一个病例报告:一名鼻窦水肿诊断较晚的儿童出现间歇性内斜视和共济失调

A. Omari, P. B. Toft, C. von Buchwald
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摘要

背景:急性细菌性鼻窦炎是一种常见病,患儿常伴有一个或多个鼻窦粘膜炎症。在出现潜在的严重化脓性并发症之前,孤立的蝶窦感染可能会表现出不典型或无症状。意识到并发症的早期征兆对于避免延误转诊、诊断和治疗至关重要。我们首次详细报道了一名患有蝶窦水肿的儿童,其症状为间歇性单侧内斜视、肢体和步态共济失调。本病例强调了识别非典型表现的必要性,有助于早期诊断和治疗,防止出现严重的、可能危及生命的并发症。病例介绍:一名 7 岁女孩以前身体健康,但几个月来身体状况每况愈下,表现为全身不适、体重明显下降和反复上呼吸道感染。尽管曾多次到基层医疗机构就诊,但由于感染指标正常,医生没有开抗生素。随后,患者出现间歇性复视,遂转至儿科急诊。检查发现他步态宽大,指鼻指和膝跟测试共济失调,左眼间歇性内斜。其他神经系统检查均无异常。因怀疑颅内病变而进行了脑部造影检查,发现左侧蝶窦内有孤立性水肿。经过内窥镜鼻窦手术和抗生素治疗,患者在一个月内完全康复。经检查发现,该患者可能因感染引发了适应性内斜,并成功地使用眼镜进行了治疗。结论本病例表明,蝶窦孤立性水肿是导致间歇性内斜、肢体和步态共济失调的潜在原因。该病例提醒临床医生警惕化脓性并发症的早期征兆,及时进行诊断和治疗,以防延误诊断和出现严重并发症。该报告提倡在对大脑进行常规扫描的同时,也对蝶窦进行成像,因为患者有可能因神经症状而怀疑颅内病变而被转诊。
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Intermittent esotropia and ataxia in a child with late diagnosis of empyema in the sphenoid sinus - a case report
Background: Acute bacterial rhinosinusitis is a common condition often affecting children with inflammation of the mucous membrane in one or more nasal sinuses. Isolated sphenoid sinus infections can exhibit atypical or no symptoms before potentially severe suppurative complications develop. Awareness of early signs of complications is crucial to avoid delays in referral, diagnosis, and treatment. We present the first detailed report of a child with sphenoid sinus empyema with the symptoms intermittent unilateral esotropia and limb and gait ataxia. This case emphasizes the need to recognise atypical presentations, aiding early diagnosis and treatment to prevent severe, possibly life-threatening complications. Case presentation: A 7-year-old girl, previously healthy, presented with a months-long decline in health marked by general malaise, significant weight loss, and recurrent upper respiratory infections. Despite multiple primary care visits no antibiotics were prescribed because infection parameters were found to be normal. Subsequently, the emergence of intermittent double vision prompted referral to the pediatric emergency department. Examination revealed a wide-based gait, ataxic finger-nose-finger and knee-heel tests, and intermittent esotropia of the left eye. Neurological examination was otherwise unremarkable. Imaging of the cerebrum was performed on the suspicion of intracranial pathology and found isolated empyema within the left sphenoid sinus. Endoscopic sinus surgery and antibiotic treatment led to a full recovery within a month. The accommodative esotropia, likely triggered by the infection, was identified, and successfully treated with spectacles. Conclusion: This case recognises isolated empyema in the sphenoid sinus as a potential cause of intermittent esotropia and limb and gait ataxia. It serves as a reminder for clinicians to be vigilant for early signs of suppurative complications to commence prompt diagnosis and treatment to prevent delayed recognition and severe complications. It advocates the inclusion of images of the sphenoid sinus to accompany the conventional scans of the cerebrum, as patients risk referral on the suspicion of intracranial pathology on the basis of neurological symptoms.
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