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双侧成人眼球表面黄色肉芽肿,怀疑为厄德里希-切斯特病。

Bilateral adult epibulbar xanthogranulomas suspicious for Erdheim-Chester disease.

作者信息

Aggarwal Shruti, Jakobiec Frederick A, Hamrah Pedram

机构信息

*Ocular Surface Imaging Center; †Cornea & Refractive Surgery Service, Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, MA; ‡Department of Ophthalmology, Harvard Medical School, Boston, MA; and §Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, MA.

出版信息

Cornea. 2014 Oct;33(10):1113-7. doi: 10.1097/ICO.0000000000000191.

Abstract

PURPOSE

The aim of this study was to report the clinical, imaging, and histopathological findings of bilateral, conjunctival adult-onset xanthogranulomas that raised the prospect of a mild form of Erdheim-Chester disease.

METHODS

This is a case report.

RESULTS

A 35-year-old white male complaining of ocular irritation, presented with bilateral, nasal and temporal, yellow, elevated conjunctival lumps first noticed 1.5 years back, which were not associated with other ocular findings. The lesions were firm, attached to the underlying episclera, and measured 1.1 × 0.9, 1.1 × 0.8, 1.2 × 0.5, and 0.5 × 0.5 cm in the temporal and nasal right and left eyes, respectively. Each mass was fleshy with vascularity at the peripheral margin. Histopathologic evaluation after excisional biopsy revealed lipidized xanthoma cells, multiple Touton giant cells, and lymphocytes. Immunohistochemical staining was positive for adipophilin (lipid), CD68, CD163 histiocytes, CD3 T cells (with CD8 cytotoxic T cells > CD4 T-helper cells), and virtually no CD20 B cells or IgG4 plasma cells. The patient later acquired similar xanthogranulomatous subcutaneous lesions on the extremities. Positron emission tomography scans showed sclerosis in the medullary cavities of the tibia and the radius of both legs and arms, and an absence of retroperitoneal lesions. A normal serum immunoelectrophoresis and the absence of a BRAF gene mutation were demonstrated.

CONCLUSIONS

Adult-onset xanthogranuloma can present as a solitary conjunctival mass without periocular or orbital involvement. The clinical, histopathologic, and radiologic findings in this case are suggestive of Erdheim-Chester disease without displaying any life-threatening lesions to date. Histopathologic and imaging studies can help in obtaining a diagnosis. Ophthalmologists should be aware that xanthogranulomatous conditions may have potential systemic implications, and a thorough systemic evaluation is recommended for lesions that initially seemed to be isolated in nature.

摘要

目的

本研究旨在报告双侧结膜成人起病的黄色瘤的临床、影像学和组织病理学表现,这些表现提示了一种轻度形式的厄尔德海姆-切斯特病。

方法

这是一篇病例报告。

结果

一名35岁的白人男性,主诉眼部刺激症状,双侧鼻侧和颞侧出现黄色、隆起的结膜肿物,于1.5年前首次发现,未伴有其他眼部表现。病变质地坚硬,附着于下方的巩膜,右眼颞侧、鼻侧肿物大小分别为1.1×0.9 cm、1.1×0.8 cm,左眼颞侧、鼻侧肿物大小分别为1.2×0.5 cm、0.5×0.5 cm。每个肿物质地似肉,周边有血管。切除活检后的组织病理学评估显示有脂质化的黄色瘤细胞、多个图顿巨细胞和淋巴细胞。免疫组化染色显示亲脂素(脂质)、CD68、CD163组织细胞、CD3 T细胞(CD8细胞毒性T细胞>CD4辅助性T细胞)呈阳性,几乎没有CD20 B细胞或IgG4浆细胞。该患者后来在四肢出现了类似的黄色瘤性皮下病变。正电子发射断层扫描显示双侧腿部胫骨和手臂桡骨髓腔内有硬化,且无腹膜后病变。血清免疫电泳正常,未检测到BRAF基因突变。

结论

成人起病的黄色瘤可表现为孤立的结膜肿物,不累及眼周或眼眶。该病例的临床、组织病理学和影像学表现提示为厄尔德海姆-切斯特病,迄今为止未显示任何危及生命的病变。组织病理学和影像学研究有助于做出诊断。眼科医生应意识到黄色瘤性疾病可能有潜在的全身影响,对于最初看似孤立的病变,建议进行全面的全身评估。

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