Negru Maria Emanuela, Sponghini Andrea Pietro, Rondonotti David, Platini Francesca, Giavarra Marco, Forti Laura, Lombardi Mariangela, Masini Laura, Boldorini Renzo, Galetto Alessandra
Medical Oncology Unit, School of Medicine, University Hospital Maggiore della Carità, I-28100 Novara, Italy.
Radiodiagnostic and Interventional Radiology Institute, School of Medicine, University Hospital Maggiore della Carità, I-28100 Novara, Italy.
Mol Clin Oncol. 2015 Jul;3(4):807-810. doi: 10.3892/mco.2015.548. Epub 2015 Apr 24.
Ewing's sarcoma (ES) is an aggressive tumour that may present with skeletal and extraskeletal forms. The extraskeletal form is rarely encountered in the head and neck region and is extremely rare in the sinonasal tract. This is the case report of a ES of the ethmoid sinus with intracranial and orbital extension in a 33-year-old male patient who presented with anosmia, epistaxis, reduction of visual acuity in the left eye and headache. On otorhinolaryngological clinical examination and biopsy via flexible endoscope, the lesion was misdiagnosed as ethmoid sinus carcinoma. The subsequent magnetic resonance imaging (MRI) of the brain revealed a large mass (6×7 cm) eroding the ethmoid and sphenoid sinuses, extending beyond the orbits and occupying the anterior cranial fossa with a maximum extension of ~5 cm. The patient underwent surgical resection and the microscopic examination of the specimen established the diagnosis of ES (immunohistochemically positive for CD99, neuron-specific enolase, CD56, synaptophysin, pancytokeratin, low-molecular weight cytokeratins and vimentin. The periodic acid Schiff stain exhibited strong intracytoplasmic block positivity and fluorescence hybridization revealed a t(22;11) translocation. First-line chemotherapy was administered for 3 cycles; however, on restaging MRI, local disease progression was diagnosed. The patient received radiotherapy and second-line chemotherapy for 6 cycles. At 15 months after the diagnosis, the patient remains recurrence-free and maintains a good functional status and quality of life.
尤因肉瘤(ES)是一种侵袭性肿瘤,可表现为骨骼和骨骼外形式。骨骼外形式在头颈部区域很少见,在鼻窦中极为罕见。本文报告一例33岁男性患者,其筛窦ES伴有颅内和眶内扩展,表现为嗅觉减退、鼻出血、左眼视力下降和头痛。经耳鼻咽喉科临床检查及柔性内镜活检,该病变被误诊为筛窦癌。随后的脑部磁共振成像(MRI)显示一个大肿块(6×7 cm),侵蚀筛窦和蝶窦,超出眼眶范围,占据前颅窝,最大扩展约5 cm。患者接受了手术切除,标本的显微镜检查确诊为ES(免疫组化CD99、神经元特异性烯醇化酶、CD56、突触素、全细胞角蛋白、低分子量细胞角蛋白和波形蛋白均为阳性。过碘酸希夫染色显示强细胞质内块状阳性,荧光杂交显示t(22;11)易位。给予一线化疗3个周期;然而,在重新分期的MRI上,诊断为局部疾病进展。患者接受了放疗和二线化疗6个周期。诊断后15个月,患者无复发,功能状态和生活质量良好。