Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India.
Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India.
World Neurosurg. 2018 Jul;115:e349-e359. doi: 10.1016/j.wneu.2018.04.056. Epub 2018 Apr 17.
To describe clinical characteristics of patients with intracranial cryptococcoma, clinicopathologic findings, and outcomes after surgery.
Clinical data were collected from hospital case records, and pathologic confirmation was done by a neuropathologist. Clinical details, imaging features, and treatment modalities were evaluated and correlated with outcomes based on regular follow-up.
This case series included 5 cases of histology- and culture-proven intracranial cryptococcoma. Three patients (60%) were aged between the 3rd and 5th decades. Three cases were supratentorial in location, and 2 were in the posterior fossa. One patient presented with seizures. Three patients (60%) presented with fever. Three patients (60%) had papilledema, and 4 (80%) had signs of meningeal irritation. Four patients (80%) were immunocompetent. Only 1 patient was immunocompromised. All lesions were peripherally enhancing on computed tomography. Four of 5 patients underwent surgical decompression without any residue. Only 1 patient underwent stereotactic biopsy. All patients received antifungal therapy. One patient who was immunocompromised developed multiorgan failure and died after 2 months after surgery (20%). Of 5 cases, 4 (80%) had a good outcome with a mean follow-up of 5 years.
Cryptococcus gattii is a rarer species implicated in intracranial cryptococcoma that is seen along with the more common Cryptococcus neoformans. Early diagnosis and surgical decompression followed by intravenous amphotericin B therapy for at least 6 weeks and concomitant therapy with fluconazole for prolonged periods may reduce morbidity and mortality.
描述颅内隐球菌肿患者的临床特征、临床病理发现以及手术后的结局。
从医院病历中收集临床数据,并由神经病理学家进行病理确认。评估临床细节、影像学特征和治疗方式,并根据定期随访将其与结局相关联。
本病例系列包括 5 例经组织学和培养证实的颅内隐球菌肿。3 名患者(60%)年龄在 30 至 50 岁之间。3 例位于幕上,2 例位于后颅窝。1 例患者出现癫痫发作。3 例患者(60%)发热。3 例患者(60%)出现视乳头水肿,4 例(80%)有脑膜刺激征。4 名患者(80%)免疫功能正常,仅有 1 名患者免疫功能低下。所有病变在 CT 上均呈周边增强。5 例患者中有 4 例(80%)接受了手术减压,无任何残留。仅有 1 例患者接受了立体定向活检。所有患者均接受了抗真菌治疗。1 名免疫功能低下的患者在手术后 2 个月因多器官衰竭而死亡(20%)。5 例患者中,4 例(80%)有良好的结局,平均随访 5 年。
新型隐球菌是一种较少见的种属,与更为常见的新型隐球菌一起引起颅内隐球菌肿。早期诊断和手术减压,随后静脉注射两性霉素 B 治疗至少 6 周,并同时长期应用氟康唑治疗,可能会降低发病率和死亡率。