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表现为肺尖肿块和霍纳综合征的T1神经根神经瘤。

T1-nerve root neuroma presenting with apical mass and Horner's syndrome.

作者信息

Bosnjak Roman, Bacovnik Urska, Podnar Simon, Benedicic Mitja

机构信息

Department of Neurosurgery, Division of Surgery, University Medical Center, Ljubljana, Slovenia.

出版信息

J Brachial Plex Peripher Nerve Inj. 2007 Mar 19;2:7. doi: 10.1186/1749-7221-2-7.

Abstract

BACKGROUND

The appearance of dumbbell neuroma of the first thoracic root is extremely rare. The extradural component of a T1-dumbbell neuroma may present as an apical mass. The diagnosis of hand weakness is complex and may be delayed in T1-neuroma because of absence of the palpable cervical mass. One-stage removal of a T1-root neuroma and its intrathoracic extension demanded an extended posterior midline approach in the sitting position.

CASE PRESENTATION

A 51-year old man had suffered a traumatic partial tendon rupture of his wrist flexor muscles 6 years ago. Since the incident he occasionally felt fullness and tenderness in the affected forearm with some tingling in his fingers bilaterally. During the last two years the hand weakness was continuous and hypotrophy of the medial flexor and intrinsic hand muscles had become apparent. Electrophysiological studies revealed an ulnar neuropathy in addition to mild median and radial nerve dysfunction, including a mild contralateral carpal tunnel syndrome. The diagnostic work-up for multiple mononeuropathy in the upper extremity was negative. Repeated electrophysiological studies revealed fibrillations in the C7 paravertebral muscles on the affected side. Chest x-ray revealed a large round apical mass on the affected side. A Horner's syndrome was noted at this point of diagnostic work-up. MRI of the cervical and thoracic spine revealed a dumbbell T1 neuroma enlarging the intervertebral foramen at T1-2 and a 5 cm large extradural tumor with extension into the apex of the ipsilateral lung. The patient underwent surgery in sitting position using a left dorsal midline approach. Although the T1 root could not be preserved, the patient's neurological condition was unchanged after the surgery.

CONCLUSION

Extended posterior midline exposure described here using hemilaminectomy, unilateral facetectomy and costo-transversectomy is efficient and safe for one-stage removal of dumbbell tumors at the T1 level with a predominantly extraforaminal component in the apex of the lung extending up to 6-7 cm laterally. Horner's syndrome, if present and observed, may significantly narrow the differential diagnosis of hand weakness caused by T1-root tumors.

摘要

背景

第一胸神经根哑铃形神经瘤极为罕见。T1 哑铃形神经瘤的硬膜外部分可表现为肺尖肿块。手部无力的诊断较为复杂,在 T1 神经瘤中可能因未触及颈部肿块而延迟诊断。一期切除 T1 神经根神经瘤及其胸内延伸部分需要在坐位采用扩大的后正中入路。

病例介绍

一名 51 岁男性 6 年前腕部屈肌肌腱发生创伤性部分断裂。自该事件后,他偶尔感到患侧前臂饱满和压痛,双侧手指有一些刺痛感。在过去两年中,手部无力持续存在,内侧屈肌和手部固有肌萎缩明显。电生理研究显示除轻度正中神经和桡神经功能障碍外,还有尺神经病变,包括轻度对侧腕管综合征。上肢多发性单神经病的诊断检查结果为阴性。重复电生理研究显示患侧 C7 椎旁肌有纤颤。胸部 X 光显示患侧有一个大的圆形肺尖肿块。在诊断检查的这一阶段发现了霍纳综合征。颈椎和胸椎的 MRI 显示一个哑铃形 T1 神经瘤使 T1-2 椎间孔扩大,还有一个 5 厘米大的硬膜外肿瘤延伸至同侧肺尖。患者采用左侧后正中入路在坐位接受手术。尽管未能保留 T1 神经根,但术后患者的神经状况未变。

结论

本文所述的采用半椎板切除术、单侧关节突切除术和肋横突切除术的扩大后正中暴露法,对于一期切除 T1 水平以肺尖为主的哑铃形肿瘤且其椎间孔外成分向外侧延伸达 6 - 7 厘米是有效且安全的。如果存在并观察到霍纳综合征,可能会显著缩小由 T1 神经根肿瘤引起的手部无力的鉴别诊断范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b43/1831774/f9a7c2293d2b/1749-7221-2-7-1.jpg

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