Khan Alishba Ashraf, Mumtaz Shamaila, Malik Javeria, Manzoor Muhammad Shahzad, Maqbool Faran, Shafique Mudassir, Nazir Maheen, Ibn-E-Shad Zohad, Kandel Kamal
Rawalpindi Medical University Rawalpindi Pakistan.
NESCOM Hospital Islamabad Pakistan.
Clin Case Rep. 2024 Feb 23;12(2):e8554. doi: 10.1002/ccr3.8554. eCollection 2024 Feb.
This unique case report of primary Sjogren's syndrome (pSS) shows bilateral ptosis and significant periorbital edema, compromising vision. To avoid misleading diagnosis, antibody tests must be evaluated and interpreted in the context of clinical findings.
Primary Sjögren's syndrome is an idiopathic, autoimmune disorder involving the lacrimal and salivary glands characterized by both localized and systemic manifestations including xerostomia and keratoconjunctivitis sicca. Myasthenia Gravis (MG) is also an autoimmune disorder characterized by the development of auto-antibodies against nicotinic acetylcholine receptors that causes decreased muscle response to stimulation. It usually presents with ptosis and generalized body weakness. Ophthalmological involvement is common in both disorders but ptosis is very rarely seen in pSS. We report the case of a 27-year-old woman presenting to our clinic with the complaint of ptosis and eyelid swelling. She also had a positive anti-acetylcholine receptor antibody test and her initial presentation mimicked Myasthenia Gravis. Her autoimmune workup revealed a positive titer of Anti Ro SSA antibodies. Myasthenia Gravis was ruled out on electrodiagnostic studies which showed no decremental response, and pSS was confirmed on lip biopsy. Our case highlights that it is important to interpret the antibody test results in the context of clinical findings as we can have spurious results in autoimmune diseases. Autoimmune conditions can have varying presenting complaints hence, clinical judgment should always overrule diagnostic investigations and should thus guide patient management.
这例原发性干燥综合征(pSS)的独特病例报告显示双侧上睑下垂和明显的眶周水肿,影响视力。为避免误诊,必须结合临床发现对抗体检测结果进行评估和解读。
原发性干燥综合征是一种特发性自身免疫性疾病,累及泪腺和唾液腺,其特征为包括口干和干眼症在内的局部及全身表现。重症肌无力(MG)也是一种自身免疫性疾病,其特征是产生针对烟碱型乙酰胆碱受体的自身抗体,导致肌肉对刺激的反应降低。它通常表现为上睑下垂和全身无力。眼科受累在这两种疾病中都很常见,但上睑下垂在原发性干燥综合征中非常罕见。我们报告了一例27岁女性患者,因上睑下垂和眼睑肿胀前来我院就诊。她的抗乙酰胆碱受体抗体检测也呈阳性,其初始表现类似重症肌无力。她的自身免疫检查显示抗Ro SSA抗体滴度呈阳性。电诊断研究排除了重症肌无力,因为未显示递减反应,唇活检确诊为原发性干燥综合征。我们的病例强调,在临床发现的背景下解读抗体检测结果很重要,因为在自身免疫性疾病中我们可能会得到假阳性结果。自身免疫性疾病可能有不同的临床表现,因此,临床判断应始终优先于诊断检查,并应指导患者的治疗管理。