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与严重成人发作性哮喘相关的眼周黄色瘤

Periocular xanthogranulomas associated with severe adult-onset asthma.

作者信息

Jakobiec F A, Mills M D, Hidayat A A, Dallow R L, Townsend D J, Brinker E A, Charles N C

机构信息

Massachusetts Eye and Ear Infirmary, Boston.

出版信息

Trans Am Ophthalmol Soc. 1993;91:99-125; discussion 125-9.

Abstract

This article describes six patients who presented, usually bilaterally, with yellow-orange, elevated, indurated, and nonulcerated xanthomatous eyelid lesions, typically extending into the anterior orbital fat, and sometimes involving the extraocular muscles and the lacrimal gland. Because the eyelids remained intact and because the process did not reach the deep orbital and perioptic connective tissues, visual acuity was well preserved. There is cosmetic morbidity and occasionally motility restriction with advancing involvement of the extraocular muscles. All patients had variably severe adult-onset asthma that required treatment with systemic prednisone and inhalants. No evidence of Erdheim-Chester disease was found in any patient, but the appearance in one patient, after 25 years of follow-up, of a separate subcutaneous necrobiotic xanthogranulomatous lesion in the mandibular region with an associated paraproteinemia, suggests that at least some of our cases might be a mild form of necrobiotic xanthogranuloma. For this reason, we would suggest repeated periodic serum protein immunoelectrophoretic studies as well as evaluation for lymphoma. Therapy probably should consist of low doses of periorbital radiotherapy coupled with high doses of corticosteroids. Should this not be successful, then systemic administration of corticosteroids with chemotherapeutic agents might be efficacious, as in necrobiotic xanthogranuloma.

摘要

本文描述了6例患者,其表现通常为双侧黄色橙色、隆起、硬结且无溃疡的睑黄色瘤病变,典型地延伸至眶前脂肪,有时累及眼外肌和泪腺。由于眼睑保持完整,且病变未累及眼眶深部和视神经周围结缔组织,视力得以良好保留。随着眼外肌受累进展,存在美容方面的问题,偶尔还会出现眼球运动受限。所有患者均患有不同程度的成年期起病的严重哮喘,需要全身使用泼尼松和吸入剂治疗。在任何患者中均未发现Erdheim-Chester病的证据,但1例患者在随访25年后,在下颌区域出现了一个单独的皮下坏死性黄色肉芽肿性病变,并伴有副蛋白血症,这表明我们的至少一些病例可能是坏死性黄色肉芽肿的一种轻度形式。因此,我们建议进行反复定期的血清蛋白免疫电泳研究以及淋巴瘤评估。治疗可能应包括低剂量的眶周放疗联合高剂量的皮质类固醇。如果这一方法不成功,那么如同坏死性黄色肉芽肿一样,全身使用皮质类固醇联合化疗药物可能有效。

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