Orbital Cellulitis Secondary to Dacryocystitis: A Case Series and Literature Review.

IF 1.2 4区 医学 Q3 OPHTHALMOLOGY
Michéal O'Rourke, Yi Fan Tang, Zelda Pick, Jennifer S Tan, Priscilla E Z Tan, Dnyaneshwar D Athavale, Brett O'Donnell, Dinesh Selva, Adam Gajdatsy, Thomas G Hardy, Alan McNab, Jwu Jin Khong
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Abstract

Purpose: This study aimed to determine risk factors, and describe management and outcomes in patients who developed orbital cellulitis secondary to dacryocystitis.

Methods: Multicenter retrospective case series with 18 patients and review of published cases.

Results: The mean age was 62 years, 56% were female and 50% had recurrent dacryocystitis. Visual acuity was reduced in the affected eye with a mean of 0.27 logMAR (Snellen 20/40) which improved to 0.15 logMAR (Snellen 20/30) at final follow up. Two cases (12%) had dacryoliths and 1 patient had sarcoidosis within the lacrimal sac. Gram-positive bacteria were identified in 73% (11/15), gram-negative bacteria in 13% (2/15), and mixed infection in 13% (2/15), respectively. Cases who had dacryocystorhinostomy as definitive treatment, either acutely (n = 3) or electively (n = 10) had full resolution. Transcutaneous drainage of the medial wall abscess in 10 patients helped resolve acute cellulitis. Four patients declined dacryocystorhinostomy after transcutaneous drainage; 2 had repeated dacryocystitis and orbital cellulitis, while 2 had no further infective episodes. One immunosuppressed patient had rapid progression to non-perception-of-light vision due to fungal invasion. Forty-six published cases reported up to 28% permanent loss of vision (perception-of-light and non-perception-of-light). Dacryoliths were discovered in 17% of published cases.

Conclusions: Orbital cellulitis complicating dacryocystitis appears to be related to recurrent dacryocystitis and possibly the presence of dacryoliths. Immunosuppression is identified as a poor prognostic factor in this series. While transcutaneous drainage works well as a temporizing measure, dacryocystorhinostomy either done acutely or deferred until resolution of orbital cellulitis is required for definitive cure.

眼眶蜂窝织炎继发于泪囊炎:病例系列及文献回顾。
目的:本研究旨在确定泪囊炎继发眼眶蜂窝织炎患者的危险因素,并描述治疗和预后。方法:18例患者的多中心回顾性病例系列,并复习已发表的病例。结果:平均年龄62岁,女性占56%,复发性泪囊炎占50%。患眼视力下降,平均0.27 logMAR (Snellen 20/40),最终随访时改善至0.15 logMAR (Snellen 20/30)。2例(12%)有泪石,1例泪囊内有结节病。革兰氏阳性菌占73%(11/15),革兰氏阴性菌占13%(2/15),混合感染占13%(2/15)。将泪囊鼻腔造口术作为最终治疗的病例,无论是急性治疗(n = 3)还是选择性治疗(n = 10),均有完全缓解。经皮内侧壁脓肿引流术治疗急性蜂窝织炎10例。经皮引流泪囊鼻腔造口术4例;2例反复发生泪囊炎和眶蜂窝织炎,2例无进一步感染发作。一名免疫抑制患者因真菌侵袭而迅速发展为无光视觉。46例已发表的病例报告高达28%的永久性视力丧失(光感和无光感)。已发表的病例中有17%发现泪石。结论:眼眶蜂窝织炎合并泪囊炎可能与泪囊炎复发有关,也可能与泪石的存在有关。免疫抑制被认为是一个预后不良的因素。虽然经皮引流作为一种临时措施效果很好,但泪囊鼻腔造口术可以急性进行,也可以推迟到眼眶蜂窝织炎消退后才能最终治愈。
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来源期刊
CiteScore
2.50
自引率
10.00%
发文量
322
审稿时长
3-8 weeks
期刊介绍: Ophthalmic Plastic and Reconstructive Surgery features original articles and reviews on topics such as ptosis, eyelid reconstruction, orbital diagnosis and surgery, lacrimal problems, and eyelid malposition. Update reports on diagnostic techniques, surgical equipment and instrumentation, and medical therapies are included, as well as detailed analyses of recent research findings and their clinical applications.
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