Rajabally Yusuf A, Qaddoura Bassel, Abbott Richard J
Neuromuscular Clinic, Department of Neurology, University Hospitals of Leicester, Leicester, UK.
J Clin Neuromuscul Dis. 2008 Dec;10(2):65-9. doi: 10.1097/CND.0b013e31818e952b.
Paraneoplastic myeloneuropathy has rarely been reported with breast cancer. We report the case of a 59-year-old woman who presented with a peripheral neuropathy and cranial involvement and later developed a myelopathy. The neuropathy was found to be electrophysiologically and histologically demyelinating in nature. Magnetic resonance imaging studies failed to identify any structural brain or spinal cord abnormalities. The patient was diagnosed with breast carcinoma 4 months after initial presentation and underwent resective surgery, radiotherapy, and hormonotherapy. Paraneoplastic antibodies (anti-Hu, anti-Yo, anti-Ri, anti-CV2, anti-Ma, and anti-amphiphysin) were all negative. Her condition did not progress further after cancer treatment. Partial neurologic improvement occurred with oral steroid therapy, with subsequent deterioration on treatment withdrawal.
副肿瘤性脊髓神经病在乳腺癌中鲜有报道。我们报告一例59岁女性,该患者最初表现为周围神经病和颅神经受累,随后发展为脊髓病。经电生理和组织学检查发现,该神经病本质上为脱髓鞘性。磁共振成像检查未发现任何脑部或脊髓结构异常。患者在初次就诊4个月后被诊断为乳腺癌,并接受了切除手术、放疗和激素治疗。副肿瘤抗体(抗Hu、抗Yo、抗Ri、抗CV2、抗Ma和抗 amphiphysin)均为阴性。癌症治疗后她的病情未进一步进展。口服类固醇治疗后神经功能有部分改善,但停药后病情恶化。