Coviltir Valeria, Burcel Miruna Gabriela, Marinescu Maria Cristina, Urse Bianca Maria, Danielescu Ciprian
Ophthalmology Discipline, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
Clinical Hospital for Ophthalmological Emergencies, 010464 Bucharest, Romania.
Diagnostics (Basel). 2024 Oct 16;14(20):2303. doi: 10.3390/diagnostics14202303.
We report a case of a 16-year-old girl presenting to our clinic with decreased visual acuity and increased intraocular pressure in both eyes. The ophthalmological examination revealed best-corrected visual acuity (BCVA) of 0.3 in the right eye (R.E.) and 0.4 in the left eye (L.E.) and intraocular pressure (IOP) of 46 mmHg in the R.E. and 42 mmHg in the L.E., with a 360° closed angle on gonioscopy, pupillary block due to bulging, a hyper-spherical lens and high corneal thickness, without ectopia lentis or cataract. The eyes responded poorly to pharmacological mydriasis; therefore, the lens equator could not be visualised. The patient had a history of pulmonary stenosis, short stature and no significant cognitive deficits. These elements point to the diagnosis of Weill-Marchesani syndrome, and the ophthalmological management was surgical, including lens extraction and the installation of a capsular tension ring, an intraocular lens and a Shunt ExPress implantation. Evolution was favourable, with improved BCVA of 0.7 in the R.E. and 0.63 in the L.E. and IOP of 14 mmHg in the R.E. and 13 mmHg in the L.E., without topical or systemic treatment at the 6-month follow-up. Weill-Marchesani syndrome has a complex presentation, with ophthalmological, musculoskeletal, cardiac and psychiatric manifestations. Usually, this leads to a need for a multidisciplinary approach. The ophthalmologic symptoms are often the cause of presentation to a specialist, and glaucoma is the most threatening of the ocular pathologies, with possible evolution into irreversible blindness; therefore, prompt surgery and careful follow-up become key components of the treatment plan. As a take-home message, we encourage a high degree of suspicion of Weill-Marchesani syndrome in such cases.
我们报告了一例16岁女孩,因双眼视力下降和眼压升高前来我院就诊。眼科检查显示,右眼最佳矫正视力(BCVA)为0.3,左眼为0.4,右眼眼压(IOP)为46 mmHg,左眼为42 mmHg,前房角镜检查显示360°闭角,因晶状体膨隆导致瞳孔阻滞,晶状体呈高度球形且角膜厚度增加,无晶状体异位或白内障。双眼对药物散瞳反应不佳,因此无法观察到晶状体赤道部。患者有肺动脉狭窄和身材矮小病史,无明显认知缺陷。这些表现提示诊断为Weill-Marchesani综合征,眼科治疗采取手术方式,包括晶状体摘除、植入囊袋张力环、人工晶状体和ExPress分流器。病情进展良好,随访6个月时,右眼BCVA提高到0.7,左眼提高到0.63,右眼眼压为14 mmHg,左眼眼压为13 mmHg,无需局部或全身治疗。Weill-Marchesani综合征临床表现复杂,有眼科、肌肉骨骼、心脏和精神方面的表现。通常,这需要多学科方法进行治疗。眼科症状往往是患者就诊于专科医生的原因,青光眼是最具威胁性的眼部疾病,可能发展为不可逆性失明;因此,及时手术和仔细随访成为治疗方案的关键组成部分。作为重要提示,我们鼓励在此类病例中高度怀疑Weill-Marchesani综合征。