Rare Case Of Plasma Cell Hyperplasia (Inflammatory Pseudotumor) Of The Central Nervous System

R. Azad, S. Azad, S. Kudesia, P. Arora
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引用次数: 1

Abstract

We report a rare case of Plasma cell hyperplasia (PCH) of the Central Nervous System (CNS) in a 25 year old male involving the pachymeninges and brain parenchyma which was a diagnostic dilemma due to overlapping imaging features with other pathologies. On CT, there was white matter edema and gyral swelling in left parietoccipital region. The involved region showed ill-defined diffuse sheet like peripheral enhancement on post contrast CT, which was thought to be intraparencymal than pachymeningeal. On post contrast MR imaging, there was thick sheet like pachymeningeal enhancement with dural tail formation in addition to diffuse peripheral gyral enhancement and white matter edema in above location. Gross total excision of dural based lesion was done and histopathology revealed features of plasma cell hyperplasia. No evidence of recurrence was seen at six month follow-up.
中枢神经系统浆细胞增生(炎性假瘤)一例
我们报告一例罕见的25岁男性中枢神经系统浆细胞增生(PCH),累及厚脑膜和脑实质,由于与其他病理重叠的影像特征,这是一个诊断困境。CT表现为左侧顶骨白质水肿及脑回肿胀。受累区域在CT上显示模糊的弥漫性片状周围增强,认为是透明细胞内而不是厚脑膜。磁共振造影后可见厚片状厚脑膜增强,伴硬脑膜尾形成,弥漫性外周脑回增强及以上部位白质水肿。硬脑膜基底病变大体切除,组织病理学显示浆细胞增生。随访6个月无复发迹象。
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