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胸腺黏液腺癌:胸腺癌的一种独特亚型。

Mucinous adenocarcinoma of the thymus: a distinct variant of thymic carcinoma.

作者信息

Maeda Daichi, Ota Satoshi, Ikeda Shingo, Kawano Ryoji, Hata Enjo, Nakajima Jun, Mori Masaya, Fukayama Masashi

机构信息

Department of Pathology, Mitsui Memorial Hospital, 1 Kandaizumicho Chiyodaku, Tokyo, Japan.

出版信息

Lung Cancer. 2009 Apr;64(1):22-7. doi: 10.1016/j.lungcan.2008.06.019. Epub 2008 Aug 22.

Abstract

BACKGROUND

Primary thymic mucinous adenocarcinoma is a recently described subtype of thymic carcinoma, which behaves aggressively.

METHODS

The authors analyzed the clinical and pathological findings of three cases of thymic mucinous adenocarcinoma, and reviewed five cases previously reported in the English literature.

RESULTS

The patients were two males and one female between the ages of 38 and 55 years. Macroscopically, the tumors were mostly solid and white to yellowish-white. Areas with a gelatinous appearance were present. Histologically, all of the tumors were adenocarcinomas with abundant mucin production, which resembled the mucinous adenocarcinomas of other organs. Malignant tumor cells in nests, tubules and cribriform structures floated in pools of extracellular mucin. In one case, associated thymic cysts were found at the periphery of the tumor. The cyst wall was partially lined by malignant mucinous epithelium, which showed transition from benign thymic epithelium. Immunohistochemically, all of the tumors showed positive immunoreactivity for cytokeratin (CK) 20 and carcinoembryonic antigen (CEA). CD5 was diffusely positive in one case, and focally positive in the other two cases. The prognoses of these cases were extremely poor, and two of the patients died within 24 months.

CONCLUSION

Growing evidence suggests that mucinous adenocarcinoma is a distinct morphological variant of primary thymic carcinoma. We believe that clinicians and surgical pathologists should include thymic mucinous adenocarcinoma in the differential diagnosis of mediastinal adenocarcinoma.

摘要

背景

原发性胸腺黏液腺癌是最近描述的一种胸腺癌亚型,其行为具有侵袭性。

方法

作者分析了3例胸腺黏液腺癌的临床和病理表现,并复习了英文文献中先前报道的5例病例。

结果

患者为2名男性和1名女性,年龄在38至55岁之间。大体上,肿瘤大多为实性,呈白色至黄白色。存在外观呈胶冻状的区域。组织学上,所有肿瘤均为腺癌,伴有大量黏液产生,类似于其他器官的黏液腺癌。巢状、小管状和筛状结构中的恶性肿瘤细胞漂浮在细胞外黏液池中。1例病例中,在肿瘤周边发现了相关的胸腺囊肿。囊肿壁部分内衬恶性黏液上皮,显示出从良性胸腺上皮的转变。免疫组化方面,所有肿瘤对细胞角蛋白(CK)20和癌胚抗原(CEA)均呈阳性免疫反应。1例病例中CD5弥漫性阳性,另外2例病例中呈局灶性阳性。这些病例的预后极差,2例患者在24个月内死亡。

结论

越来越多的证据表明黏液腺癌是原发性胸腺癌的一种独特形态学变异。我们认为临床医生和外科病理学家在纵隔腺癌的鉴别诊断中应考虑胸腺黏液腺癌。

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