Mogilner A, Jallo G I, Zagzag D, Kelly P J
Department of Neurosurgery, New York University Medical Center, New York 10016, USA.
Neurosurgery. 1998 Oct;43(4):949-52. doi: 10.1097/00006123-199810000-00130.
Cerebral Nocardia abscesses are rare, accounting for approximately 1 to 2% of all cerebral abscesses. Prompt aggressive surgical treatment involving craniotomy and excision of these lesions has been advocated by many authors, because these lesions have significantly higher morbidity and mortality rates than do most other cerebral abscesses. We report an atypical presentation of cerebral nocardiosis localized to the choroid plexus of the lateral ventricle.
A 56-year-old man presented with a 3-week history of fever, cough, and progressive headache and an ensuing 3-day history of progressive lethargy, confusion, and gait ataxia. Radiographic studies demonstrated a loculated contrast-enhancing left lateral ventricular lesion with significant perilesional parenchymal edema that was thought preoperatively to be a neoplasm.
The patient underwent a craniotomy for resection of the lesion. Intraoperatively, a reddish gray lesion with purulent exudate was encountered within the left lateral ventricle intimately adherent to the choroid plexus as well as to the ependyma and subependymal veins. A frozen section demonstrated an organizing abscess wall. The lesion was resected in its entirety, and multiple cultures were sent for analysis.
Microbiology cultures grew Nocardia asteroides. A course of intravenous antibiotics was started, which included trimethoprim-sulfamethoxazole, amikacin, and ceftriaxone. Two weeks after surgery, at the time of discharge, the patient's neurological status had improved considerably. Although Nocardia abscesses have been documented to occur throughout the central nervous system, the presentation of a lesion confined to the choroid plexus of the lateral ventricle with significant parenchymal edema is unusual and demonstrates that Nocardia abscesses must be considered in the differential diagnosis of a contrast-enhancing intraventricular mass lesion involving the choroid plexus.
脑诺卡菌脓肿较为罕见,约占所有脑脓肿的1%至2%。许多作者主张对这些病变进行积极的手术治疗,包括开颅手术和切除,因为与大多数其他脑脓肿相比,这些病变的发病率和死亡率显著更高。我们报告一例局限于侧脑室脉络丛的脑诺卡菌病的非典型表现。
一名56岁男性,有3周的发热、咳嗽及进行性头痛病史,随后3天出现进行性嗜睡、意识模糊和步态共济失调。影像学检查显示左侧侧脑室有一个有分隔的强化病变,病变周围实质有明显水肿,术前考虑为肿瘤。
患者接受开颅手术切除病变。术中,在左侧脑室内发现一个红灰色病变,伴有脓性渗出物,紧密附着于脉络丛、室管膜和室管膜下静脉。冰冻切片显示为一个正在机化的脓肿壁。病变被完整切除,并送多个培养物进行分析。
微生物培养结果为星形诺卡菌。开始静脉使用抗生素治疗,包括甲氧苄啶-磺胺甲恶唑、阿米卡星和头孢曲松。术后两周出院时,患者的神经状态有了显著改善。尽管诺卡菌脓肿已被证明可发生于整个中枢神经系统,但局限于侧脑室脉络丛且伴有明显实质水肿的病变表现并不常见,这表明在鉴别诊断涉及脉络丛的脑室内强化肿块病变时必须考虑诺卡菌脓肿。