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儿童Grisel综合征:两例病例报告及文献系统综述

Grisel's Syndrome in Children: Two Case Reports and Systematic Review of the Literature.

作者信息

Pini Nicole, Ceccoli Martina, Bergonzini Patrizia, Iughetti Lorenzo

机构信息

Post-Graduated School of Pediatrics, Department of Medical and Surgical Sciences for Mother Children and Adults, University of Modena and Reggio Emilia, Via Del Pozzo 71, Modena 41124, Italy.

Pediatrics Unit, Department of Medical and Surgical Sciences for Mother Children and Adults, University of Modena and Reggio Emilia, Via Del Pozzo 71, Modena 41124, Italy.

出版信息

Case Rep Pediatr. 2020 Nov 12;2020:8819758. doi: 10.1155/2020/8819758. eCollection 2020.

Abstract

. Grisel's syndrome is a rare syndrome characterized by nontraumatic rotatory subluxation of the atlantoaxial joint. It usually affects children and typically presents with torticollis after ear, nose, and throat (ENT) surgery or head and neck infections. In the pediatric literature, there is only a small amount of available data; moreover, no systematic review has been previously done with focus on the pediatric population. We report our experience of two cases, and we provide a systematic review on Grisel's syndrome in children in order to offer a deeper insight about its clinical presentation, its current diagnosis, and principles of treatment. . We describe two boys of 9 and 8 years old, who developed atlantoaxial subluxation after adenoidectomy. Considering the early diagnosis, a conservative treatment was chosen, with no recurrence and no sequelae at follow-up. We identified 114 case reports, of which 90 describe children, for a total of 171 pediatric patients. Of the 154 cases in which cause was reported, 59.7% presented a head and neck infection and 35.7% had previous head and neck surgery. There is no sex prevalence (49.7% males versus 50.2% females). Mean delay in diagnosis is 33 days. Eight % of the patients had neurological impairment of the 165 cases which mentioned treatment, 96% underwent a conservative treatment, of whom the 8.8% recurred with the need of surgery. As a whole, 12% underwent surgery as a first- or second-line treatment. 3 6% of the patients whose follow-up was reported developed a sequela, minor limitation of neck movement being the most frequent. . Grisel's syndrome should be suspected in children with painful unresponsive torticollis following ENT procedures or head and neck inflammation. CT scan with 3D reconstruction is the gold standard for diagnosis, allowing the identification of the subluxation and the classification according to the Fielding-Hawkins grading system. Surgical treatment is indicated in case of high-grade instability or failure of conservative treatment. Review of the literature shows how early diagnosis based on clinical and radiological evaluation is crucial in order to avoid surgical treatment and neurologic sequelae.

摘要

格里斯尔综合征是一种罕见的综合征,其特征为寰枢关节非创伤性旋转半脱位。它通常影响儿童,典型表现为在耳鼻喉(ENT)手术后或头颈部感染后出现斜颈。在儿科文献中,仅有少量可用数据;此外,之前尚未针对儿科人群进行过系统综述。我们报告两例病例的经验,并对儿童格里斯尔综合征进行系统综述,以便更深入地了解其临床表现、当前诊断及治疗原则。我们描述了两名分别为9岁和8岁的男孩,他们在腺样体切除术后发生了寰枢椎半脱位。考虑到早期诊断,选择了保守治疗,随访时无复发且无后遗症。我们识别出114例病例报告,其中90例描述的是儿童,共计171例儿科患者。在报告病因的154例病例中,59.7%有头颈部感染,35.7%曾接受过头颈部手术。无性别差异(男性占49.7%,女性占50.2%)。诊断的平均延迟时间为33天。在提及治疗的165例病例中,8%的患者有神经功能损害,96%接受了保守治疗,其中8.8%复发且需要手术治疗。总体而言,12%的患者接受了手术作为一线或二线治疗。报告了随访情况的患者中,36%出现了后遗症,颈部活动轻度受限最为常见。对于耳鼻喉手术后或头颈部炎症后出现疼痛性、无反应性斜颈的儿童,应怀疑格里斯尔综合征。三维重建CT扫描是诊断的金标准,可识别半脱位并根据菲尔丁 - 霍金斯分级系统进行分类。对于高级别不稳定或保守治疗失败的情况,需进行手术治疗。文献综述表明,基于临床和影像学评估的早期诊断对于避免手术治疗和神经后遗症至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f076/7676959/134efb9cc142/CRIPE2020-8819758.001.jpg

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