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少突胶质细胞瘤样细胞增殖与血管瘤样脉管系统的关联——巧合还是致病相关病变?

Association of oligodendroglioma-like cell proliferation and angiomatous vasculature--coincidence or pathogenetically related lesions?

作者信息

Tews D S, Bohl J E, Van Lindert E, Ringel K

机构信息

Division of Neuropathology, Johannes-Gutenberg-University, Mainz, Germany.

出版信息

Clin Neuropathol. 1998 Mar-Apr;17(2):69-72.

PMID:9561327
Abstract

We report a case of an oligodendroglioma associated with a cavernous angioma. The patient, a 20-year-old man with an 8-year history of epileptic seizures, presented an acute onset of headache, nausea, and vomiting. Computerized tomographic scan and angiogram revealed multiple vascular malformations in both hemispheres including a cystic hemorraghic lesion with a perifocal edema attributing to a mass effect. Repeated puncture of the cyst failed to give improvement of elevated intracranial pressure. At surgery, the cyst and the underlying lesion were excised and found to be oligodendrocyte-rich tissue with malformed vascular tissue. Final histological examination revealed an oligodendroglioma associated with a cavernous angioma. As concurrence of oligodendroglioma and vascular malformation is rare, this case raises a broad range of differential diagnoses such as reactive oligodendroglial gliosis due to a vascular malformation, unusual vascularity of an oligodendroglioma as well as other kinds of cerebral tumors or malformations. The diagnostic difficulties as well as the pathogenetic and pathological significance of the concurrence of an oligodendroglioma and cavernous angioma are discussed.

摘要

我们报告一例少突胶质细胞瘤合并海绵状血管瘤的病例。该患者为一名20岁男性,有8年癫痫发作病史,此次出现头痛、恶心和呕吐的急性发作。计算机断层扫描和血管造影显示双侧半球有多个血管畸形,包括一个伴有灶周水肿的囊性出血性病变,考虑为占位效应所致。反复穿刺囊肿未能改善颅内压升高的情况。手术中,切除了囊肿及下方病变,发现是富含少突胶质细胞的组织伴畸形血管组织。最终组织学检查显示为少突胶质细胞瘤合并海绵状血管瘤。由于少突胶质细胞瘤与血管畸形同时存在的情况罕见,该病例引发了广泛的鉴别诊断,如血管畸形导致的反应性少突胶质细胞胶质增生、少突胶质细胞瘤的异常血管形成以及其他类型的脑肿瘤或畸形。文中讨论了少突胶质细胞瘤与海绵状血管瘤同时存在的诊断困难以及其发病机制和病理意义。

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