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小儿霍纳综合征:是否总是需要进行潜在恶性肿瘤的检查?

Paediatric Horner's syndrome: is investigation for underlying malignancy always required?

机构信息

Department of Pediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK.

Department of Paediatric Surgery, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.

出版信息

Arch Dis Child. 2019 Oct;104(10):984-987. doi: 10.1136/archdischild-2019-317007. Epub 2019 Jun 11.

DOI:10.1136/archdischild-2019-317007
PMID:31186293
Abstract

OBJECTIVE

Horner's syndrome (HS) is characterised by a triad of ocular miosis, ptosis and anhidrosis. HS may be a subtle sign of occult pathology in otherwise asymptomatic children, neuroblastoma (NBL) being the the most common associated malignant tumour. Despite such knowledge, the incidence of underlying malignancy in children with HS remains unclear and robust evidence to guide best clinical practice is sparse. We performed a systematic review of the literature with the aim of identifying the incidence of NBL in children with HS of unknown aetiology, and establishing if screening for NBL should be routinely performed in this patient population.

METHODS

Systematic review of the literature (PubMed and Ovid/Medline database, 1961-2018).

RESULTS

The initial search identified 334 manuscripts, of which 8 studies were included in the final analysis. All reports were single-centre retrospective studies without control groups and included a total of 152 patients (age range 0-20 years). All studies investigated patients with HS but without previously established diagnosis. In the studies included, 17 out of a total of 152 patients were diagnosed with a space-occupying lesion. 12 out of the 152 patients were subsequently detected with NBL.

CONCLUSION

HS in children may be the first sign of occult malignancy. We report the first systematic review that comprehensively investigates the incidence of malignancy in this unique patient cohort. We show that HS of unknown aetiology in children warrants further investigation(s) to exclude an underlying space-occupying lesion. This should include cross-sectional imaging of the brain, neck and thorax, plus urinary catecholamines for prompt diagnosis and treatment.

摘要

目的

霍纳氏综合征(HS)的特征是眼裂缩小、上睑下垂和无汗三联征。HS 可能是其他无症状儿童隐匿性病理的一个微妙迹象,神经母细胞瘤(NBL)是最常见的相关恶性肿瘤。尽管有这样的认识,但 HS 儿童中潜在恶性肿瘤的发病率仍不清楚,缺乏指导最佳临床实践的有力证据。我们对文献进行了系统回顾,旨在确定病因不明的 HS 儿童中 NBL 的发病率,并确定是否应常规对该患者人群进行 NBL 筛查。

方法

文献系统回顾(PubMed 和 Ovid/Medline 数据库,1961-2018 年)。

结果

最初的搜索确定了 334 篇手稿,其中 8 项研究纳入最终分析。所有报告均为无对照组的单中心回顾性研究,共纳入 152 例患者(年龄 0-20 岁)。所有研究均调查了 HS 患者,但无先前确定的诊断。在所纳入的研究中,152 例患者中有 17 例被诊断为占位性病变。152 例患者中有 12 例随后被诊断为 NBL。

结论

儿童中的 HS 可能是隐匿性恶性肿瘤的首发症状。我们报告了第一项全面调查这一独特患者群体中恶性肿瘤发病率的系统评价。我们表明,病因不明的儿童 HS 需要进一步检查以排除潜在的占位性病变。这应包括脑、颈部和胸部的横断面成像,以及尿儿茶酚胺以进行快速诊断和治疗。

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Paediatric Horner's syndrome: is investigation for underlying malignancy always required?小儿霍纳综合征:是否总是需要进行潜在恶性肿瘤的检查?
Arch Dis Child. 2019 Oct;104(10):984-987. doi: 10.1136/archdischild-2019-317007. Epub 2019 Jun 11.
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