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首页> 外文期刊>Pediatric dermatology >Presternal dermoid cyst mimicking lymphatic malformation: a case report and review of the literature.
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Presternal dermoid cyst mimicking lymphatic malformation: a case report and review of the literature.

机译:模仿淋巴畸形的胸骨前皮样囊肿:1例病例报告并文献复习。

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摘要

We describe an 11-month-old boy with an unusually large presternal mass present since birth. The large size, fluctuant properties, transillumination, compressibility, and imaging of this lesion were characteristic of a lymphatic malformation. Although four treatments with sclerotherapy markedly reduced its size, it was not until definitive treatment with surgical excision and the final pathology report that we arrived at the ultimate diagnosis of dermoid cyst. Dermoid cysts, although appearing along embryologic lines of closure, are rarely presternal. They are usually small, thick walled, and filled with sebaceous or keratinous fluid, which typically allows for clinical diagnosis, and show characteristic features on magnetic resonance imaging (MRI) and ultrasound. However, this case illustrates that dermoid cysts can appear in somewhat atypical locations, and imaging is not always diagnostic, so dermoid cyst should remain a part of the differential diagnosis for any lesion presenting midsternally, regardless of the size and imaging characteristics.
机译:我们描述了一个11个月大的男孩,自出生以来就存在异常大的前胸骨肿块。该病变的大尺寸,起伏性,透照性,可压缩性和成像是淋巴畸形的特征。尽管硬化疗法的四种治疗方法可显着缩小其尺寸,但直到通过外科切除术进行明确的治疗以及最终的病理报告才使我们对皮样囊肿进行了最终诊断。皮样囊肿虽然沿闭合的胚胎学系出现,但很少是胸骨前的。它们通常是小而厚的壁,并充满皮脂或角质液,通常可用于临床诊断,并在磁共振成像(MRI)和超声上显示特征。但是,这种情况说明,皮样囊肿可能出现在某些非典型位置,并且影像学并不总是诊断性的,因此对于任何胸骨中部病变,无论大小和影像学特征如何,皮样囊肿均应作为鉴别诊断的一部分。

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