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双侧成人起病性眼眶黄色瘤:一例报告

Bilateral Adult-Onset Orbital Xanthogranuloma: A Case Report.

作者信息

Chen Yue, Gao Aili, Tian Xin

机构信息

Department of Dermatology, Guangzhou Institute of Dermatology, Guangzhou, People's Republic of China.

出版信息

Clin Cosmet Investig Dermatol. 2023 Dec 13;16:3575-3580. doi: 10.2147/CCID.S437616. eCollection 2023.

Abstract

Adult-onset xanthogranuloma (AOX) is one of the four rare syndromes collectively referred to as adult xanthogranulomatous disease (AXD). It primarily occurs in the orbit and ocular adnexa and displays distinctive histopathological features, characterized by the infiltration of non-Langerhans-derived foam-like histiocytes and Touton giant cells. The presence of diffuse yellow plaques on the eyelids serves as a highly indicative feature. In this report, we present a compelling case of bilateral periorbital AOX. Initially, the patient received a diagnosis of necrotizing xanthogranuloma (NBX) and underwent treatment with dapsone, which yielded a poor response. Subsequently, through repeated biopsy, immunoprotein electrophoresis, and high-throughput sequencing, the diagnosis was revised to AOX. Subsequently, the patient's treatment was modified to include oral hormone therapy, and no further progression of the periorbital plaque was observed. Notably, the patient's sister was diagnosed with xanthelasma palpebrarum (XP), suggesting a potential genetic association between AOX and XP. Unfortunately, the sister declined further histologic examination and genetic sequencing of her skin lesions, impeding the acquisition of additional evidence regarding the genetic link between these two disorders. Despite the divergent pathological features, pathogenesis, and clinical presentation of AOX and xanthelasma palbrarum, clinicians should remain cognizant of the plausible genetic correlation between these two conditions and pursue further investigations when feasible.

摘要

成人起病性黄色瘤病(AOX)是统称为成人黄色瘤病(AXD)的四种罕见综合征之一。它主要发生于眼眶及眼附属器,具有独特的组织病理学特征,表现为非朗格汉斯来源的泡沫样组织细胞和杜顿巨细胞浸润。眼睑上出现弥漫性黄色斑块是一个极具指示性的特征。在本报告中,我们展示了一例双侧眶周AOX的典型病例。最初,患者被诊断为坏死性黄色瘤病(NBX)并接受了氨苯砜治疗,但效果不佳。随后,通过反复活检、免疫蛋白电泳和高通量测序,诊断被修正为AOX。随后,患者的治疗方案改为口服激素治疗,眶周斑块未再进一步进展。值得注意的是,患者的姐姐被诊断为睑黄瘤(XP),提示AOX与XP之间可能存在遗传关联。不幸的是,姐姐拒绝了对其皮肤病变进行进一步的组织学检查和基因测序,这阻碍了获取这两种疾病之间遗传联系的更多证据。尽管AOX和睑黄瘤在病理特征、发病机制和临床表现上存在差异,但临床医生应认识到这两种疾病之间可能存在的遗传相关性,并在可行时进行进一步调查。

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