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Ectopic hamartomatous thymoma: report of a case and review of literature

机译:异位错构瘤性胸腺瘤:一例报告并文献复习

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摘要

Ectopic hamartomatous thymoma (EHT) is an exceedingly rare lesion that usually arises in the lower neck and mainly affects adult men. We present the clinicopathological features of a case of EHT in a 28-year-old Chinese male, together with a literature review. Ultrasound imaging and a computed tomography (CT) scan of the neck demonstrated a 3.0-cm well-defined nodule of heterogeneous density located within the left sternocleidomastoid muscle. The patient underwent a gross total resection of the tumor. Grossly, the well-demarcated, encapsulated mass had a predominantly solid and gray-white appearance admixed with microcystic foci filled with serous content and yellowish regions. The lesion consisted of an irregular admixture of spindle cells, epithelium, and mature adipose tissue. Immunohistochemistry showed that both the spindle cell and epithelial components were diffuse and had intense nuclear positivity for p63 and cytoplasmic reactivity for pan-cytokeratin, CK7, and CK19. The patient was followed for 18 months without any evidence of metastasis or recurrence.
机译:异位错构瘤性胸腺瘤(EHT)是一种极为罕见的病变,通常发生在下颈部,主要影响成年男性。我们介绍了一名28岁的中国男性EHT病例的临床病理特征,并进行了文献综述。颈部的超声成像和计算机断层扫描(CT)扫描显示,位于左侧胸锁乳突肌内的3.0厘米界限分明的异质结节。病人接受了肿瘤的大体全切除。总体上,界限分明的,包封的团块主要为实心和灰白色外观,并混有充满浆液含量和淡黄色区域的微囊灶。病变由梭形细胞,上皮和成熟脂肪组织的不规则混合物组成。免疫组织化学显示纺锤体细胞和上皮成分均弥散,对p63具有强烈的核阳性,对泛细胞角蛋白,CK7和CK19具有胞质反应性。对患者进行了18个月的随访,无任何转移或复发的迹象。

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