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颈部淋巴结结核切除术后格里斯尔综合征的保守治疗方法:1例罕见病例报告

Conservative approach for treatment of Grisel's syndrome after resection of lympahadenitis tuberculosis of the neck: A rare case report.

作者信息

Tobing Singkat Dohar A L, Hendriarto Andra, Wikanjaya Rio

机构信息

Orthopaedic and Traumatology Department, Dr. Cipto Mangunkusumo Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.

Orthopaedic and Traumatology Department, Dr. Cipto Mangunkusumo Hospital, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.

出版信息

Int J Surg Case Rep. 2021 Nov;88:106452. doi: 10.1016/j.ijscr.2021.106452. Epub 2021 Oct 1.

Abstract

INTRODUCTION

Grisel's syndrome is a rare condition characterized by nontraumatic rotatory subluxation of the atlantoaxial joint, which was caused by previous inflammation around the head and neck. It is usually seen in children and signed as torticollis. There was no consensus for management, yet early diagnosis and treatment is paramount.

PRESENTATION OF CASE

A 5-year-old girl came to outpatient clinic complaining of wry neck 1 day after surgical excision of her TB lymphadenitis and got worsen by time. There was no history of trauma around the neck. Examination under general anesthesia and CT scan revealed acquired severe torticollis consistent with Grisel's Syndrome Fielding type 3 accompanied by TB lymphadenitis, and TB myositis of the neck. Manipulation under general anesthesia and immobilization using Minerva cast followed by Lerman Cervicothoracal Osthosis was conducted.

DISCUSSION

This patient was diagnosed with Grisel's syndrome and underwent conservative treatment consisting of reduction under general anesthesia and immobilization using Minerva cast for 6 weeks. The patient was then applied Lherman Cervical Thoracic Orthosis (CTO) halo brace for another 3 months. Anti-tuberculous drug was given to control tuberculous infection. Eight months follow-up showed neither residual deformity, neck pain, nor movement limitation of the neck.

CONCLUSION

Grisel's syndrome has excellent result that is treated with conservative treatment using reduction under general anesthesia and Minerva cast.

摘要

引言

格里塞尔综合征是一种罕见病症,其特征为寰枢关节非创伤性旋转半脱位,由先前头颈部周围炎症引起。它通常见于儿童,表现为斜颈。对于其治疗尚无共识,但早期诊断和治疗至关重要。

病例介绍

一名5岁女孩在结核性淋巴结炎手术切除1天后到门诊就诊,主诉颈部歪斜,且随时间推移病情加重。颈部无创伤史。全身麻醉下检查及CT扫描显示,患有与格里塞尔综合征菲尔丁3型相符的后天性严重斜颈,并伴有结核性淋巴结炎和颈部结核性肌炎。进行了全身麻醉下的手法复位,并使用密涅瓦石膏固定,随后使用勒曼颈胸矫形器。

讨论

该患者被诊断为格里塞尔综合征,并接受了保守治疗,包括全身麻醉下复位及使用密涅瓦石膏固定6周。之后患者又佩戴勒曼颈胸矫形器(CTO)头环支架3个月。给予抗结核药物以控制结核感染。8个月的随访显示,既无残留畸形、颈部疼痛,也无颈部活动受限。

结论

格里塞尔综合征采用全身麻醉下复位及密涅瓦石膏固定的保守治疗效果良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a7/8521141/2310964bd3b5/gr1.jpg

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