Sredni Simone Treiger, da Cunha Isabela Werneck, de Carvalho Filho Nevigolino Pereira, Magrin Jose, Pinto Clovis Antonio Lopes, Lopes Luis Fernando
Department of Pathology, Hospital do Cancer, Rua Professor Antonio Prudente 211, São Paulo 01 509-900, Brazil.
Pediatr Dev Pathol. 2004 Jan-Feb;7(1):77-80. doi: 10.1007/s10024-003-4048-8.
We report a case of a 16-month-old girl with a primary endodermal sinus tumor (EST) of the parotid gland. The girl was admitted to the hospital with a left side cervical tumor with a quick growth (within 3 wk). The tumor was surgically resected. The gross examination showed a 7.0-cm hemorrhagic and fragmentized mass. Diagnosis of an EST was established on the hematoxylin and eosin-stained slides from the resected material. Elevated serum alpha-fetoprotein (AFP) levels were detected and follow-up examinations of the patient did not show ESTs in other locations or other manifestations due to the tumor. The patient received chemotherapy after the surgery and remained alive without evidence of disease at the time of this writing (2 years after the diagnosis). As far as we know, this is the second report in the literature of a parotid gland's EST.
我们报告一例16个月大的女孩,患有腮腺原发性内胚窦瘤(EST)。该女孩因左侧颈部肿瘤快速生长(3周内)入院。肿瘤经手术切除。大体检查显示一个7.0厘米的出血性碎块肿物。通过对切除组织苏木精-伊红染色切片进行检查,确诊为内胚窦瘤。检测到血清甲胎蛋白(AFP)水平升高,对该患者的后续检查未发现其他部位存在EST或该肿瘤的其他表现。患者术后接受了化疗,在撰写本文时(诊断后2年)仍存活且无疾病迹象。据我们所知,这是文献中关于腮腺EST的第二篇报道。