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罕见的原发性肺血管肉瘤伴神经内分泌分化异常。

Rare primary pulmonary angiosarcoma with aberrant neuroendocrine differentiation.

机构信息

Department of Radiology, Loyola University Medical Center, 2160 S. 1st Ave., Maywood, IL 60153, United States of America.

Loyola University Stritch School of Medicine, 2160 S. 1st Ave., Maywood, IL 60153, United States of America.

出版信息

Clin Imaging. 2022 Feb;82:88-93. doi: 10.1016/j.clinimag.2021.11.002. Epub 2021 Nov 16.

Abstract

Angiosarcomas are aggressive, malignant endothelial cell tumors derived from the vascular or lymphatic epithelium. Angiosarcomas makes up less than 1% of all soft tissue sarcomas. Primary pulmonary angiosarcoma is a rare tumor that most commonly presents as metastatic disease and carries a grim prognosis. The disease rarity and low index of suspicion make the diagnosis problematic. In this report, we present a case of primary pulmonary angiosarcoma with aberrant neuroendocrine differentiation. The diagnostic images, pathology and management strategy are discussed in this case with overall longer survival. The unique neuroendocrine pathologic subtype may contribute to the overall longer survival, however, there are only a few limited cases published. Further recognition and investigation of primary pulmonary angiosarcoma with aberrant neuroendocrine differentiation is warranted to further characterize diagnostic markers, determine more effective treatment strategies, and establish a possible link to improved survival.

摘要

血管肉瘤是一种侵袭性的、恶性的内皮细胞肿瘤,来源于血管或淋巴管的上皮细胞。血管肉瘤占所有软组织肉瘤的比例不到 1%。原发性肺血管肉瘤是一种罕见的肿瘤,最常表现为转移性疾病,预后不良。由于疾病罕见,且怀疑指数低,导致诊断存在问题。在本报告中,我们介绍了一例具有神经内分泌分化异常的原发性肺血管肉瘤病例。本文讨论了该病例的诊断图像、病理和管理策略,总体生存时间较长。独特的神经内分泌病理亚型可能有助于整体的生存时间延长,但发表的相关病例非常有限。进一步认识和研究具有神经内分泌分化异常的原发性肺血管肉瘤,对于进一步确定诊断标志物、确定更有效的治疗策略以及建立与生存改善相关的可能联系具有重要意义。

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