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以持续性耳漏伴外耳道肉芽样组织为表现的颅底朗格汉斯细胞组织细胞增多症。

Skull base Langerhans cell histiocytosis presenting as persistent ear discharge with granulation-like tissue in the external ear canal.

作者信息

Saad Marwa Mohammed Elrashreed, Thompson Christopher S G, Alsalem Mohammad

机构信息

Alder Hey Children's Hospital, Liverpool, Merseyside, UK.

Alder Hey Children's Hospital, Liverpool, Merseyside, UK

出版信息

BMJ Case Rep. 2025 Jun 22;18(6):e263728. doi: 10.1136/bcr-2024-263728.

Abstract

Langerhans cell histiocytosis (LCH) is a neoplastic disease characterised by the deposition of granulomatous lesions in various tissues in the body. LCH of the lateral skull base commonly presents with scalp lesions, post-auricular lesions, otalgia and persistent ear infections. A toddler was brought to the ENT clinic with persistent left ear canal granulation tissue and bloody and malodorous discharge. After failed medical treatment with antibiotic and steroid topical drops. The ear was examined under general anaesthesia. Large friable granulation tissue was seen obstructing the external auditory canal extending to the tympanic membrane. Histological examination of the surgical specimen revealed CDa-1-positive cells, diagnostic of LCH. There were widespread enhancing tissues throughout the skull base bilaterally on CT. She was diagnosed with multiple bone LCH, enrolled in the LCH-IV trial and started on chemotherapy. This case highlights the importance of histological and radiological diagnosis of granulation tissue after failed medical treatment.

摘要

朗格汉斯细胞组织细胞增多症(LCH)是一种肿瘤性疾病,其特征是肉芽肿性病变沉积于身体的各种组织中。侧颅底LCH通常表现为头皮病变、耳后病变、耳痛和持续性耳部感染。一名幼儿因左耳耳道持续存在肉芽组织以及血性、恶臭分泌物被带到耳鼻喉科诊所。在使用抗生素和类固醇外用滴剂进行药物治疗失败后,在全身麻醉下对耳朵进行了检查。可见大量易碎的肉芽组织阻塞外耳道并延伸至鼓膜。手术标本的组织学检查显示CDa-1阳性细胞,确诊为LCH。CT显示双侧颅底有广泛的强化组织。她被诊断为多骨LCH,参加了LCH-IV试验并开始化疗。该病例突出了在药物治疗失败后对肉芽组织进行组织学和放射学诊断的重要性。

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本文引用的文献

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