Department of Radiodiagnosis, Neuroimaging & Interventional Neuroradiology Division, 29751PGIMER, Chandigarh, India.
Departmentof Pathology 80369IGMC, Shimla, India.
Neuroradiol J. 2023 Feb;36(1):59-67. doi: 10.1177/19714009221098372. Epub 2022 May 10.
Neurocysticercosis, the commonest neuro-parasite, sometimes presents as complex ring enhancing lesion causing diagnostic dilemma. We aim to establish radio-histo-morphological equivalents of early events in degeneration of the parasite to explain such imaging phenotypes.
We compared patterns of degeneration in 23 randomly selected complex NCC on MRI with histo-morphology in 30 cysts obtained from an unrelated post mortem brain.
The anatomy of the parasite and the degenerative patterns of the scolex (hydropic changes, calcification, evagination, and fragmentation) and the cyst wall (undulation, accessory loculi, and frank disruption) were well demonstrated on both. The intact scolex remarkably resembled head of intestinal Taenia. The complex lesions were conglomeration of multiple communicating cysts with a single parent cyst and multiple daughter cysts. The parent cysts contained a solitary variably degenerated scolex, had thicker walls and associated chronic inflammation. The remaining cysts of the lesion complex contained no scolex, had poorly organized walls, turbid contents, and florid perilesional enhancement with leakage of contrast. Three lesions assumed a multi-cystic pseudo-tumorous pattern, of which two resolved into solitary calcific remnants on follow up.
Complex lesion in NCC result from degeneration of solitary parasite with perilesional gliosis, surrounded by multiple non-larval daughter cysts inciting acute intra and perilesional inflammation due to enhanced antigenic challenge. Possibly, attempted abortive asexual reproduction by the cellulose cyst as a preterminal event results in a "limited Racemose like transition." Correct interpretation has diagnostic and therapeutic implications as active lesions and their fibrocalcific residue may have greater epileptogenic potential.
神经囊虫病是最常见的神经寄生虫病,有时表现为复杂的环形增强病变,导致诊断困难。我们旨在确定寄生虫退变早期事件的放射组织形态学等价物,以解释这种影像学表型。
我们比较了 23 例随机选择的复杂神经囊虫病 MRI 退变模式与 30 例来自无关死后大脑的囊肿的组织形态学。
寄生虫的解剖结构和头节的退变模式(水肿变化、钙化、外凸和碎裂)以及囊壁的退变模式(波动、附属小房和明显破裂)在两者中均得到很好的显示。完整的头节非常类似于肠绦虫的头部。复杂病变是由多个具有单个母囊和多个子囊的连通性囊肿聚集而成。母囊肿含有单个可变退变的头节,壁较厚,伴有慢性炎症。病变复杂的剩余囊肿中没有头节,囊壁组织排列较差,内容物混浊,周边强化明显,伴有对比剂渗漏。三个病变呈多囊肿假性肿瘤样模式,其中两个在随访中消退为单个钙化残余物。
神经囊虫病的复杂病变是由单个寄生虫退变引起的,周围有多个非幼虫子囊,由于抗原性挑战增加,引发周边胶质增生和急性囊内和周边炎症。纤维素囊可能试图进行失败的无性繁殖,作为终末期事件,导致“有限的 Racemose 样转化”。正确的解释具有诊断和治疗意义,因为活动性病变及其纤维钙化残余物可能具有更大的致痫潜能。