首页> 美国卫生研究院文献>International Journal of Environmental Research and Public Health >A Cheek Nodule in a Child: Be Aware of Idiopathic Facial Aseptic Granuloma and Its Differential Diagnosis
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A Cheek Nodule in a Child: Be Aware of Idiopathic Facial Aseptic Granuloma and Its Differential Diagnosis

机译:儿童颊颊结节:注意特发性面部无菌性肉芽肿及其鉴别诊断

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摘要

Background: Idiopathic facial aseptic granuloma (IFAG) is a rare skin disease that typically presents in children with one or more nontender, erythematous to violaceous nodules located on the cheeks or eyelids. Lesions are not accompanied by other skin abnormalities. IFAG remains a diagnostic challenge in pediatric dermatology, because several diseases may present with similar signs. Case presentation: A three-year-old girl with a previous negative clinical history was referred to our hospital for the evaluation of some asymptomatic nodules on the convexity of the left cheek. The nodules had appeared two months before, and had gradually increased in size. Her mother denied any association with trauma or insect bites. The nodules had a hard-elastic consistency, were moderately firm, and were not fluctuant. No associated lymphadenopathy was observed. The girl was afebrile and in good general condition. A histologic evaluation of a biopsy specimen revealed an inflammatory, granulomatous-diffuse infiltrate in the superficial and deep dermis consisting of giant cells, histiocytes, lymphocytes, neutrophils, eosinophils, and plasma cells. The Ziehl–Neelsen stains, Gram-stains, and cultures were negative. Suspecting an IFAG, treatment with topical fusidic acid and oral clarithromycin for 14 days was started. After two months, the lesion resolved and did not recur. Conclusion: This case shows how to differentiate IFAG from other dermatologic diseases associated with a negative evolution. Treatment with oral clarithromycin was effective in our patient. However, more scientific evidence is needed to evaluate the most suitable antibiotic therapy. Further studies are also needed to establish whether antibiotics actually impact IFAG prognosis.
机译:背景:特发性面部无菌性肉芽肿(IFAG)是一种罕见的皮肤病,通常出现在有一个或多个不嫩的儿童中,其红斑性到脸颊或眼睑上的紫红色结节。病变不伴有其他皮肤异常。 IFAG仍然是儿科皮肤病学的诊断挑战,因为几种疾病可能表现出相似的体征。病例介绍:一名三岁以前有阴性临床病史的女孩被转诊到我院,以评估左颊凸面的一些无症状结节。结节在两个月前出现,并逐渐增大。她的母亲否认与创伤或昆虫叮咬有关。结节具有硬弹性的一致性,中等硬度,并且没有波动。没有观察到相关的淋巴结病。这个女孩很发热,身体状况良好。活检标本的组织学评估显示,炎性肉芽肿弥漫性浸润在浅表和深层真皮中,由巨细胞,组织细胞,淋巴细胞,嗜中性粒细胞,嗜酸性粒细胞和浆细胞组成。 Ziehl–Neelsen染色,革兰氏染色和培养物均为阴性。怀疑IFAG,开始用夫西地酸和口服克拉霉素治疗14天。两个月后,病变消退且未复发。结论:本案例说明了如何将IFAG与其他与阴性进化相关的皮肤病相区别。口服克拉霉素治疗对我们的患者有效。但是,需要更多的科学证据来评估最合适的抗生素治疗。还需要进一步研究来确定抗生素是否确实影响IFAG的预后。

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