From the Division of Nuclear Medicine, Department of Radiology (G.A., F.B.), and Division of Dermatology, Department of Medicine (T.A., K.L., P.N.), University of Washington, 1959 NE Pacific St, Box 356113, Seattle, WA 98195-6113; and Department of Radiology, Virginia Commonwealth University Health System, Richmond, Va (S.A.F.).
Radiographics. 2019 Nov-Dec;39(7):2069-2084. doi: 10.1148/rg.2019190102.
Merkel cell carcinoma (MCC) is a rare and aggressive cutaneous neuroendocrine tumor with a higher mortality rate than melanoma. Approximately 40% of MCC patients have nodal or distant metastasis at initial presentation, and one-third of patients will develop distant metastatic disease over their clinical course. Although MCC is rare, its incidence has been steadily increasing. Furthermore, the immunogenicity of MCC and its diagnostic and therapeutic application have made MCC one of the most rapidly developing topics in dermatology and oncology. Owing to the aggressive and complex nature of MCC, a multidisciplinary approach is necessary for management of this tumor, including dermatologists, surgeons, radiation oncologists, medical oncologists, pathologists, radiologists, and nuclear medicine physicians. Imaging plays a crucial role in diagnosis, planning for surgery or radiation therapy, and assessment of treatment response and surveillance. However, MCC is still not well recognized among radiologists and nuclear medicine physicians, likely owing to its rarity. The purpose of this review is to raise awareness of MCC among imaging experts by describing the epidemiology, pathophysiology, and clinical features of MCC and current clinical management with a focus on the role of imaging. The authors highlight imaging findings characteristic of MCC, as well as the clinical significance of CT, MRI, sentinel lymph node mapping, fluorine 18 fluorodeoxyglucose PET/CT, and other nuclear medicine studies such as bone scintigraphy and somatostatin receptor scintigraphy. RSNA, 2019.
默克尔细胞癌(Merkel cell carcinoma,MCC)是一种罕见且侵袭性的皮肤神经内分泌肿瘤,其死亡率高于黑色素瘤。约 40%的 MCC 患者在初始表现时存在淋巴结或远处转移,三分之一的患者在临床过程中会发生远处转移性疾病。尽管 MCC 较为罕见,但其发病率一直在稳步上升。此外,MCC 的免疫原性及其诊断和治疗应用使 MCC 成为皮肤科和肿瘤学中发展最快的课题之一。由于 MCC 的侵袭性和复杂性,需要多学科方法来管理这种肿瘤,包括皮肤科医生、外科医生、放射肿瘤学家、肿瘤内科医生、病理学家、放射科医生和核医学医生。影像学在诊断、手术或放射治疗计划以及评估治疗反应和监测方面发挥着至关重要的作用。然而,由于 MCC 较为罕见,放射科医生和核医学医生对其认识不足。本文旨在通过描述 MCC 的流行病学、病理生理学和临床特征以及当前的临床管理,重点介绍影像学的作用,来提高影像学专家对 MCC 的认识。作者强调了 MCC 的影像学特征,以及 CT、MRI、前哨淋巴结绘图、氟-18 氟代脱氧葡萄糖 PET/CT 以及其他核医学研究(如骨闪烁显像和生长抑素受体闪烁显像)的临床意义。RSNA,2019 年。