An invasive and diffuse cranial actinomycosis with a dura-based mass mimicking a brain tumor: illustrative case.

Dejen T Gebrewahd, Tsegazeab Laeke, Eyob Z Wendimagegnehu, Mestet Y Shiferaw, Tesfaye G Tefera, Ilili A Aliye, Taye J Robele, Bereket H Mekuria, Anteneh E Berga, Surafael M Mendere, Sebboona B Abelti
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Abstract

Background: Actinomycosis is a chronic suppurative infection caused by non-spore-forming, anaerobic, and filamentous gram-positive bacteria. Primary central nervous system involvement is rare, with no specific clinical features, causing a clinical diagnostic dilemma. Imaging can help in localizing and characterizing the lesion; however, a definitive diagnosis relies on culture and/or histopathology.

Observations: The authors describe a 29-year-old male farmer with a rare case of invasive and diffuse cranial actinomycosis with a dura-based mass mimicking a brain tumor. Brain magnetic resonance imaging showed a moderately enhanced right frontoparietal infiltrative dura-based mass with marked thickening of the skull and multiple scalp actinomycotic abscesses. He underwent microsurgical excision of the mass, orbital decompression, and debridement of the scalp abscess. Histopathology confirmed actinomycosis, and his postoperative course was uneventful.

Lessons: Invasive and diffuse cranial actinomycosis with a dura-based actinomycetoma is a rare presentation that poses a diagnostic challenge due to its nonspecific manifestations. Imaging is helpful in localizing and characterizing the lesion; however, histopathology remains the gold standard for diagnosing actinomycosis. A high index of suspicion is also warranted in patients with predisposing factors to promote an early diagnosis and the initiation of appropriate treatments to improve functional recovery and limit residual deficits. https://thejns.org/doi/10.3171/CASE24210.

侵袭性弥漫性颅骨放线菌病,硬脑膜肿块模仿脑肿瘤:示例病例。
背景:放线菌病是一种慢性化脓性感染,由非芽孢杆菌、厌氧菌和丝状革兰氏阳性菌引起。原发性中枢神经系统受累非常罕见,没有特殊的临床特征,造成临床诊断上的难题。影像学检查有助于确定病灶的位置和特征,但明确诊断还需依靠培养和/或组织病理学检查:作者描述了一名 29 岁男性农民的罕见病例,他患有侵袭性和弥漫性颅骨放线菌病,硬脑膜肿块模仿脑肿瘤。脑磁共振成像显示,右侧额顶浸润性硬脑膜肿块中度增强,颅骨明显增厚,头皮多处放线菌脓肿。他接受了显微手术切除肿块、眼眶减压和头皮脓肿清创。组织病理证实为放线菌病,术后恢复顺利:启示:伴有硬脑膜放线菌瘤的侵袭性和弥漫性颅骨放线菌病是一种罕见的病症,由于其无特异性表现,给诊断带来了挑战。影像学检查有助于确定病变的位置和特征;然而,组织病理学仍是诊断放线菌病的金标准。https://thejns.org/doi/10.3171/CASE24210。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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