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颈椎硬膜内外丛状神经鞘瘤

Intra-extradural plexiform schwannoma of the cervical spine.

作者信息

Sakaura Hironobu, Ohshima Kazuya, Iwasaki Motoki, Yoshikawa Hideki

机构信息

Department of Orthopedic Surgery, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

Spine (Phila Pa 1976). 2007 Oct 1;32(21):E611-4. doi: 10.1097/BRS.0b013e31815583b4.

Abstract

STUDY DESIGN

Case report.

OBJECTIVE

To describe the clinical and radiographic features of an extremely rare case with intra-extradural plexiform schwannoma of the cervical spine.

SUMMARY OF BACKGROUND DATA

Plexiform schwannoma is a rare neurogenic tumor that predominantly occurs in the dermis and subcutis. Noncutaneous deep-seated lesions have rarely been described. No cases of intra-extradural plexiform schwannoma of the cervical spine have previously been reported.

METHODS

A 16-year-old boy presented with a 3-month history of left neck and shoulder angle pain, motor weakness of the left upper extremity, clumsiness of bilateral hands, and mild gait disturbance. Preoperative magnetic resonance imaging showed a multinodular inhomogeneous dumbbell-shaped tumor encroaching on the cord at C3-C4. T1-weighted imaging showed the tumor as inhomogeneous with slightly higher intensity than muscle. T2-weighted imaging demonstrated a multinodular inhomogeneous tumor with much higher intensity than muscle, and each nodule of the tumor displayed a peripheral rim of higher intensity and central relatively lower intensity.

RESULTS

Through hemi-laminectomy from C3-C4 and facetectomy of the left side of C3-C4, the intradural parts of the multinodular tumor were completely extirpated and extradural parts of the multinodular tumor were enucleated as much as possible. Gross examination of the tumor showed yellowish-white soft contents that were encapsulated and multilobulated. Histologic examination revealed benign schwannoma. After surgery, preoperative neurologic symptoms completely resolved.

CONCLUSION

To the best of our knowledge, this is the first reported case of intra-extradural plexiform schwannoma. Careful magnetic resonance imaging might be helpful in suggesting this rare plexiform schwannoma before surgery.

摘要

研究设计

病例报告。

目的

描述一例极为罕见的颈椎硬膜内外丛状神经鞘瘤的临床和影像学特征。

背景资料总结

丛状神经鞘瘤是一种罕见的神经源性肿瘤,主要发生于真皮和皮下组织。非皮肤深层病变鲜有报道。此前尚无颈椎硬膜内外丛状神经鞘瘤的病例报告。

方法

一名16岁男孩,有3个月的左颈和肩胛角疼痛、左上肢运动无力、双手笨拙及轻度步态障碍病史。术前磁共振成像显示一个多结节不均匀哑铃形肿瘤侵犯C3 - C4节段脊髓。T1加权成像显示肿瘤不均匀,强度略高于肌肉。T2加权成像显示一个多结节不均匀肿瘤,强度远高于肌肉,肿瘤的每个结节周边呈高强度,中央相对低强度。

结果

通过C3 - C4半椎板切除术及C3 - C4左侧关节突切除术,多结节肿瘤的硬膜内部分被完全切除,多结节肿瘤的硬膜外部分尽可能地摘除。肿瘤大体检查显示为黄白色软内容物,有包膜且呈多叶状。组织学检查显示为良性神经鞘瘤。术后,术前神经症状完全缓解。

结论

据我们所知,这是首例报道的颈椎硬膜内外丛状神经鞘瘤病例。术前仔细的磁共振成像可能有助于提示这种罕见的丛状神经鞘瘤。

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