Thymic carcinoma - a rare case report.

Clujul medical (1957) Pub Date : 2018-01-01 Epub Date: 2018-04-25 DOI:10.15386/cjmed-887
Nidhi Bansal, Arnav Kr Roychoudhury, Harshi Dhingra
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引用次数: 3

Abstract

Introduction: Thymic carcinoma is a rare, invasive mediastinal neoplasm with a tendency to metastasize. They constitute a heterogeneous group of tumors that present differently in terms of both behavior and prognosis.

Case report: We present a case of thymic carcinoma in a 55-year-old male patient known to suffer from Myasthenia gravis, whose chief complaints were fatigability, ptosis and coughing. All electromyography studies were done along with excision biopsy to reach the definitive diagnosis.

Results and conclusion: The histopathological diagnosis of Thymic carcinoma-Lymphoepithelial variant was established. Though no definite staging system exists for the thymic carcinoma, prognosis of the patient was ascertained by using Weissferdt-Moran system, Masaoka and Tsuchiya TNM staging systems. Involvement of the pleural and the pericardial structures leads to poor prognosis, though no distant metastases or lymph nodal metastasis were evident.

Abstract Image

Abstract Image

胸腺癌1例报告。
胸腺癌是一种罕见的纵隔浸润性肿瘤,有转移倾向。它们构成了一组异质性的肿瘤,在行为和预后方面表现不同。病例报告:我们报告一例胸腺癌在一个55岁的男性患者已知遭受重症肌无力,其主诉是疲劳,上睑下垂和咳嗽。所有肌电图研究与切除活检一起进行,以达到明确的诊断。结果与结论:建立了胸腺癌淋巴上皮变异的组织病理学诊断。虽然胸腺癌没有明确的分期系统,但采用Weissferdt-Moran分期系统、Masaoka分期系统和Tsuchiya分期系统来确定患者的预后。虽然没有明显的远处转移或淋巴结转移,但累及胸膜和心包结构导致预后不良。
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