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伴有嗜酸性粒细胞增多的眼眶血管淋巴样增生症。表现为睑板腺囊肿。

Orbital angiolymphoid hyperplasia with eosinophilia. Presentation as chalazion.

作者信息

Archer K F, Hurwitz J J, Heathcote G

机构信息

Department of Ophthalmology, University of Texas Health Science Center, San Antonio.

出版信息

Ophthalmic Plast Reconstr Surg. 1991;7(3):208-21. doi: 10.1097/00002341-199109000-00010.

DOI:10.1097/00002341-199109000-00010
PMID:1911528
Abstract

Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon, benign slow-growing lesion primarily found in the head and neck region, with onset between the third and fourth decades, and a female predominance in the nonOriental population. Kimura's disease, occurring primarily in young Oriental males, is a similar lesion with peripheral blood eosinophilia, regional lymphadenopathy, and occasional nephrotic syndrome. Orbital ALHE is rare, previously reported in only nine patients. Orbital ALHE is a solitary lesion, with an older age of onset, between the fourth and eighth decades, than ALHE elsewhere. There is a male predominance, in contradistinction to ALHE elsewhere in nonOrientals. Orbital ALHE demonstrates the same histology as other locations, with exuberant capillary proliferation and an inflammatory infiltrate of eosinophils, lymphocytes, plasma cells, and mast cells. The maturity of the lesion, not necessarily the duration, determines the presence of lymphoid follicles and germinal centers. A distinctive endothelial cell lines and even extends into the vascular lumens. Peripheral blood eosinophilia occasionally occurs, and a few cases have been reported in conjunction with asthma. Therapeutic regimens for ALHE include excision, carbon dioxide and argon laser, irradiation, steroids, electrodesiccation, and cytotoxic agents. Orbital lesions have been treated successfully with excision, or biopsy with debulking, or steroids.

摘要

嗜酸性粒细胞增多性血管淋巴样增生(ALHE)是一种罕见的、生长缓慢的良性病变,主要见于头颈部,发病年龄在第三和第四个十年之间,在非东方人群中女性占主导。木村病主要发生在年轻的东方男性中,是一种类似的病变,伴有外周血嗜酸性粒细胞增多、局部淋巴结病,偶尔伴有肾病综合征。眼眶ALHE很罕见,此前仅报道过9例。眼眶ALHE是一种孤立性病变,发病年龄比其他部位的ALHE大,在第四和第八个十年之间。与非东方人其他部位的ALHE不同,眼眶ALHE以男性为主。眼眶ALHE的组织学表现与其他部位相同,有丰富的毛细血管增生以及嗜酸性粒细胞、淋巴细胞、浆细胞和肥大细胞的炎性浸润。病变的成熟度而非持续时间决定了淋巴滤泡和生发中心的存在。有一种独特的内皮细胞系,甚至延伸到血管腔。外周血偶尔会出现嗜酸性粒细胞增多,有少数病例报告与哮喘有关。ALHE的治疗方案包括切除、二氧化碳和氩激光治疗、放疗、类固醇、电干燥和细胞毒性药物。眼眶病变已通过切除、或减瘤活检、或类固醇治疗成功治愈。

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Ophthalmic Plast Reconstr Surg. 1991;7(3):208-21. doi: 10.1097/00002341-199109000-00010.
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引用本文的文献

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Angiolymphoid Hyperplasia of the Orbit: A Rare Case Report and Review of the Literature.眼眶血管淋巴样增生症:1例罕见病例报告及文献复习
Indian J Otolaryngol Head Neck Surg. 2023 Jun;75(2):967-970. doi: 10.1007/s12070-022-03171-5. Epub 2022 Nov 5.
2
Angiolymphoid hyperplasia with eosinophilia: a case series and literature review.血管淋巴样增生伴嗜酸性粒细胞增多症:病例系列及文献复习。
Int Ophthalmol. 2023 Jul;43(7):2457-2467. doi: 10.1007/s10792-023-02644-y. Epub 2023 Mar 4.
3
Angiolymphoid hyperplasia with eosinophilia of the eyelid and orbit: the Western cousin of Kimura's disease?
眼睑及眼眶嗜酸性粒细胞增多性血管淋巴样增生:木村病的西方同类疾病?
Int Ophthalmol. 2014 Feb;34(1):107-10. doi: 10.1007/s10792-013-9741-7. Epub 2013 Mar 5.