Extremely Rare Presentation of Pilonidal Sinus Disease in the Posterior Cranial Fossa of a 2-Year-Old Patient: A Case Report.

IF 0.6 Q4 CLINICAL NEUROLOGY
Journal of Neurological Surgery Reports Pub Date : 2025-07-11 eCollection Date: 2025-07-01 DOI:10.1055/a-2641-6301
Hamzeh Yacoub, Aya Aqel, Mohammed Adas, Qais Hjouj, Zaid Yacoub, Rita Yacoub, Hadi Dababseh
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引用次数: 0

Abstract

A 2-year-old female patient presented after experiencing a generalized tonic-clonic seizure accompanied by fever, followed by a loss of consciousness. She underwent an urgent right frontal external ventricular drain placement. Intraoperative cerebrospinal fluid analysis was negative for infectious patterns. MRI showed a predominantly cystic lesion in the midline posterior fossa, with a compressive mass effect. Subsequently, she underwent a suboccipital craniotomy for microscopic resection of a posterior cranial fossa lesion. Histopathology reported keratin flakes with severe active inflammation, and foreign body type giant cell reaction in scalp excision with free hair shafts through the inflammatory focus, consistent with pilonidal sinus. The patient was then discharged home in good health.

极为罕见的后颅窝毛毛窦疾病1例2岁患者。
一名2岁的女性患者在经历了全身性强直阵挛性发作并伴有发热后出现意识丧失。她接受了紧急右额部外脑室引流术。术中脑脊液分析感染模式阴性。MRI显示后窝中线主要为囊性病变,伴压缩肿块效应。随后,她接受了枕下开颅术,显微切除后颅窝病变。组织病理学报告角蛋白薄片伴严重活动性炎症,异物型巨细胞反应,头皮切除游离毛轴穿过炎症灶,与毛突窦一致。病人随后健康出院回家。
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