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腹壁硬纤维瘤既往切除术后13年出现多个肺结节的胸腔内硬纤维瘤

Intrathoracic Desmoid Tumor Presenting as Multiple Lung Nodules 13 Years after Previous Resection of Abdominal Wall Desmoid Tumor.

作者信息

Koo Gun Woo, Chung Sung Jun, Kwak Joo Hee, Oh Chang Kyo, Park Dong Won, Kwak Hyeon Jung, Moon Ji-Yong, Kim Sang-Heon, Sohn Jang Won, Yoon Ho Joo, Shin Dong Ho, Park Sung Soo, Oh Young-Ha, Pyo Ju Yeon, Kim Tae-Hyung

机构信息

Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea.

Department of Pathology, Hanyang University College of Medicine, Seoul, Korea.

出版信息

Tuberc Respir Dis (Seoul). 2015 Jul;78(3):267-71. doi: 10.4046/trd.2015.78.3.267. Epub 2015 Jun 30.

Abstract

Desmoid tumors are rare soft tissue tumors considered to have locally infiltrative features without distant metastasis until now. Although they are most commonly intraabdominal, very few cases have extra-abdominal locations. The origin of intrathoracic desmoid tumors is predominantly the chest wall with occasional involvement of pleura. True intrathoracic primary desmoid tumors with no involvement of the chest wall or pleura are extremely rare. We recently experienced a case of true intrathoracic desmoid tumor presenting as multiple lung nodules at 13 years after resection of a previous intraabdominal desmoid tumor.

摘要

硬纤维瘤是一种罕见的软组织肿瘤,迄今为止被认为具有局部浸润性特征且无远处转移。虽然它们最常见于腹腔内,但极少有位于腹腔外的病例。胸内硬纤维瘤主要起源于胸壁,偶尔累及胸膜。真正的胸内原发性硬纤维瘤且不累及胸壁或胸膜极为罕见。我们最近遇到一例真正的胸内硬纤维瘤病例,该病例在先前腹腔内硬纤维瘤切除术后13年表现为多发肺结节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e65/4499597/2977a2fff504/trd-78-267-g001.jpg

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