发生在后纵隔的有勒氏分枝分化的纤毛囊肿。

Korean Journal of Pathology Pub Date : 2014-10-01 Epub Date: 2014-10-27 DOI:10.4132/KoreanJPathol.2014.48.5.401
So Jung Lee, Chung Su Hwang, Do Youn Park, Gi Young Huh, Chang Hun Lee
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引用次数: 10

摘要

本文章由计算机程序翻译,如有差异,请以英文原文为准。

A ciliated cyst with müllerian differentiation arising in the posterior mediastinum.

A ciliated cyst with müllerian differentiation arising in the posterior mediastinum.

A ciliated cyst with müllerian differentiation arising in the posterior mediastinum.
Primary congenital mediastinal cysts are rare, have a broad range of etiologies, and can be bronchogenic, thymic, neuroenteric, or esophageal in origin[1]. Recently, Hattori[2] described the first case of a ciliated cyst of probable Mullerian origin arising in the posterior mediastinum, a so-called Hattori’s cyst. Since that time, several additional cases have been reported[3,4]. We found a posterior mediastinal cyst with Mullerian differentiation that was consistent with previous description of Hattori’s cyst. To our knowledge, this is the first report of Hattori’s cyst arising in the posterior mediastinum in Korea.
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来源期刊
Korean Journal of Pathology
Korean Journal of Pathology 医学-病理学
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