Purtscher-like Retinopathy in a Patient with Acute Alcoholic Pancreatitis and a Literature Review.

IF 3.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Vesela Todorova Mitkova-Hristova, Marin Anguelov Atanassov, Yumyut Remzi Idriz, Steffanie Hristova Hristova
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引用次数: 0

Abstract

Background and Clinical Significance: Purtscher-like retinopathy is a rare occlusive microangiopathy that causes sudden vision loss of varying severity. It presents with diverse retinal findings, such as cotton-wool spots, haemorrhages, and optic disc and macular edema, among others. A key characteristic is the absence of trauma. This condition has been observed in patients with acute pancreatitis, renal failure, preeclampsia, HELLP syndrome, childbirth, and other systemic disorders. Case Presentation: A 35-year-old male presented with complaints of seeing spots in front of both eyes, with a duration of ten days following the initiation of treatment for acute alcoholic pancreatitis. On examination, best-corrected visual acuity (BCVA) in both eyes was 5/6. Fundus examination revealed multiple cotton-wool spots and haemorrhages located in the posterior pole and around the optic disc, more pronounced in the left eye, where the optic disc had blurred margins and the macular reflex was absent. Perimetry showed paracentral scotomas, and optical coherence tomography (OCT) revealed thickening and disruption of the inner retinal layers in the papillomacular region of both eyes. Fundus fluorescein angiography demonstrated adequate perfusion of the vascular network, with hypofluorescent areas in the arteriovenous phase, peripapillary and in the papillomacular zone, due to masking by cotton-wool spots and haemorrhages. Treatment included systemic antiplatelet agents, anticoagulants, and vitamins, along with topical non-steroidal anti-inflammatory drugs. Two months after the initial presentation visual acuity improved to 6/6 in both eyes. Follow-up OCT scans showed atrophy of the inner retinal layers corresponding to the previous cotton-wool spot and the areas of reduced light sensitivity on perimetry had decreased in size. Conclusions: Acute pancreatitis is the most common systemic condition associated with the development of Purtscher-like retinopathy. Timely diagnosis and management of the underlying systemic disease are essential for preventing ocular complications. Ophthalmological evaluation is necessary in patients with acute pancreatitis who present with visual symptoms in order to detect this often-overlooked rare condition.

急性酒精性胰腺炎患者的purtscher样视网膜病变及文献综述
背景和临床意义:purtscher样视网膜病变是一种罕见的闭塞性微血管病变,可导致不同程度的突然视力丧失。它表现为多种视网膜表现,如棉絮斑、出血、视盘和黄斑水肿等。一个关键特征是没有创伤。这种情况在急性胰腺炎、肾衰竭、子痫前期、HELLP综合征、分娩和其他全身性疾病患者中都有观察到。病例介绍:一名35岁男性,在开始治疗急性酒精性胰腺炎后持续10天,主诉双眼前可见斑点。经检查,双眼最佳矫正视力(BCVA)为5/6。眼底检查发现眼底后极及视盘周围有多处棉絮斑及出血,左眼更为明显,视盘边缘模糊,黄斑反射消失。眼部检查显示中心旁暗瘤,光学相干断层扫描(OCT)显示双眼乳头状斑区视网膜内层增厚和破裂。眼底荧光素血管造影显示血管网络灌注充足,在动静脉期、乳头周围和乳头状带,由于被棉线斑点和出血掩盖,荧光较低。治疗包括全身抗血小板药物,抗凝血剂,维生素,以及局部非甾体抗炎药。初次出现后两个月,双眼视力改善至6/6。后续的OCT扫描显示视网膜内层萎缩,对应于先前的棉絮斑,眼部检查光敏性降低的区域大小减小。结论:急性胰腺炎是与purtscher样视网膜病变发展相关的最常见的全身性疾病。及时诊断和治疗潜在的全身性疾病对于预防眼部并发症至关重要。眼科评估是必要的急性胰腺炎患者谁目前的视觉症状,以发现这种经常被忽视的罕见情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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