Jaramillo Couger Jimenez, Wojcik John, Weber Kristy, Sebro Ronnie
Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Pathology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Oncol Lett. 2018 Apr;15(4):4720-4730. doi: 10.3892/ol.2018.7929. Epub 2018 Feb 2.
Pleomorphic hyalinizing angiectatic tumors (PHATs) are rare mesenchymal soft tissue tumors of uncertain lineage and intermediate malignancy. The present study assesses two cases of PHAT and discusses the histological and immunophenotypical features, as well as the imaging appearance of these tumors on ultrasound, computed tomography (CT), magnetic resonance imaging and positron emission tomography/CT scans. The current study also reviews the literature and discusses the clinical management of these tumors. Wide local excision with tumor free margins is the current recommended treatment for PHAT. Surgical excision may be combined with low-dose radiation to reduce the risk of local recurrence. Patients should be followed up with serial imaging, as PHAT lesions tend to recur locally.
多形性透明变性血管扩张性肿瘤(PHATs)是一种罕见的间叶性软组织肿瘤,其谱系不确定,恶性程度为中等。本研究评估了两例PHAT病例,并讨论了这些肿瘤的组织学和免疫表型特征,以及它们在超声、计算机断层扫描(CT)、磁共振成像和正电子发射断层扫描/CT扫描上的影像学表现。本研究还回顾了文献,并讨论了这些肿瘤的临床管理。目前推荐对PHAT进行切缘无肿瘤的广泛局部切除治疗。手术切除可联合低剂量放疗以降低局部复发风险。由于PHAT病变往往会局部复发,因此应对患者进行系列影像学随访。