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眼眶木村病:使用霉酚酸酯的维持治疗

Orbital Kimura disease: maintenance therapy using mycophenolate mofetil.

作者信息

Fenech Matthew, Ajanaku Ayodeji, McCormick Austin, Coupland Sarah E, Krishna Yamini, Sultan Ziyaad, Ghadiri Nima

机构信息

Department of Ophthalmology, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Department of Histopathology, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

出版信息

Orbit. 2025 Apr;44(2):215-222. doi: 10.1080/01676830.2024.2358061. Epub 2024 May 30.

Abstract

Kimura disease (KD) is a rare, chronic, inflammatory condition, predominantly found in male patients of Asian ethnicity. It typically presents between 50-60 years of age and usually with bilateral disease. Angiolymphoid hyperplasia with eosinophilia (ALHE) remains the main differential diagnosis, although histological analysis is essential in differentiating from other similarly presenting pathologies. In this case, we present an atypical case of unilateral orbital KD in a middle-aged, Caucasian, male gentleman and no evidence of regional lymphadenopathy along with a literature review of orbital KD and the differential diagnoses, histological features and management modalities available, adding to the sparse literature on the topic. At present, no recognised diagnostic criteria for KD are available, with histopathological analysis through incisional or excisional biopsy being the primary diagnostic method. Complete surgical excision with or without corticosteroid management remains the most common treatment modality although management is shifting to steroid-sparing immunomodulatory therapy. To the best of our knowledge, this is the first case to describe maintenance therapy of KD using mycophenolate mofetil.

摘要

木村病(KD)是一种罕见的慢性炎症性疾病,主要见于亚洲种族的男性患者。它通常在50至60岁之间出现,且通常为双侧病变。伴有嗜酸性粒细胞增多的血管淋巴样增生(ALHE)仍然是主要的鉴别诊断疾病,尽管组织学分析对于与其他表现相似的病理情况进行鉴别至关重要。在此病例中,我们报告了一名中年白人男性单侧眼眶KD的非典型病例,且无区域淋巴结病证据,并对眼眶KD及鉴别诊断、组织学特征和可用的治疗方式进行了文献综述,这为该主题的稀少文献增添了内容。目前,尚无公认的KD诊断标准,通过切开活检或切除活检进行组织病理学分析是主要的诊断方法。无论是否联合使用皮质类固醇治疗,完整的手术切除仍然是最常见的治疗方式,尽管治疗方式正转向保留类固醇的免疫调节疗法。据我们所知,这是第一例描述使用霉酚酸酯进行KD维持治疗的病例。

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