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肺颗粒细胞瘤:病例报告及文献综述

Pulmonary granular cell tumours: case presentations and literature review.

作者信息

Radić Petra, Brčić Luka

机构信息

1 Consultant Pathologist (staff member), Institute of Pathology, School of Medicine, University of Zagreb, Croatia.

2 Trainee (resident), Institute of Pathology, Medical University of Graz, Austria.

出版信息

Scott Med J. 2017 May;62(2):70-73. doi: 10.1177/0036933017711796. Epub 2017 May 23.

Abstract

Pulmonary granular cells tumours are very rare tumours, most probably originating from Schwann cells. Although rare, clinical and biological presentation is diverse. They are most commonly endobronchial masses, usually a solitary pulmonary lesion, although in up to 20% they can occur as multiple lesions and can be mistaken for malignant process. In spite of infiltrative growth, and rare direct lymph node invasion, they have a very good prognosis if completely removed. Here we present two cases from the archives of the Institute of Pathology, University of Zagreb School of Medicine, with literature review.

摘要

肺颗粒细胞瘤是非常罕见的肿瘤,很可能起源于施万细胞。尽管罕见,但其临床和生物学表现多样。它们最常见于支气管内肿物,通常为孤立性肺病变,不过高达20%的病例可表现为多发病变,并且可能被误诊为恶性病变。尽管呈浸润性生长,且罕见直接侵犯淋巴结,但如果能完全切除,其预后非常好。在此,我们展示萨格勒布大学医学院病理学研究所存档的两例病例,并进行文献综述。

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