Horner's syndrome after an ultrasound-guided fine-needle aspiration puncture of a thyroid nodule.

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM
Alexandra Abegão Matias, Teresa Sabino, José Silva-Nunes
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引用次数: 0

Abstract

Summary: Horner's syndrome is a rare condition that results from damage to the oculosympathetic chain. The classical presentation consists of miosis, unilateral ptosis and hemifacial anhidrosis due to a deficiency of sympathetic activity. Although it has been described as a result of different types of trauma, we present the first clinical report of Horner's syndrome that was developed after a fine-needle aspiration puncture of a thyroid nodule. A 48-year-old woman with a non-toxic multinodular goiter underwent an ultrasound-guided fine-needle aspiration for the second time for a nodule located at the right thyroid lobe. Four hours after the procedure, she developed homolateral eyelid ptosis, miosis and enophthalmos and went to the emergency department for observation. Structural causes potentially related to the manifestations were excluded. Horner's syndrome was diagnosed and the patient was discharged with symptomatic measures. Three months after the event, the patient reported partial improvement. We discuss the pathophysiology associated with Horner's syndrome, the association with thyroid diagnostic and therapeutic procedures, clinical presentation, patient management and prognosis. Although fine-needle aspiration of a thyroid nodule has few associated complications, Horner's syndrome should be considered when the patient develops ophthalmologic symptoms. Preventive measures should be observed to minimize its occurrence.

Learning points: Horner's syndrome is a potential complication of diagnostic and therapeutic procedures directed at the thyroid gland, including ultrasound-guided fine-needle aspiration. It is characterized by eyelid ptosis, miosis, enophthalmos and anhidrosis homolateral to the lesion. The diagnosis of Horner's syndrome is clinical after excluding structural causes and establishing the temporal relationship between the procedure and the manifestations. There is no targeted treatment for Horner's syndrome, but it can be prevented.

超声引导下细针穿刺甲状腺结节后出现霍纳综合征。
摘要:霍纳氏综合征是一种罕见的由眼交感神经链损伤引起的疾病。典型的表现包括瞳孔缩小、单侧上睑下垂和由于交感神经活动不足而引起的面肌无汗。虽然它被描述为不同类型的创伤的结果,我们提出的第一个临床报告的霍纳综合征,是在细针穿刺甲状腺结节后发展起来的。一位48岁的女性,患有无毒多结节性甲状腺肿,在超声引导下第二次行细针穿刺治疗位于右侧甲状腺叶的结节。术后4小时,患者出现同侧眼睑下垂、瞳孔缩小、眼球内陷,到急诊科观察。排除了可能与表现相关的结构性原因。经诊断为霍纳综合征,患者经对症治疗出院。事件发生三个月后,患者报告部分改善。我们讨论与霍纳综合征相关的病理生理学,与甲状腺诊断和治疗方法的关系,临床表现,患者管理和预后。虽然细针穿刺甲状腺结节很少有相关并发症,但当患者出现眼科症状时应考虑霍纳综合征。应采取预防措施,尽量减少其发生。学习要点:霍纳综合征是针对甲状腺的诊断和治疗程序的潜在并发症,包括超声引导的细针穿刺。它的特点是眼睑下垂,缩小,眼球内陷和无汗同侧病变。霍纳综合征的诊断是在排除结构性原因并建立手术与表现之间的时间关系后的临床诊断。目前还没有针对霍纳氏综合症的治疗方法,但它是可以预防的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
142
审稿时长
9 weeks
期刊介绍: Endocrinology, Diabetes & Metabolism Case Reports publishes case reports on common and rare conditions in all areas of clinical endocrinology, diabetes and metabolism. Articles should include clear learning points which readers can use to inform medical education or clinical practice. The types of cases of interest to Endocrinology, Diabetes & Metabolism Case Reports include: -Insight into disease pathogenesis or mechanism of therapy - Novel diagnostic procedure - Novel treatment - Unique/unexpected symptoms or presentations of a disease - New disease or syndrome: presentations/diagnosis/management - Unusual effects of medical treatment - Error in diagnosis/pitfalls and caveats
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