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首页> 外文期刊>BMC Ophthalmology >Old-age-onset subconjunctival juvenile xanthogranuloma without limbal involvement
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Old-age-onset subconjunctival juvenile xanthogranuloma without limbal involvement

机译:没有角膜缘累及的老年性结膜下少年黄肉芽肿

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Background Juvenile xanthogranuloma (JXG) is a benign idiopathic cutaneous granulomatous tumor occurring primarily in infants less than 1 year old, and less commonly found in older children and adults. To date, however, there have been no reports of patients aged >50?years with cornealscleral JXG without limbal involvement. We describe here a 58-year-old woman with subconjunctival JXG without limbal involvement. Case presentation A 58-year-old female was referred for evaluation of a subconjunctival mass in her left eye, found incidentally 2?weeks earlier. Examination revealed a protruding yellow-orange subconjunctival mass just below the 6-o’clock limbus of her left eye, measuring 6.0?×?4.5?mm, but not extending into the cornea. The overlying conjunctival epithelium was intact, and a feeding vessel was observed between the mass and the episclera. The subconjunctival lesion was excised under local anesthesia, by dissecting the mass from the overlying conjunctiva and underlying sclera. The conjunctiva was reattached to the sclera without creating a bare area. Hematoxylin and eosin-stained sections showed that the mass was a mixed inflammatory lesion containing dense infiltrations of epithelioid histiocytes with foamy cytoplasm, lymphocytes, and plasma cells, as well as multinucleated Touton giant cells with the characteristic circumferential ring of nuclei. Immunohistochemical staining showed that the lesion was positive for the macrophage marker CD68 and negative for the Langerhans cell markers S-100 protein and CD1a, indicating that the lesion was a xanthogranuloma. The patient has been followed up for 12-months without recurrence. Conclusions JXG can occur as a solitary subconjunctival mass even in older adults, and immunohistochemistry is useful in differential diagnosis. Simple excision with careful dissection may be effective for subconjunctival JXG.
机译:背景技术少年黄肉芽肿(JXG)是一种良性特发性皮肤肉芽肿性肿瘤,主要发生在1岁以下的婴儿中,在大龄儿童和成人中较少见。然而,迄今为止,尚无年龄大于50岁的角膜巩膜JXG患者没有角膜缘受累的报道。我们在这里描述了一名58岁的结膜下JXG患者,没有角膜缘受累。病例介绍一名58岁的女性被转诊评估其左眼结膜下肿块,偶然发现是在2周前。检查发现在左眼角膜缘6点正下方有一个突出的橙橙色结膜下肿块,大小为6.0?×?4.5?mm,但未延伸到角膜。上面的结膜上皮完好无损,并且在肿块和巩膜之间观察到了食管。结膜下病变在局部麻醉下切除,方法是将肿块从上方的结膜和下方的巩膜中解剖出来。结膜重新附着在巩膜上,而没有形成裸露区域。苏木精和曙红染色切片显示,肿块是混合的炎性病变,其中含有上皮样组织细胞的浓密浸润,带有泡沫细胞质,淋巴细胞和浆细胞,以及具有核周环特征的多核Touton巨细胞。免疫组织化学染色显示,该病变的巨噬细胞标记CD68为阳性,而朗格汉斯细胞标记的S-100蛋白和CD1a为阴性,表明该病变为黄原肉芽肿。对该患者进行了12个月的随访,无复发。结论JXG甚至可以在老年人中以结膜下结节的形式出现,免疫组化在鉴别诊断中很有用。简单切除并仔细解剖可能对结膜下JXG有效。

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