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化生性胸腺瘤:4例报告

Metaplastic thymoma: report of 4 cases.

作者信息

Kang Guhyun, Yoon Nara, Han Joungho, Kim Young Eun, Kim Tae Sung, Kim Kwhanmien

机构信息

Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

Korean J Pathol. 2012 Feb;46(1):92-5. doi: 10.4132/KoreanJPathol.2012.46.1.92. Epub 2012 Feb 23.

DOI:10.4132/KoreanJPathol.2012.46.1.92
PMID:23109986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3479700/
Abstract

Metaplastic thymoma (MT), accepted in the World Health Organization 2004 scheme, is a circumscribed tumor of the thymus exhibiting biphasic morphology. We herein describe the clinicopathologic features of four MTs and the differential diagnoses of this unusual tumor. There were three women and one man with mean age of 49.5 years. The patients were found to have mediastinal masses, and underwent surgical excision. One exhibited symptoms of myasthenia gravis, and the serum titer for anti-acetylcholine receptor antibody was positive. Grossly, the tumors were encapsulated, and showed vaguely multinodular, solid, tan-white to yellow cut surfaces. Histologically, they comprised epithelial islands intertwining with bundles of delicate spindle cells. The patients remained well after surgical excision at 5-55 months. Because of the distinctive histological appearance and benign clinical course, MT should be distinguished from other more aggressive mediastinal neoplasms displaying biphasic feature.

摘要

化生性胸腺瘤(MT)在2004年世界卫生组织分类方案中被认可,是一种具有双相形态的胸腺局限性肿瘤。我们在此描述4例MT的临床病理特征以及这种不寻常肿瘤的鉴别诊断。患者有3名女性和1名男性,平均年龄49.5岁。这些患者被发现有纵隔肿块,并接受了手术切除。其中1例表现出重症肌无力症状,抗乙酰胆碱受体抗体血清滴度呈阳性。大体上,肿瘤有包膜,切面呈模糊的多结节状、实性,棕白色至黄色。组织学上,它们由上皮岛与纤细的梭形细胞束相互交织组成。手术切除后,患者在5至55个月内情况良好。由于其独特的组织学表现和良性临床过程,MT应与其他表现出双相特征的更具侵袭性的纵隔肿瘤相鉴别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688e/3479700/f4f33b29dbcc/kjpathol-46-92-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688e/3479700/f4f33b29dbcc/kjpathol-46-92-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/688e/3479700/f4f33b29dbcc/kjpathol-46-92-g001.jpg

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Metaplastic thymoma with myasthenia gravis presumably caused by an accumulation of intratumoral immature T cells: a case report.伴重症肌无力的化生性胸腺瘤可能由肿瘤内不成熟T细胞积聚所致:一例报告
Int J Clin Exp Pathol. 2015 Nov 1;8(11):15375-80. eCollection 2015.
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