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梅克尔腔神经轴复发性钙化假瘤,囊肿切除后囊肿延伸至小脑脑桥池:一例报告

Recurrent Calcifying Pseudoneoplasm of the Neuraxis in Meckel's Cave with Cyst Extending into the Cerebellopontine Cistern after Resection of the Cystic Component: A Case Report.

作者信息

Yamada Ryuta, Kobayashi Hiroki, Nomura Yuichi, Oka Naoki, Kokuzawa Jouji, Kaku Yasuhiko

机构信息

Department of Neurosurgery, Asahi University Hospital, Gifu, Japan.

出版信息

Asian J Neurosurg. 2025 Mar 25;20(3):605-609. doi: 10.1055/s-0045-1806859. eCollection 2025 Sep.

Abstract

Calcifying pseudoneoplasms of the neuraxis (CAPNON) are rare non-neoplastic calcified lesions that can occur throughout the entire neuraxis. Cranial nerves may be involved in skull base lesions. Surgical resection usually has a good prognosis, with only a few cases of recurrence reported in the relevant literature. We experienced a recurrent case of CAPNON in Meckel's cave extending to the cerebellopontine cistern with involvement of the trigeminal nerve after initial resection of the cystic part of the lesion. A 48-year-old man presented with a 4-year history of right-sided ptosis. Magnetic resonance imaging revealed a calcified lesion arising in Meckel's cave, with a cystic lesion extending to the cerebellopontine cistern. The cystic part of the lesion was excised during the initial surgery using the right lateral suboccipital approach. However, the cystic lesion regrew to its preoperative size within 23 months. The right extradural subtemporal approach was used to successfully remove both the calcified mass in the right Meckel cave and the cystic lesion extending to the right cerebellopontine cistern during the resection of the lesion. The patient's neurological symptoms resolved postoperatively. CAPNON was identified during the histopathological examination. This report describes a rare case of CAPNON in Meckel's cave with a unique clinical course. After the first operation, cystic lesions recurred in the cerebellopontine cistern, but they were successfully treated by a second operation.

摘要

神经轴钙化性假瘤(CAPNON)是一种罕见的非肿瘤性钙化病变,可发生于整个神经轴。颅底病变可能累及脑神经。手术切除通常预后良好,相关文献中仅报道了少数复发病例。我们遇到一例CAPNON复发病例,最初切除病变的囊性部分后,位于梅克尔腔并延伸至小脑脑桥池,累及三叉神经。一名48岁男性有4年右侧上睑下垂病史。磁共振成像显示梅克尔腔内有一钙化病变,并有一囊性病变延伸至小脑脑桥池。初次手术采用右侧枕下外侧入路切除病变的囊性部分。然而,囊性病变在23个月内又恢复到术前大小。再次手术采用右侧硬膜外颞下入路,成功切除了右侧梅克尔腔内的钙化肿块及延伸至右侧小脑脑桥池的囊性病变。患者术后神经症状消失。组织病理学检查确诊为CAPNON。本报告描述了一例发生于梅克尔腔的罕见CAPNON病例,具有独特的临床病程。首次手术后,小脑脑桥池出现囊性病变复发,但通过二次手术成功治愈。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f3b/12370357/f023899ec5a5/10-1055-s-0045-1806859-i24100043-1.jpg

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