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牙源性颅内放线菌病伪装成自身免疫性眼眶肌炎:1 例致死病例及文献复习。

Intracranial actinomycosis of odontogenic origin masquerading as auto-immune orbital myositis: a fatal case and review of the literature.

机构信息

Department of Ophthalmology, Erasmus Medical Center, Rotterdam, The Netherlands.

Department of Orbital Oculoplastic and Lacrimal Surgery, The Rotterdam Eye Hospital, PO box 70030, 3000 LM, Rotterdam, The Netherlands.

出版信息

BMC Infect Dis. 2019 Sep 2;19(1):763. doi: 10.1186/s12879-019-4408-2.

Abstract

BACKGROUND

Actinomycetes can rarely cause intracranial infection and may cause a variety of complications. We describe a fatal case of intracranial and intra-orbital actinomycosis of odontogenic origin with a unique presentation and route of dissemination. Also, we provide a review of the current literature.

CASE PRESENTATION

A 58-year-old man presented with diplopia and progressive pain behind his left eye. Six weeks earlier he had undergone a dental extraction, followed by clindamycin treatment for a presumed maxillary infection. The diplopia responded to steroids but recurred after cessation. The diplopia was thought to result from myositis of the left medial rectus muscle, possibly related to a defect in the lamina papyracea. During exploration there was no abnormal tissue for biopsy. The medial wall was reconstructed and the myositis responded again to steroids. Within weeks a myositis on the right side occurred, with CT evidence of muscle swelling. Several months later he presented with right hemiparesis and dysarthria. Despite treatment the patient deteriorated, developed extensive intracranial hemorrhage, and died. Autopsy showed bacterial aggregates suggestive of actinomycotic meningoencephalitis with septic thromboembolism. Retrospectively, imaging studies showed abnormalities in the left infratemporal fossa and skull base and bilateral cavernous sinus.

CONCLUSIONS

In conclusion, intracranial actinomycosis is difficult to diagnose, with potentially fatal outcome. An accurate diagnosis can often only be established by means of histology and biopsy should be performed whenever feasible. This is the first report of actinomycotic orbital involvement of odontogenic origin, presenting initially as bilateral orbital myositis rather than as orbital abscess. Infection from the upper left jaw extended to the left infratemporal fossa, skull base and meninges and subsequently to the cavernous sinus and the orbits.

摘要

背景

放线菌很少引起颅内感染,可引起多种并发症。我们描述了一例由牙源性来源引起的具有独特表现和播散途径的致命性颅内和眶内放线菌病。同时,我们对当前文献进行了回顾。

病例介绍

一名 58 岁男性因左眼复视和左眼后疼痛进行性加重就诊。六周前,他接受了一次拔牙手术,随后因疑似上颌感染接受克林霉素治疗。使用类固醇治疗后复视得到缓解,但停药后又复发。复视被认为是由于左眼内直肌肌炎引起的,可能与纸板缺陷有关。在探查过程中没有发现异常组织进行活检。重建了内侧壁,肌炎再次对类固醇治疗有反应。几周后,右侧出现肌炎,CT 显示肌肉肿胀。几个月后,他出现右侧偏瘫和构音障碍。尽管进行了治疗,患者仍病情恶化,出现广泛的颅内出血,最终死亡。尸检显示有细菌聚集体,提示为放线菌性脑膜脑炎伴败血症性血栓栓塞。回顾性影像学研究显示左侧颞下窝和颅底以及双侧海绵窦异常。

结论

总之,颅内放线菌病难以诊断,可能导致致命后果。准确的诊断通常只能通过组织学来确定,只要可行,应进行活检。这是首例由牙源性来源引起的放线菌性眶内感染的报道,最初表现为双侧眶肌炎,而不是眶脓肿。左上颚的感染延伸至左侧颞下窝、颅底和脑膜,随后蔓延至海绵窦和眼眶。

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