Isolated Abducens Nerve Palsy in an Adolescent With Confounding Multisystem Serology: A Case Report and Diagnostic Review.

IF 0.5 Q4 PEDIATRICS
Case Reports in Pediatrics Pub Date : 2025-09-24 eCollection Date: 2025-01-01 DOI:10.1155/crpe/2146062
Roberto Paparella, Irene Bernabei, Fabiola Panvino, Camilla Ajassa, Lorenzo Benedetti, Lucia Leonardi, Alberto Spalice, Luigi Tarani
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Abstract

Cranial nerve palsies in pediatric patients are rare and can be challenging to diagnose due to the broad spectrum of potential causes, including infections, inflammation, neoplasms, and idiopathic conditions. Abducens nerve palsy (ANP), though uncommon, is of particular interest due to its association with both intracranial and systemic pathologies. We present the case of a 16-year-old male who developed isolated left ANP of presumed infectious-inflammatory origin. Initial neurological and ophthalmological assessments revealed esotropia and marked abduction deficit without other cranial nerve involvement. Brain magnetic resonance imaging showed enhancement of the left abducens nerve consistent with neuritis, while cerebrospinal fluid analysis and initial laboratory investigations were unremarkable. Serological testing revealed low-positive IgM for Mycoplasma pneumoniae, Chlamydia pneumoniae, Herpes simplex virus (HSV)-1/2, and Borrelia burgdorferi, while polymerase chain reaction for HSV and Borrelia were negative. The patient was treated with corticosteroids, antibiotics, and antivirals, showing mild improvement in eye mobility, and follow-up imaging revealed resolution of the inflammatory changes. Despite persistent low IgM positivity in subsequent tests, the patient fully recovered within 6 months. Although the exact etiology remains unclear, the combination of clinical response and serological findings suggests a possible infectious or immune-mediated process. This case underscores the diagnostic complexity of pediatric ANP and highlights the importance of considering a broad differential diagnosis and using a multidisciplinary approach in management. Further research is needed to better understand the role of mild serological findings and improve diagnostic strategies for such conditions.

青少年孤立性外展神经麻痹伴混淆多系统血清学:1例报告及诊断回顾。
脑神经麻痹在儿科患者中是罕见的,并且由于潜在原因广泛,包括感染、炎症、肿瘤和特发性疾病,诊断可能具有挑战性。外展神经麻痹(ANP)虽然不常见,但由于其与颅内和全身病理相关,因此引起了特别的关注。我们提出的情况下,一个16岁的男性谁发展孤立的左ANP推定感染性炎症的起源。最初的神经学和眼科评估显示内斜视和明显的外展缺陷,没有其他脑神经受累。脑磁共振成像显示左外展神经增强与神经炎一致,而脑脊液分析和初步实验室检查无明显差异。血清学检测肺炎支原体、肺炎衣原体、单纯疱疹病毒(HSV)-1/2和伯氏疏螺旋体IgM低阳性,HSV和伯氏疏螺旋体聚合酶链反应阴性。患者接受皮质类固醇、抗生素和抗病毒药物治疗,眼活动能力轻度改善,随访影像学显示炎症改变消退。尽管在随后的测试中IgM持续呈低阳性,但患者在6个月内完全康复。虽然确切的病因尚不清楚,但临床反应和血清学结果表明可能是感染或免疫介导的过程。该病例强调了儿科ANP诊断的复杂性,并强调了考虑广泛的鉴别诊断和使用多学科方法进行管理的重要性。需要进一步的研究来更好地了解轻度血清学结果的作用,并改进对此类疾病的诊断策略。
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
自引率
11.10%
发文量
48
审稿时长
13 weeks
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