Dasari Suhas P, Jha Pinky
Internal Medicine, Medical College of Wisconsin, Wauwatosa, USA.
Cureus. 2020 Jul 21;12(7):e9326. doi: 10.7759/cureus.9326.
Lemierre's syndrome (LS), once known as "the forgotten disease," is a rare and potentially life-threatening condition that has had a gain in incidence over the last 30 years due to a variety of factors that could include changes in antibody prescription patterns, particularly in regard to the treatment of pharyngitis/tonsillitis. Due to its low incidence and broad spectrum of symptoms, LS does not have an obvious clinical diagnosis and can confuse the clinician managing the patient. Furthermore, it is equally difficult to treat patients suffering from LS as it requires a multidisciplinary approach from multiple subspecialties. Thus, communication between hospitalists, radiologists, otolaryngologists, neurologists, and ophthalmologists is critical towards quickly diagnosing the disease condition so that prompt antibiotics, anticoagulation, and surgical intervention can occur. Atypical presentations can also exist, making the diagnosis and management exponentially more challenging. Ophthalmologic symptoms are a particularly rare and atypical presentation of LS. These rare symptoms in LS can be terrifying for patients and providers alike; yet, there does not seem to be any modern medical literature that summarizes ophthalmologic complications for LS patients. To our knowledge, this is the first systematic review of LS with a focus on ophthalmologic complications that has been done. The main objective of this review paper is to provide an up-to-date literature review of LS epidemiology, pathophysiology, diagnosis, and treatment while also performing a novel systematic review of reported cases of LS with ophthalmological complications. We hope to bring more awareness towards LS and its atypical presentations so that physicians will be better able to rapidly diagnose and treat their patients in order to minimize long-term morbidity and mortality.
勒米尔综合征(LS)曾被称为“被遗忘的疾病”,是一种罕见且可能危及生命的病症。在过去30年里,由于多种因素,包括抗体处方模式的变化,尤其是在咽炎/扁桃体炎治疗方面的变化,其发病率有所上升。由于其发病率低且症状范围广泛,LS没有明显的临床诊断方法,可能会让负责治疗患者的临床医生感到困惑。此外,治疗LS患者同样困难,因为这需要多个亚专业的多学科方法。因此,住院医师、放射科医生、耳鼻喉科医生、神经科医生和眼科医生之间的沟通对于快速诊断病情至关重要,以便能够及时进行抗生素治疗、抗凝治疗和手术干预。非典型表现也可能存在,这使得诊断和管理的难度成倍增加。眼科症状是LS一种特别罕见和非典型的表现。LS中的这些罕见症状对患者和医护人员来说都可能令人恐惧;然而,似乎没有任何现代医学文献总结过LS患者的眼科并发症。据我们所知,这是首次针对LS并聚焦于眼科并发症的系统评价。这篇综述论文的主要目的是提供关于LS流行病学、病理生理学、诊断和治疗的最新文献综述,同时对报告的伴有眼科并发症的LS病例进行新颖的系统评价。我们希望提高对LS及其非典型表现的认识,以便医生能够更好地快速诊断和治疗患者,从而将长期发病率和死亡率降至最低。