CASE REPORT OF UNUSUAL PRESENTATION OF INVASIVE THYMOMA IN A 49 YEARS OLD MALE

D. A. M. Kheiralla
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引用次数: 2

Abstract

Invasive thymomas are rare tumours in the anterior mediastinum, representing 50% of anterior mediastinal masses and about 20-30% of all mediastinal tumours. They are of unknown etiology; about 50% of patients with thymomas are diagnosed incidentally with chest radiography. Thymoma is classified into different stages, which determine the prognosis and type of management, the standard primary treatment for these tumours is Thymectomy. This case study presents a 49 year-old man with unusual presentation of thymoma. On the non-contrast CT images, there was a welldefined heterogeneous anterior mediastinal mass adjacent to the right border of the heart. There was evidence of infiltrations into the anterior mediastinal fat but no mediastinal lymphadenopathy after contrast enhancement, the mass showed heterogeneous enhancement. CT guided trucut tissue biopsy and histological analysis of the mass showed that the tumour consists of neoplastic epithelial cells and non-neoplastic lymphocytes. The findings were consistent with invasive lymphoepithelial thymoma.
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49岁男性罕见侵袭性胸腺瘤病例报告
侵袭性胸腺瘤是发生在前纵隔的罕见肿瘤,约占前纵隔肿块的50%,约占所有纵隔肿瘤的20-30%。病因不明;约50%的胸腺瘤患者是通过胸片偶然诊断出来的。胸腺瘤分为不同的阶段,这决定了预后和治疗类型,这些肿瘤的标准主要治疗是胸腺切除术。这个病例研究报告了一个49岁的男性胸腺瘤的不寻常的表现。在非对比CT图像上,在心脏右侧边界附近有一清晰的不均匀前纵隔肿块。增强后可见前纵隔脂肪浸润,未见纵隔淋巴结病变,肿块呈不均匀强化。CT引导下组织活检及肿块组织学分析显示肿瘤由肿瘤上皮细胞和非肿瘤淋巴细胞组成。结果与浸润性淋巴上皮胸腺瘤一致。
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