Pradeep Thanuja Gopal, Shetti Samyakta A
Department of Ophthalmology Ramaiah Medical College Hospital, Bengaluru, Karnataka, India.
Taiwan J Ophthalmol. 2021 Jun 26;12(2):184-190. doi: 10.4103/tjo.tjo_13_21. eCollection 2022 Apr-Jun.
To describe the ocular manifestations in the acute stage of Stevens-Johnson syndrome/ toxic epidermal necrolysis.
We reviewed all the medical records of patients diagnosed with Stevens-Johnson syndrome/ toxic epidermal necrolysis and erythema multiforme between 2012 and 2019. Demographics, ophthalmic manifestations, and the treatment given systemically and locally were reviewed and analyzed.
We had forty-five patients admitted to our hospital between Jan 2012 to Dec 2019 with SJS/TEN as a diagnosis.Twenty-six (57.5%) of them were females, and 19(42.2%) were males. The mean age was 27.5 years.Forty (88.9%) of our cases were diagnosed as Stevens-Johnson syndrome, and five (11.9%) as toxic epidermal necrolysis. We found antiepileptics as a triggering agent in thirteen cases (28.8%). Fever (84.4%) and mucosal lesions (86.7%) were the most common presenting symptom. We found ocular symptoms in only 22 (48.9%) patients. The treating physicians referred only thirty-one cases to the ophthalmologist, out of which 22 cases were referred within three days of admission. The most common ocular involvement was conjunctival congestion (69%). Ocular grading showed that mild grade included 42.9%, moderate grade 28.6%, and severe grade 28.6% of the cases. The ocular treatment involved medical management with lubricating drops (100%), topical steroids (58.6%), and topical antibiotics (68.9%). Five individuals with a severe grade of ocular involvement underwent amniotic membrane transplantation.
Ocular examination and grading are essential in the acute stage of SJS/TEN. It helps the ophthalmologist recognize the sentinel findings and institute appropriate treatment in the acute stage as early as possible.
描述史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症急性期的眼部表现。
我们回顾了2012年至2019年间诊断为史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症和多形红斑患者的所有病历。对人口统计学、眼部表现以及全身和局部治疗情况进行了回顾和分析。
2012年1月至2019年12月期间,我院收治了45例诊断为史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症的患者。其中26例(57.5%)为女性,19例(42.2%)为男性。平均年龄为27.5岁。我们的病例中有40例(88.9%)被诊断为史蒂文斯-约翰逊综合征,5例(11.9%)为中毒性表皮坏死松解症。我们发现13例(28.8%)病例的诱发因素为抗癫痫药。发热(84.4%)和黏膜病变(86.7%)是最常见的首发症状。我们仅在22例(48.9%)患者中发现了眼部症状。治疗医生仅将31例患者转诊至眼科医生处,其中22例在入院后三天内转诊。最常见的眼部受累表现为结膜充血(69%)。眼部分级显示,轻度病例占42.9%,中度病例占28.6%,重度病例占28.6%。眼部治疗包括使用润滑滴眼液(100%)、局部类固醇(58.6%)和局部抗生素(68.9%)进行药物治疗。5例重度眼部受累患者接受了羊膜移植。
在史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症急性期,眼部检查和分级至关重要。这有助于眼科医生识别哨兵发现,并尽早在急性期进行适当治疗。