Martins Lisandra, Galvão Diogo, Silva Anaísa, Vieira Bárbara, Reis Óscar, Vitorino Rita, Pires Paula
Department of Surgery, Hospital de Santo Espírito da Ilha Terceira, Angra do Heroísmo 9700, Portugal.
Department of Medical Oncology, Hospital de Santo Espírito da Ilha Terceira, Angra do Heroísmo 9700, Portugal.
J Surg Case Rep. 2019 Feb 8;2019(2):rjy365. doi: 10.1093/jscr/rjy365. eCollection 2019 Feb.
Opsoclonus-myoclonus paraneoplastic syndrome is a medical condition that includes opsoclonus along with diffuse or focal body myoclonus and truncal titubation with or without ataxia and other cerebellar signs. This rare neurological syndrome is poorly understood and can result in long-term cognitive, behavioral and motor sequelae. We report a case of a 49-year-old woman with anti-Ri antibody opsoclonus-myoclonus syndrome and an invasive ductal carcinoma with axillary nodes involvement. Following the diagnosis of opsoclonus-myoclonus syndrome, a multimodal immunotherapy treatment, with partial remission of the neurological symptoms. The patient underwent lumpectomy and axillary node dissection and the surgical pathology confirmed the diagnosis of breast cancer stage IIA. This was followed by chemotherapy, radiotherapy and hormone therapy with tamoxifen. At the 6 months follow-up there was a partial improvement, anti-Ri antibody was subsequently reported as negative and there was no evidence of disease recurrence.
眼阵挛-肌阵挛副肿瘤综合征是一种病症,包括眼阵挛以及弥漫性或局灶性身体肌阵挛和躯干震颤,伴有或不伴有共济失调及其他小脑体征。这种罕见的神经综合征了解甚少,可导致长期的认知、行为和运动后遗症。我们报告一例49岁女性,患有抗Ri抗体眼阵挛-肌阵挛综合征及伴有腋窝淋巴结受累的浸润性导管癌。在诊断为眼阵挛-肌阵挛综合征后,采用多模式免疫治疗,神经症状部分缓解。患者接受了肿块切除术和腋窝淋巴结清扫术,手术病理证实为IIA期乳腺癌。随后进行了化疗、放疗和他莫昔芬激素治疗。在6个月的随访中病情有部分改善,抗Ri抗体随后报告为阴性,且无疾病复发迹象。