Micronodular Thymoma with Lymphoid Stroma: A Case Report

H. Song, Joungho Han, Taesung Kim
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引用次数: 4

Abstract

Micronodular thymoma with lymphoid stroma (MNT) is an extremely rare tumor and has not been reported in Korea. Herein, we report a case of MNT diagnosed in a 75 year-old male. The mass was incidentally identified on thoracic computer tomography (CT) during work-up for a cardiac mass. The resected thymic mass was ovoid and solid measuring 3.5×3 cm in size and showed homogenously white tan, solid and firm cut surface. Microscopically, the tumor had a thin fibrous capsule except small foci of invasion to thymic adipose tissue, and consisted of characteristic multiple discrete epithelial nodules in abundant lymphoid stroma. The epithelial nests anastomosed each other, forming a vague cord-like structure. The cells in the epithelial nests were bland, spindle to oval shape with relatively abundant cytoplasm, slightly vesicular chromatin and one definite nucleolus. The lymphoid stroma contained prominent germinal centers. No evidence of recurrence or metastasis has been found within 4 years of surgery.
小结节性胸腺瘤伴淋巴间质1例
小结节性胸腺瘤伴淋巴样基质瘤(MNT)是一种极为罕见的肿瘤,在韩国尚未见报道。在此,我们报告一个病例MNT诊断在一个75岁的男性。肿块是在检查心脏肿块时偶然在胸部计算机断层扫描(CT)上发现的。切除的胸腺肿块卵圆形,实性,大小3.5×3 cm,呈均匀的白褐色,切面结实。显微镜下,肿瘤除浸润胸腺脂肪组织的小灶外,呈薄纤维包膜,在丰富的淋巴样基质中由特征性的多个离散上皮结节组成。上皮巢相互吻合,形成模糊的绳状结构。上皮巢内细胞色淡,梭形至卵圆形,细胞质较丰富,染色质微泡状,核仁明确。淋巴样基质含有突出的生发中心。手术后4年内未发现复发或转移的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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