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一种罕见的肺错构瘤:纤维平滑肌瘤性错构瘤。

A rare pulmonary hamartoma: fibroleiomyomatous hamartoma.

作者信息

Ichiki Yoshinobu, Kawasaki Junji, Hamatsu Takayuki, Suehiro Taketoshi, Shibuya Ryo, Matsuyama Atsuji, Tanaka Fumihiro, Hisaoka Masanori, Sugimachi Keizo

机构信息

Department of Chest Surgery, Onga Nakama Medical Association Onga Hospital, 1725-2 Ooaza-Ozaki Ongacho, Onga-gun, Fukuoka, 811-4342, Japan.

Department of Surgery, Onga Nakama Medical Association Onga Hospital, Onga-gun, Fukuoka, Japan.

出版信息

Surg Case Rep. 2016 Dec;2(1):53. doi: 10.1186/s40792-016-0184-z. Epub 2016 Jun 2.

Abstract

Pulmonary hamartomas are more common than expected because they are usually asymptomatic and are either discovered on routine chest radiography or when they are noted incidentally in approximately 0.25 % of autopsies. In contrast, pulmonary fibroleiomyomatous hamartoma, which consists of interlacing bundles of smooth muscle cells admixed with fibrous tissue and numerous tubular or cleft-like epithelial inclusions, is a rare type of hamartoma. Controversy exists regarding the pathogenesis of this tumor. We herein present a rare case of a 68-year-old male patient without a pre-existing smooth muscle tumor, who underwent resection for a tumor that was considered to be a true pulmonary fibroleiomyomatous hamartoma.

摘要

肺错构瘤比预期更为常见,因为它们通常无症状,要么在常规胸部X线检查时被发现,要么在约0.25%的尸检中偶然被注意到。相比之下,肺纤维平滑肌瘤性错构瘤是一种罕见的错构瘤类型,它由交织的平滑肌细胞束与纤维组织以及许多管状或裂隙样上皮包涵体混合组成。关于这种肿瘤的发病机制存在争议。我们在此报告一例罕见病例,一名68岁男性患者,既往无平滑肌瘤病史,因被认为是真正的肺纤维平滑肌瘤性错构瘤的肿瘤而接受了切除术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e84f/4891308/41b3762bec14/40792_2016_184_Fig1_HTML.jpg

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