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[Lipofibroadenoma of the thymus].[胸腺脂肪纤维腺瘤]
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本文引用的文献

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Thymoma: inter-relationships among World Health Organization histology, Masaoka staging and myasthenia gravis and their independent prognostic significance: a single-centre experience.胸腺瘤:世界卫生组织组织学分型、Masaoka 分期、重症肌无力之间的相互关系及其独立的预后意义:单中心经验。
Eur J Cardiothorac Surg. 2011 Jul;40(1):146-53. doi: 10.1016/j.ejcts.2010.09.042. Epub 2010 Nov 18.
2
Type B thymoma: is prognosis predicted only by World Health Organization classification?B 型胸腺瘤:预后仅能由世界卫生组织分类预测吗?
J Thorac Cardiovasc Surg. 2010 Jun;139(6):1431-1435.e1. doi: 10.1016/j.jtcvs.2009.10.024. Epub 2009 Dec 28.
3
[Thymoma associated with an lipofibroadenoma: report of a case].[胸腺瘤合并脂肪纤维腺瘤:1例报告]
Zhonghua Bing Li Xue Za Zhi. 2009 Aug;38(8):556-7.
4
[Lipofibroadenoma of the thymus].[胸腺脂肪纤维腺瘤]
Kyobu Geka. 2009 May;62(5):395-8.
5
Correlation of the WHO schema for the classification of thymic epithelial neoplasms with prognosis: a retrospective study of 90 tumors.世界卫生组织胸腺上皮肿瘤分类方案与预后的相关性:90例肿瘤的回顾性研究
Am J Surg Pathol. 2002 Dec;26(12):1605-11. doi: 10.1097/00000478-200212000-00008.
6
The World Health Organization histologic classification system reflects the oncologic behavior of thymoma: a clinical study of 273 patients.世界卫生组织组织学分类系统反映胸腺瘤的肿瘤行为:273例患者的临床研究
Cancer. 2002 Feb 1;94(3):624-32. doi: 10.1002/cncr.10226.
7
Histologic types of thymoma associated with pure red cell aplasia: a study of five cases including a composite tumor of organoid thymoma associated with an unusual lipofibroadenoma.与纯红细胞再生障碍相关的胸腺瘤组织学类型:一项包括类器官胸腺瘤与罕见脂肪纤维腺瘤复合肿瘤的5例病例研究。
Int J Surg Pathol. 2001 Jan;9(1):29-35. doi: 10.1177/106689690100900106.
8
[Ultrasound-guided biopsies for breast nodules: value of automatic biopsy needle].超声引导下乳腺结节活检:自动活检针的价值
Contracept Fertil Sex. 1996 May;24(5):399-406.
9
Pulmonary and pleural thymoma. Diagnostic application of lymphocyte markers to the thymoma of unusual site.肺及胸膜胸腺瘤。淋巴细胞标志物在罕见部位胸腺瘤诊断中的应用。
Am J Clin Pathol. 1988 May;89(5):617-21. doi: 10.1093/ajcp/89.5.617.

一种表现为巨大胸内肿瘤的罕见胸腺瘤类型:脂肪纤维腺瘤。

A rare thymoma type presenting as a giant intrathoracic tumor: lipofibroadenoma.

作者信息

Aydin Yener, Sipal Sare, Celik Mine, Araz Omer, Ulas Ali Bilal, Alper Fatih, Eroglu Atila

机构信息

Department of Thoracic Surgery, Faculty of Medicine, Ataturk University, Erzurum, Turkey.

Department of Pathology, Faculty of Medicine, Ataturk University, Erzurum, Turkey.

出版信息

Eurasian J Med. 2012 Dec;44(3):176-8. doi: 10.5152/eajm.2012.41.

DOI:10.5152/eajm.2012.41
PMID:25610236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4261387/
Abstract

Type B1 thymoma (lipofibroadenoma) is extremely rare. The tumor is characterized by an organoid appearance rich in lymphocytes with medullary differentiation and perivascular spaces. A twenty-three-year-old female patient was admitted to our clinic with complaints of chest pain and dyspnea for six months. Chest computed tomography showed solid and fatty components of masses 21×7 and 5×7 cm with clear borders in the right thoracic cavity. The patient underwent a posterolateral thoracotomy in which the mass, arising from the anterior mediastinum, was resected. Histopathological examination showed that the mass was Type B1 thymoma, and the patient was presented in light of the literature.

摘要

B1型胸腺瘤(脂肪纤维腺瘤)极为罕见。该肿瘤的特征是呈类器官外观,富含具有髓质分化的淋巴细胞和血管周围间隙。一名23岁女性患者因胸痛和呼吸困难6个月前来我院就诊。胸部计算机断层扫描显示右胸腔内有边界清晰的21×7 cm和5×7 cm肿块,包含实性和脂肪成分。患者接受了后外侧开胸手术,切除了起源于前纵隔的肿块。组织病理学检查显示该肿块为B1型胸腺瘤,并结合文献对该患者进行了介绍。