Isolated clival Langerhans cell histiocytosis in a pediatric patient: systematic review and illustrative case report.

IF 1.2
Adam M Abdallah, Atef F Hulliel, Tala Y Dabash, Dana Saleh, Sarah Al Sharie, Maysa Al-Hussaini, Mouness Obeidat
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引用次数: 0

Abstract

Background: Langerhans cell histiocytosis is a rare clonal myeloid disorder with heterogeneous clinical manifestations, predominantly affecting children. Osseous involvement is common; however, isolated localization to the clivus is exceptionally rare and poses significant diagnostic and therapeutic challenges due to its proximity to critical neurovascular structures. We present an illustrative pediatric case alongside a systematic review of the literature to better characterize this uncommon entity.

Method: This study presents a rare case of a 3.5-year-old boy diagnosed with isolated clival Langerhans cell histiocytosis confirmed by histopathological and immunohistochemical evaluation. In addition, we systematically reviewed 11 published studies encompassing 11 patients with histologically confirmed isolated clival LCH. The systematic review adhered to PRISMA guidelines, with a comprehensive literature search conducted in PubMed and Scopus using predefined keywords related to Langerhans cell histiocytosis and clival involvement.

Results: Eleven published cases met inclusion criteria. Most patients were pediatric, with a slight female predominance. Abducens nerve palsy and diplopia were the most frequent presenting symptoms. Imaging typically demonstrated osteolytic clival lesions that mimicked chordoma and other skull base tumors. Histopathology consistently showed characteristic LCH morphology with CD1a and S100 positivity. Management strategies varied and included biopsy, surgical resection, chemotherapy, and radiotherapy. Outcomes were favorable in most cases, with significant neurological improvement and no reported recurrences during follow-up.

Conclusion: Isolated clival LCH is an exceptionally rare presentation that can radiologically mimic aggressive skull base neoplasms. Histopathological confirmation is essential. Early recognition and appropriate multidisciplinary management are associated with favorable outcomes.

一例小儿患者孤立的斜坡朗格汉斯细胞组织细胞增多症:系统回顾和说明性病例报告。
背景:朗格汉斯细胞组织细胞增多症是一种罕见的克隆性骨髓疾病,临床表现不均匀,主要影响儿童。骨性受累是常见的;然而,孤立定位于斜坡是非常罕见的,并提出了重大的诊断和治疗挑战,由于其接近关键的神经血管结构。我们提出了一个说明性的儿科病例,并对文献进行了系统的回顾,以更好地表征这种不常见的实体。方法:本研究报告一例罕见的3.5岁男孩,经组织病理学和免疫组织化学评估证实为孤立性斜坡朗格汉斯细胞组织细胞增多症。此外,我们系统地回顾了11项已发表的研究,其中包括11例组织学证实的孤立性斜坡LCH患者。系统评价遵循PRISMA指南,在PubMed和Scopus中进行了全面的文献检索,使用与朗格汉斯细胞组织细胞增生症和clival累及相关的预定义关键词。结果:11例已发表病例符合纳入标准。大多数患者为儿科,女性略占优势。外展神经麻痹和复视是最常见的症状。影像学典型表现为骨溶解性斜坡病变,类似脊索瘤和其他颅底肿瘤。组织病理学一致显示CD1a和S100阳性的特征性LCH形态。治疗策略多种多样,包括活检、手术切除、化疗和放疗。大多数病例的预后良好,随访期间神经系统有显著改善,无复发报告。结论:孤立的斜坡LCH是一种非常罕见的表现,放射学上可以模拟侵袭性颅底肿瘤。组织病理学证实是必要的。早期识别和适当的多学科管理与良好的结果相关。
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