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Erythema Marginatum In A Case Of Post-Streptococcal Arthralgia: A Rash Mimicking Urticaria

机译:链球菌后关节痛一例的红皮:模仿荨麻疹的皮疹

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Erythema marginatum secondary to streptococcal infection is classically associated with acute rheumatic fever and fulfills one of the Jones criteria for this diagnosis. We describe a case of streptococcal associated erythema marginatum without rheumatic heart disease in a 12 year old male with post streptococcal arthralgia and myalgia. The rash was originally suggestive of urticaria. He was initially seen with a five week history of fever. Examination and laboratory evaluation did not yield an acute infectious etiology for his fever. However anti-streptolysin O and anti-deoxyribonuclease B were very elevated. Historically, he had a sore throat 3 weeks prior to his presentation and had been treated by his PCP with amoxicillin; no cultures were done. Based on this history and his elevated anti-streptococcal antibody titers, he was started on cefadroxil and non-steroidal anti-inflammatory drugs. Several days after antibiotics were started and several weeks after his fever and arthralgia symptoms had begun, he developed a trunk and upper arm rash with raised, erythematous borders. Dermatology diagnosed it as urticaria and cetirizine was recommended. The antibiotic was switched to azithromycin but the rash persisted. He was referred to rheumatology who diagnosed a post-streptococcal syndrome. He was started on penicillin under close observation and no changes in the rash were noted. His aches improved in a matter of days. Dermatology biopsied his rash and the histopathology was consistent with both urticaria and published reports of erythema marginatum. Electrocardiogram and serial echocardiographs were normal. His anti-streptococcal titers returned to near normal in 12 months. His elevated inflammatory markers normalized. This case demonstrates a post-streptococcal syndrome with a rash suggestive of urticaria, but was later confirmed to be erythema marginatum in the absence of carditis. Confirming the diagnosis of erythema marginatum was critical, since it enabled a diagnosis of rheumatic fever which had direct implications for prophylactic treatment. Introduction Post-streptococcal syndromes, such as rheumatic fever and post-streptococcal arthritis, have diagnostic criteria. Many post-streptococcal illnesses may not fulfill diagnostic requirements. The breadth of post-streptococcal syndromes is increasingly apparent. Diagnosing a post-streptococcal syndrome is often difficult, not only in meeting criteria but also making a temporal association with streptococcal exposure. The syndromes may overlap in presentation, may be incomplete, or may mimic other systemic disease. We present a case of temporally related post-streptococcal arthralgia and myalgia with erythema marginatium without evidence of carditis. The rash was initially diagnosed as urticaria. Case Presentation A 12 year old male was admitted with no significant past medical history. He first presented to the infectious disease clinic with a five week history of fevers to 103F and a 3 week history of polyarthralgia and myalgia. The joint discomfort was limited to his shoulders, knees, ankles and his mandible area. The discomfort caused him to miss several weeks of school. The pain partially responded to non-steroidal anti-inflammatory drugs (NSAIDs). His review of systems revealed a history of sore throat 3 weeks prior to presentation, which had been treated with amoxicillin. His exam revealed an antalgic gait but no erythema or joint swelling. In addition, no limitation of joint movement was seen. He had no muscle tenderness or weakness on exam. His cardiac, pulmonary, lymphatic and abdominal exams were normal.His workup included an elevated erythrocyte sedimentation rate of 74 mm/hr (0-15 mm/hr), a c-reactive protein of 8.9 mg/dL (<= 0.5 mg/dL), mild anemia with hemoglobin of 11.5 g/dL (12.5-16.1 g/dL), white blood count of 6700 (4000-12,000) and increased platelets at 587,000 (150-400 10-3/mcL). Computed tomography of his mandible, ultrasound of his abdomen, and radiogr
机译:链球菌感染继发的红斑典型地与急性风湿热相关,并且满足该诊断的琼斯标准之一。我们描述了一名12岁男性患有链球菌后关节痛和肌痛而无风湿性心脏病的链球菌相关红斑边缘病例。皮疹最初提示荨麻疹。最初发现他有五个星期的发烧史。体检和实验室评估未发现其发烧的急性感染病因。然而,抗链球菌溶血素O和抗脱氧核糖核酸酶B非常高。从历史上看,他在就诊前三周出现喉咙痛,并接受过阿莫西林治疗。没有文化。基于这一病史和他升高的抗链球菌抗体滴度,他开始使用头孢氨苄和非甾体类抗炎药。在开始使用抗生素几天后,在开始发烧和关节痛症状数周之后,他出现了躯干和上臂皮疹,并出现了红斑的边界。皮肤科诊断为荨麻疹,建议使用西替利嗪。抗生素改用阿奇霉素,但皮疹仍然存在。他被转诊为风湿病科,诊断出链球菌后综合征。在密切观察下,他开始使用青霉素治疗,皮疹未见变化。他的疼痛在几天之内就得到了改善。皮肤科对他的皮疹进行了活检,其组织病理学与荨麻疹和边缘红斑的报道一致。心电图和串行超声心动图检查正常。他的抗链球菌滴度在12个月内恢复到接近正常水平。他的炎症标记升高正常化。该病例显示出链球菌后综合征,并有皮疹提示荨麻疹,但后来在没有心脏病的情况下被证实为边缘性红斑。确认边缘红斑的诊断至关重要,因为它可以诊断风湿热,这直接影响到预防性治疗。简介风湿热和链球菌后关节炎等链球菌后综合征具有诊断标准。许多链球菌后疾病可能无法满足诊断要求。链球菌后综合征的广度越来越明显。诊断链球菌后综合症通常很困难,不仅要满足标准,而且还要与链球菌暴露有暂时的联系。这些综合征可能在表现上重叠,不完整或可能模仿其他全身性疾病。我们提出了一个暂时相关的链球菌性关节痛和肌痛伴红斑边缘性病例,无心脏病的证据。皮疹最初被诊断为荨麻疹。病例介绍一名12岁男性入院,无明显病史。他首先到传染病诊所就诊,发烧至103F已有5周病史,多发痛和肌痛3周病史。关节不适仅限于他的肩膀,膝盖,脚踝和下颌骨区域。不适使他缺课了数周。疼痛对非甾体类抗炎药(NSAIDs)有部分反应。他对系统的检查显示,出现前3周有喉咙痛的病史,已使用阿莫西林治疗。他的检查显示出疼痛的步态,但没有红斑或关节肿胀。另外,没有看到关节运动的限制。他没有肌肉压痛或考试无力。他的心脏,肺,淋巴和腹部检查均正常,他的检查包括红血球沉积速率升高至74 mm / hr(0-15 mm / hr),c反应蛋白为8.9 mg / dL(<= 0.5 mg / dL),轻度贫血,血红蛋白为11.5 g / dL(12.5-16.1 g / dL),白细胞计数为6700(4000-12,000),血小板增加至587,000(150-400 10-3 / mcL)。下颌骨的计算机断层扫描,腹部超声检查和放射线检查

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