Li Long, Molberg Kyle, Cheedella Naga, Thibodeaux Joel, Hinson Stacy, Lucas Elena
Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, 75390.
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, 75390.
Diagn Cytopathol. 2018 Jan;46(1):67-71. doi: 10.1002/dc.23794. Epub 2017 Aug 12.
Merkel cell carcinoma (MCC) is an aggressive skin tumor with a high tendency for metastases. We report a case of MCC initially presenting as axillary and pancreatic metastases. A 33-year-old HIV-positive Hispanic male presented with a history of a rapidly growing axillary mass. A needle core biopsy demonstrated an epithelioid neoplasm composed of small to medium-sized cells with high nuclear-cytoplasmic ratio, nuclear molding, and frequent mitotic figures. A subsequent PET scan revealed a 1.5 cm FDG avid mass in the pancreas. Endoscopic ultrasound-guided FNA of the pancreatic mass showed neoplastic cells with similar morphology to those of the axillary mass. The tumor cells were positive with pancytokeratin AE1/AE3, CK20, CD56, synatophysin, chromogranin, and Merkel cell polyomavirus (MCPyV). This case of MCC most likely originated from a resolved primary skin lesion drained by the involved axillary lymph node with subsequent metastases to the pancreas and distant lymph nodes.
默克尔细胞癌(MCC)是一种侵袭性皮肤肿瘤,具有很高的转移倾向。我们报告一例最初表现为腋窝和胰腺转移的MCC病例。一名33岁的HIV阳性西班牙裔男性,有快速生长的腋窝肿块病史。针芯活检显示为上皮样肿瘤,由核质比高、核异型性及频繁核分裂象的中小细胞组成。随后的PET扫描显示胰腺有一个1.5 cm的FDG摄取阳性肿块。胰腺肿块的内镜超声引导下细针穿刺活检显示肿瘤细胞形态与腋窝肿块相似。肿瘤细胞全细胞角蛋白AE1/AE3、CK20、CD56、突触素、嗜铬粒蛋白及默克尔细胞多瘤病毒(MCPyV)均呈阳性。该例MCC很可能起源于已消退的原发性皮肤病变,由受累腋窝淋巴结引流,随后转移至胰腺和远处淋巴结。