An Hyeong Rok, Cho Kyung-Ja, Song Sang Woo, Park Ji Eun, Song Joon Seon
Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Department of Neurosurgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
J Pathol Transl Med. 2024 Sep;58(5):255-260. doi: 10.4132/jptm.2024.08.15. Epub 2024 Sep 5.
Rhabdomyosarcoma (RMS) comprises of heterogeneous group of neoplasms that occasionally express epithelial markers on immunohistochemistry (IHC). We herein report the case of a patient who developed RMS of the skull with EWSR1 fusion and anaplastic lymphoma kinase (ALK) and cytokeratin expression as cytomorphologic features. A 40-year-old man presented with a mass in his forehead. Surgical resection was performed, during which intraoperative frozen specimens were obtained. Squash cytology showed scattered or clustered spindle and epithelioid cells. IHC revealed that the resected tumor cells were positive for desmin, MyoD1, cytokeratin AE1/ AE3, and ALK. Although EWSR1 rearrangement was identified on fluorescence in situ hybridization, ALK, and TFCP2 rearrangement were not noted. Despite providing adjuvant chemoradiation therapy, the patient died of tumor progression 10 months after diagnosis. We emphasize that a subset of RMS can express cytokeratin and show characteristic histomorphology, implying the need for specific molecular examination.
横纹肌肉瘤(RMS)是一组异质性肿瘤,在免疫组织化学(IHC)中偶尔会表达上皮标志物。我们在此报告一例发生颅骨的RMS患者,其具有EWSR1融合以及间变性淋巴瘤激酶(ALK)和细胞角蛋白表达等细胞形态学特征。一名40岁男性因前额肿物就诊。进行了手术切除,术中获取了冰冻标本。压片细胞学显示散在或聚集的梭形和上皮样细胞。免疫组化显示切除的肿瘤细胞结蛋白、MyoD1、细胞角蛋白AE1/AE3和ALK呈阳性。虽然荧光原位杂交检测到EWSR1重排,但未发现ALK和TFCP2重排。尽管给予了辅助放化疗,患者在诊断后10个月因肿瘤进展死亡。我们强调,一部分RMS可表达细胞角蛋白并表现出特征性组织形态学,这意味着需要进行特定的分子检查。