Cruzado-Sánchez Deivy, Salas-Diaz Sandra, Tellez Walter A, Maquera-Torres Grisnery, Serpa-Frias Solon
Instituto Nacional de Enfermedades Neoplásicas (INEN). Lima, Perú.
Sociedad Científica de Estudiantes de Medicina Villarrealinos (SOCEMVI), Universidad Nacional Federico Villarreal. Lima, Perú.
Rev Peru Med Exp Salud Publica. 2017 Jul-Sep;34(3):560-563. doi: 10.17843/rpmesp.2017.343.2809.
Primary orbital cystic tumors caused by Echinococcus granulosus are rare. As this parasite is endemic in Peru, we report the case of a 10-year-old girl from a rural area of Huancavelica, who presented with progressive and irreducible axial proptosis of the right eye and loss of vision. Orbital tomographic images demonstrated a tumor mass with a cystic appearance. Serologic tests were negative. The patient underwent surgical resection, and histopathologic analysis revealed anhistic membranes, corresponding to hydatid cysts. During one year of follow-up, no evidence of local or systemic recurrence was observed. In conclusion, orbital hydatidosis should be considered in the differential diagnosis of a cystic orbital tumor in pediatric patients, especially if the patient is from an endemic area.
由细粒棘球绦虫引起的原发性眼眶囊性肿瘤很罕见。由于这种寄生虫在秘鲁为地方病,我们报告了一名来自万卡韦利卡农村地区的10岁女孩的病例,她出现右眼进行性且不可复位的轴向眼球突出和视力丧失。眼眶断层图像显示一个具有囊性外观的肿瘤块。血清学检查为阴性。患者接受了手术切除,组织病理学分析显示无组织结构的膜,符合包虫囊肿。在一年的随访中,未观察到局部或全身复发的迹象。总之,在小儿患者眼眶囊性肿瘤的鉴别诊断中应考虑眼眶包虫病,特别是如果患者来自地方病流行地区。