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泪腺炎作为疑似CREST综合征患者罕见的首发表现。

Dacryoadenitis as a Rare Initial Presentation in a Patient with Suspected Crest Syndrome.

作者信息

Singh Arkaja, Rao Sameer, Shah Riya, Maheshwari Mashal, Dhillon Aarish, Gupta Silka

机构信息

Department of Medicine, Mahatma Gandhi Medical College, Jaipur, India.

Department of Medicine, Rutgers New Jersey Medical School, Newark, USA.

出版信息

Eur J Case Rep Intern Med. 2024 Sep 19;11(10):004801. doi: 10.12890/2024_004801. eCollection 2024.

Abstract

UNLABELLED

Systemic sclerosis (SSc) is a rare, chronic disease with diverse clinical presentations, and only a few cases with ocular manifestations have been reported in the literature. In this case report, we describe the case of a 51-year-old South Asian woman who initially complained of painless swelling in her left upper eyelid. An ultrasound examination of the left eye revealed an enlarged lacrimal gland with increased vascularity. The presence of dacryoadenitis, which was unresponsive to initial conservative management with oral antibiotics and warm compresses, along with positive antinuclear antibodies, prompted further investigation. Dacryoadenitis or orbital inflammation is a common presentation in systemic conditions such as Sjogren's syndrome, systemic lupus erythematosus, sarcoidosis, or granulomatosis with polyangiitis. However, it can also be a rare initial symptom in a patient with CREST syndrome. To our knowledge, this is only the second case in the literature of dacryoadenitis in the context of calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome. This case highlights the significance of serological markers and peripheral clinical presentations in individuals with chronic orbital inflammation, emphasizing the importance of considering further systemic associations.

LEARNING POINTS

Recognize that although CREST syndrome is primarily characterized by its hallmark features - calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia - it can also present with additional clinical features that may indicate the onset or presence of the syndrome. Bilateral dacryoadenitis can be challenging to diagnose due to its overlapping symptoms with other orbital or systemic conditions. The case report may highlight the importance of differentiating it from conditions like orbital cellulitis, sarcoidosis, or lymphoproliferative disorders. Advanced imaging techniques (like magnetic resonance imaging or computed tomography scans) and careful assessment of clinical history (including systemic symptoms like fever or autoimmune conditions) are crucial for accurate diagnosis. The case report underscores the need for tailored management strategies for bilateral dacryoadenitis, from conservative treatments in mild cases to more aggressive therapies in severe ones, while also highlighting the importance of monitoring for complications and being vigilant about atypical presentations, such as those seen in patients with CREST syndrome.

摘要

未标注

系统性硬化症(SSc)是一种罕见的慢性疾病,临床表现多样,文献中仅报道了少数有眼部表现的病例。在本病例报告中,我们描述了一名51岁南亚女性的病例,她最初主诉左上眼睑无痛性肿胀。左眼超声检查显示泪腺肿大且血管增多。泪腺炎的存在,对最初口服抗生素和热敷的保守治疗无反应,同时抗核抗体呈阳性,促使进一步检查。泪腺炎或眼眶炎症是干燥综合征、系统性红斑狼疮、结节病或显微镜下多血管炎等全身性疾病的常见表现。然而,它也可能是CREST综合征患者罕见的初始症状。据我们所知,这是文献中第二例在钙质沉着、雷诺现象、食管动力障碍、指(趾)硬皮病和毛细血管扩张(CREST)综合征背景下出现泪腺炎的病例。该病例强调了血清学标志物和外周临床表现对于慢性眼眶炎症患者的重要性,强调了考虑进一步全身性关联的重要性。

学习要点

认识到尽管CREST综合征主要以其标志性特征——钙质沉着、雷诺现象、食管动力障碍、指(趾)硬皮病和毛细血管扩张——为特征,但它也可能出现其他临床特征,这些特征可能表明该综合征的发作或存在。双侧泪腺炎由于其与其他眼眶或全身性疾病症状重叠,诊断可能具有挑战性。该病例报告可能强调了将其与眼眶蜂窝织炎、结节病或淋巴增殖性疾病等疾病区分开来的重要性。先进的成像技术(如磁共振成像或计算机断层扫描)以及对临床病史的仔细评估(包括发热或自身免疫性疾病等全身性症状)对于准确诊断至关重要。该病例报告强调了针对双侧泪腺炎需要制定个性化的管理策略,从轻度病例的保守治疗到重度病例的更积极治疗,同时也强调了监测并发症以及警惕非典型表现(如CREST综合征患者所见)的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c377/11451854/bef45d17e4e7/4801_Fig1.jpg

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