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原发性胸腺腺癌:16 例临床病理和免疫组化研究,重点关注分化的形态谱。

Primary thymic adenocarcinomas: a clinicopathological and immunohistochemical study of 16 cases with emphasis on the morphological spectrum of differentiation.

机构信息

Department of Pathology, The University of Texas, MD Anderson Cancer Center.

Department of Pathology, The University of Texas, MD Anderson Cancer Center.

出版信息

Hum Pathol. 2018 Apr;74:73-82. doi: 10.1016/j.humpath.2018.01.011. Epub 2018 Jan 12.

DOI:10.1016/j.humpath.2018.01.011
PMID:29339175
Abstract

Sixteen cases of primary thymic adenocarcinoma are presented. The patients are 9 men and 7 women between the ages of 22 and 68 years (average, 45 years) who presented with non-specific symptoms including cough, chest pain, and dyspnea. Diagnostic imaging revealed the presence of an anterior mediastinal mass, which was surgically removed in all of the patients. Histologically, none of the tumors was encapsulated and showed different growth patterns including mucinous, non-mucinous, and papillary features. The majority of cases showed mixed growth pattern, and the tumor was limited to the mediastinum with only a few cases extending to lymph nodes or pericardium. In two cases, the adenocarcinoma was associated with a thymoma. Immunohistochemical stains were performed, and their positive staining varied depending on the histology of the tumors, showing positive staining in some cases for keratin 7, keratin 20, CEA, CD5, CD117, and CDX-2. PAX8 and TTF-1 were negative in all the tumors. Follow-up information was obtained in 10 patients over a period of 1 to 12 years, indicating that three patients had died within a period of 14 months, one with brain metastasis, while seven patients have remained alive without recurrence. The cases herein described span the spectrum of thymic epithelial tumors and highlight the importance of recognizing this particular type of carcinoma, as it may follow a different outcome and require different treatment options.

摘要

本文报道了 16 例原发性胸腺腺癌。患者为 9 名男性和 7 名女性,年龄 22 岁至 68 岁(平均 45 岁),表现为咳嗽、胸痛和呼吸困难等非特异性症状。诊断性影像学检查显示存在前纵隔肿块,所有患者均行手术切除。组织学上,所有肿瘤均无包膜,具有不同的生长方式,包括黏液性、非黏液性和乳头状特征。大多数病例表现为混合生长模式,肿瘤局限于纵隔,少数病例延伸至淋巴结或心包。在 2 例中,腺癌与胸腺瘤相关。进行了免疫组织化学染色,其阳性染色根据肿瘤的组织学而有所不同,在一些病例中,角蛋白 7、角蛋白 20、CEA、CD5、CD117 和 CDX-2 呈阳性染色。所有肿瘤均为 PAX8 和 TTF-1 阴性。对 10 例患者进行了 1 至 12 年的随访,结果表明 3 例患者在 14 个月内死亡,1 例发生脑转移,7 例患者存活且无复发。本文所描述的病例涵盖了胸腺上皮肿瘤的范围,并强调了认识这种特殊类型的癌的重要性,因为它可能具有不同的结局并需要不同的治疗选择。

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