现显示出一种不常见的情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/932d/7481736/cb534900866d/acmi-1-023-g001.jpg

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