Acute posterior multifocal placoid pigment epitheliopathy and ulcerative colitis: a possible association.

L. Di Crecchio, M. Parodi, S. Saviano, G. Ravalico
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引用次数: 21

Abstract

PURPOSE To report a case of Acute Posterior Multifocal Placoid Pigment Epitheliopathy (APMPPE) in the course of Ulcerative Colitis (UC). METHODS A complete ophthalmologic evaluation, including fluorescein and indocyanine green angiography, was performed. RESULTS A patient with exacerbation of UC was referred to our department for sudden visual loss in RE. Ophthalmoscopy disclosed multifocal yellow-white placoid lesions typical of APMPPE in RE. There were no lesions in the fellow eye. On fluorescein angiography (FA), the active lesions showed early hypofluorescence, followed by late staining. Indocyanine green angiography (ICGA) revealed early and late hypofluorescence corresponding to the lesions observed clinically, and late anular staining surrounding a hypofluorescent lesion at the posterior pole. On LE ICGA revealed lesions not detected with ophthalmoscopy and FA. After corticosteroid therapy the lesions healed. CONCLUSION Ulcerative Colitis may be responsible for the onset of AMPPPE by an immunological mechanism of delayed type hypersensitivity reaction.
急性后部多灶性placoid色素上皮病与溃疡性结肠炎:可能的关联。
目的报告1例溃疡性结肠炎(UC)病程中出现的急性后部多灶性Placoid Pigment epithelial opathy (APMPPE)。方法采用荧光素和吲哚菁绿血管造影对患者进行全面的眼科检查。结果一名UC加重患者因RE型突发性视力丧失转诊至我科,检出多发黄白色斑块,为典型的RE型APMPPE,伴眼未见病变。在荧光素血管造影(FA)上,活动性病变表现为早期低荧光,随后是晚期染色。吲哚菁绿血管造影(ICGA)显示与临床观察到的病变相对应的早期和晚期低荧光,以及后极低荧光病变周围的晚期环状染色。LE ICGA显示眼底镜和FA未发现的病变。皮质类固醇治疗后病变愈合。结论溃疡性结肠炎可能通过延迟型超敏反应的免疫机制导致AMPPPE的发生。
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