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一名表现为双侧全葡萄膜炎的儿科患者同时患有强直性脊柱炎和眼弓蛔虫病。

Coexistent Ankylosing Spondylitis and Ocular Toxocariasis in a Pediatric Patient Manifesting As Bilateral Panuveitis.

作者信息

Tanchuling Raymund V, Lopez Juan S, Maliwat Roberto D

机构信息

Ophthalmology, St. Luke's Medical Center, Quezon City, PHL.

Ophthalmology, Nueva Ecija Eye Center, Cabanatuan, PHL.

出版信息

Cureus. 2025 Apr 22;17(4):e82767. doi: 10.7759/cureus.82767. eCollection 2025 Apr.

DOI:10.7759/cureus.82767
PMID:40406765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12096418/
Abstract

The coexistence of ankylosing spondylitis and ocular toxocariasis in the literature is rare and limited to a few case reports. Typically, such cases present as acute nongranulomatous anterior uveitis with  IgG seropositivity. A patient manifesting with findings of both ankylosing spondylitis and toxocariasis bilaterally has not been reported previously in the literature. We present a case of coexistent juvenile spondyloarthritis and ocular toxocariasis in a 16-year-old male presenting with generalized pustules, back pain, peripheral polyarthritis, and bilateral panuveitis. Both eyes displayed abnormalities in the anterior segments, including corectopia, seclusio pupillae, and occlusio pupillae. Posterior segment examination of the right eye showed vitritis, disc edema, and a retinochoroidal granuloma surrounded by infiltrates and perivascular sheathing. A B-scan of the left eye revealed vitritis and the presence of a hyperechoic band from the disc to the retinal periphery. IgG and HLA-B27 were positive, and lumbosacral magnetic resonance imaging confirmed sacroiliitis. Treatment involved subtenon injections of triamcinolone and subcutaneous Etanercept injections, resulting in stabilization of visual acuity. This case highlights the rare co-occurrence of two diseases with overlapping symptoms and uncertain pathogenetic contributions from each to cause the observed manifestations. It supports studies proposing a connection between rheumatic disease and parasitosis.

摘要

文献中强直性脊柱炎与眼弓蛔虫病并存的情况罕见,仅有少数病例报告。通常,此类病例表现为急性非肉芽肿性前葡萄膜炎且IgG血清学呈阳性。此前文献中尚未报道过双侧同时出现强直性脊柱炎和弓蛔虫病表现的患者。我们报告一例16岁男性患者,同时患有幼年型脊柱关节炎和眼弓蛔虫病,表现为全身脓疱、背痛、外周多关节炎和双侧全葡萄膜炎。双眼前段均显示异常,包括瞳孔异位、瞳孔闭锁和瞳孔膜闭。右眼后段检查显示玻璃体炎、视盘水肿以及一个被浸润和血管周围鞘膜包绕的视网膜脉络膜肉芽肿。左眼B超显示玻璃体炎以及从视盘到视网膜周边的高回声带。IgG和HLA - B27呈阳性,并经腰骶部磁共振成像证实存在骶髂关节炎。治疗包括球周注射曲安奈德和皮下注射依那西普,最终视力得以稳定。该病例突出了两种症状重叠疾病罕见的同时发生情况,且每种疾病对所观察到的表现的致病作用尚不明确。它支持了提出风湿性疾病与寄生虫病之间存在关联的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/53f0f9a93617/cureus-0017-00000082767-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/077f2670d8d4/cureus-0017-00000082767-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/0392bf303521/cureus-0017-00000082767-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/497988e54e4f/cureus-0017-00000082767-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/d0537f4da665/cureus-0017-00000082767-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/719a18160fba/cureus-0017-00000082767-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/53f0f9a93617/cureus-0017-00000082767-i06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/077f2670d8d4/cureus-0017-00000082767-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/0392bf303521/cureus-0017-00000082767-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/497988e54e4f/cureus-0017-00000082767-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/d0537f4da665/cureus-0017-00000082767-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/719a18160fba/cureus-0017-00000082767-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a883/12096418/53f0f9a93617/cureus-0017-00000082767-i06.jpg

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本文引用的文献

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