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肺低级别纤维黏液样肉瘤:一例报告。

Low-grade fibromyxoid sarcoma arising from the lung: A case report.

机构信息

Department of Thoracic Surgery, Iwate Medical University School of Medicine, Iwate, Japan.

Department of Molecular Diagnostic Pathology, Iwate Medical University School of Medicine, Iwate, Japan.

出版信息

Thorac Cancer. 2021 Sep;12(18):2517-2520. doi: 10.1111/1759-7714.14107. Epub 2021 Aug 10.

Abstract

Low-grade fibromyxoid sarcoma (LGFMS) is a rare sarcoma subtype that most commonly arises in young adults. This tumor typically presents in the deep soft tissues of the proximal extremities or trunk as a painless mass. Although the most common site of LGFMS metastasis is the lung, it is rarely the primary site. Here, we report a case of primary pulmonary LGFMS. A 22-year-old asymptomatic man was referred to our hospital for investigation of a lung mass that had been discovered incidentally. Computed tomography (CT) showed a well-defined mass 4.0 cm in diameter in the upper lobe of the right lung. Malignancy was suggested by focal uptake of 18F-fluorodeoxyglucose positron-emission tomography (18-FDG-PET). Following surgery, postoperative histological analysis of the resected specimen demonstrated LGFMS based on histological and immunohistological findings. In particular, mucin 4 showed diffuse positivity in the spindle-shaped tumor cells. In conclusion, LGFMS can arise in the lungs, and physicians should consider this entity as a differential diagnosis for solitary lung mass in young adults.

摘要

低度纤维黏液样肉瘤(LGFMS)是一种罕见的肉瘤亚型,多见于年轻成年人。该肿瘤通常表现为无痛性肿块,位于四肢近端或躯干的深部软组织中。虽然 LGFMS 转移的最常见部位是肺部,但它很少是原发性部位。在这里,我们报告了一例原发性肺 LGFMS。一名 22 岁无症状男性因偶然发现肺部肿块而被转诊至我院。计算机断层扫描(CT)显示右肺上叶直径 4.0cm 的边界清楚的肿块。18F-氟脱氧葡萄糖正电子发射断层扫描(18-FDG-PET)显示局部摄取提示恶性肿瘤。手术后,对切除标本的术后组织学分析显示,根据组织学和免疫组织化学发现为 LGFMS。特别是,黏液素 4 在梭形肿瘤细胞中呈弥漫性阳性。总之,LGFMS 可发生在肺部,医生应将其作为年轻成人孤立性肺肿块的鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c4a/8447909/c3e3a53af38e/TCA-12-2517-g004.jpg

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