颅内古神经分裂瘤的临床和放射学特征:单一机构的回顾性分析

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Takahiro Tsuchiya, Masako Ikemura, Satoru Miyawaki, Yu Teranishi, Kenta Ohara, Tetsuo Ushiku, Nobuhito Saito
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引用次数: 0

摘要

古分裂瘤(AS)是分裂瘤的一种亚型,其特点是尽管病理发生了退行性变化,但病情发展缓慢。虽然它被认为是一种良性肿瘤,但之前的大多数报道都集中于颅外的古分裂瘤,因此颅内古分裂瘤的临床特征尚不明确。我们纳入了 174 例因散发性颅内分裂瘤接受手术的患者,其中 13 例患者(7.5%)被确诊为 AS。强直性脊柱炎患者的囊肿发生率(92.3% vs. 44.7%,p <0.001)、出血(38.5% vs. 6.9%,p = 0.003)和钙化(15.4% vs. 1.3%,p = 0.029)明显高于传统的分裂瘤。强直性脊柱炎患者的肿瘤最大直径也更大(35 毫米对 29 毫米,p = 0.017)。从症状出现到手术的中位持续时间(7.0 个月 vs. 12.5 个月,p = 0.740)和术后复发的概率(p = 0.949)在组间没有显著差异。颅内强直性脊柱炎与囊肿形成密切相关,临床过程良性,复发率较低,需要进行挽救治疗。据报道,颅外强直性脊柱炎的特点是在长期临床过程中进展缓慢,而在我们的研究中,颅内强直性脊柱炎的进展并不缓慢,并且表现出与颅外强直性脊柱炎不同的临床特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and radiological features of intracranial ancient schwannomas: a single-institution, retrospective analysis

Ancient schwannoma (AS) is a subtype of schwannoma characterized by slow progression despite degenerative changes in pathology. Although it is considered a benign tumor, most previous reports have focused on extracranial AS; therefore, the clinical characteristics of intracranial AS is not clear. We included 174 patients who underwent surgery for sporadic intracranial schwannoma, and 13 patients (7.5%) were diagnosed with AS. Cysts were significantly more common in patients with AS than conventional schwannomas (92.3% vs. 44.7%, p < 0.001), as was bleeding (38.5% vs. 6.9%, p = 0.003) and calcification (15.4% vs. 1.3%, p = 0.029). The maximum tumor diameter was also larger in patients with AS (35 mm vs. 29 mm, p = 0.017). The median duration from symptom onset to surgery (7.0 vs. 12.5 months, p = 0.740) did not significantly differ between groups, nor did the probability of postoperative recurrence (p = 0.949). Intracranial AS was strongly associated with cyst formation and exhibited a benign clinical course with a lower rate of recurrence and need for salvage treatment. Extracranial AS is reportedly characterized by a slow progression through a long-term clinical course, whereas intracranial AS did not progress slowly in our study and exhibited different clinical features to those reported for extracranial AS.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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