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神经轴的多发性钙化性假瘤

Multiple Calcifying Pseudoneoplasms of the Neuraxis.

作者信息

Brasiliense Leonardo B, Dickson Dennis W, Nakhleh Raouf E, Tawk Rabih G, Wharen Robert

机构信息

Neurosurgery, Division of Neurosurgery, University of Arizona, Tucson, AZ.

Pathology, Mayo Clinic, Jacksonville, FL.

出版信息

Cureus. 2017 Feb 21;9(2):e1044. doi: 10.7759/cureus.1044.

Abstract

Calcifying pseudoneoplasms of the neuraxis (CAPNONs) are extremely rare tumors that are frequently misdiagnosed and overlooked by clinicians. To date, only 40 intracranial lesions have been reported, and in all instances, they were found as a solitary calcified mass. To our knowledge, the current case report is the first to illustrate the development of multiple intraaxial CAPNONs and shed more light on the origin of these lesions. We discuss the case of a 67-year-old woman who presented with a six-year history of recurrent seizures. Magnetic resonance imaging revealed two similar heterogeneous intracranial masses in the ventral midbrain and left frontal white matter with indications of more aggressive behavior in the supratentorial tumor. The lesion was resected, and histopathological analysis showed tissue containing nodules of chondromyxoid material with a coarsely fibrillar matrix and focal alveolar pattern. Palisading cells were noted around the edges as well as dystrophic calcifications and osseous metaplasia, consistent with CAPNON. Interestingly, the patient had a previous history of multiple brain abscesses and a mycotic aneurysm. At her four-month follow-up visit, the patient remained seizure-free and there were no indications of residual tumor or recurrence. In contrast to previous reports, intracranial CAPNONs may manifest as multiple lesions and clinicians should include these tumors in the differential diagnosis of intra-axial calcified masses. The previous history of brain abscesses raises the suspicion of an abnormal proliferative process following an insult to the brain tissue as the underlying origin of these lesions.

摘要

神经轴钙化性假瘤(CAPNONs)是极为罕见的肿瘤,临床医生常对其误诊和漏诊。迄今为止,仅报道过40例颅内病变,且所有病例均为单个钙化肿块。据我们所知,本病例报告首次阐述了多发轴内CAPNONs的发生情况,并进一步揭示了这些病变的起源。我们讨论了一名67岁女性患者的病例,该患者有6年的癫痫复发史。磁共振成像显示,在中脑腹侧和左侧额叶白质有两个类似的异质性颅内肿块,幕上肿瘤表现出更具侵袭性的特征。病变被切除,组织病理学分析显示,组织中含有软骨黏液样物质结节,伴有粗糙的纤维状基质和局灶性肺泡样结构。在边缘可见栅栏状细胞以及营养不良性钙化和骨化生,符合CAPNON的表现。有趣的是,该患者既往有多发脑脓肿和真菌性动脉瘤病史。在4个月的随访中,患者无癫痫发作,也没有残留肿瘤或复发的迹象。与既往报道不同,颅内CAPNONs可能表现为多发病变,临床医生应将这些肿瘤纳入轴内钙化肿块的鉴别诊断中。既往脑脓肿病史提示,脑组织受损后的异常增殖过程可能是这些病变的潜在起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2875/5360384/d8f013f62563/cureus-0009-00000001044-i01.jpg

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