中国现代神经疾病杂志 ›› 2018, Vol. 18 ›› Issue (7): 535-539. doi: 10.3969/j.issn.1672-6731.2018.07.011

• 临床研究 • 上一篇    下一篇

2 以中枢神经系统和周围神经系统损害为临床表现的多发对称性脂肪瘤病一例并文献复习

姜季委, 商秀丽   

  1. 110001 沈阳,中国医科大学附属第一医院神经内科
  • 出版日期:2018-07-25 发布日期:2018-08-02
  • 通讯作者: 商秀丽(Email:shang_zhao@sohu.com)
  • 基金资助:

    国家自然科学基金青年科学基金资助项目(项目编号:81100243);国家自然科学基金青年科学基金资助项目(项目编号:81502181);辽宁省重点研发计划指导计划项目(项目编号:2017225027);辽宁省沈阳市科技计划项目(项目编号:17-230-9-17)

Central and peripheral neuropathy as the manifestations of multiple symmetric lipomatosis: one case report and review of literatures

JIANG Ji-wei, SHANG Xiu-li   

  1. Department of Neurology, the First Hospital of China Medical University, Shenyang 110001, Liaoning, China
  • Online:2018-07-25 Published:2018-08-02
  • Contact: SHANG Xiu-li (Email: shang_zhao@sohu.com)
  • Supported by:

    This study was supported by the National Natural Science Foundation for Young Scientists of China (No. 81100243, 81502181), Guidance Fund of Key Research and Development Plan in Liaoning Province, China (No. 2017225027), and Technology Fund of Shenyang, Liaoning Province, China (No. 17-230-9-17).

摘要:

目的 总结多发对称性脂肪瘤病合并中枢神经系统和周围神经系统损害的临床和影像学特点,并探讨其发病机制。方法与结果 男性患者,66 岁,临床表现为双侧颌下部、颈部、肩部和上背部对称性无痛性脂肪团块2 年,双下肢麻木无力6 个月,反应迟钝、胡言乱语、右侧足底无痛性溃疡15 d。神经系统查体近记忆力、计算力和理解力下降,双侧锥体束征,右膝以下痛温觉消失、位置觉和震动觉减退。颈椎MRI 可见双侧颈部对称性且无包膜的脂肪团块影;头部MRI 未见明显异常。临床诊断为多发对称性脂肪瘤病合并中枢神经系统和周围神经系统损害。嘱患者戒酒,予甲钴胺、腺苷钴胺、叶酸、复方二氯醋酸二异丙胺、瑞舒伐他汀综合治疗。共住院14 d,随访3 个月,症状部分消失。结论 多发对称性脂肪瘤病是罕见的脂肪代谢障碍性疾病,可以合并中枢神经系统和周围神经系统损害,其发病机制尚待进一步研究。

关键词: 脂肪瘤样病, 多发性对称性, 中枢神经系统, 周围神经系统, 磁共振成像

Abstract:

Objective To summarize the clinical manifestations and imaging features of multiple symmetric lipomatosis (MSL) combined with central and peripheral neuropathy, and to explore its pathogenesis. Methods and Results We reported a 66-year-old man with long-term history of alcoholism. Several large symmetric and painless lipomas were found in his bilateral lower jaw, shoulders, neck and upper back over the past 2 years. The patient suffered from numbness and weakness of both lower extremities for 6 months, and sudden dullness, balderdash, even painless ulcer in the right sole for 15 d. Neurologic examination showed that his recent memory, calculation and understanding ability were decreased, and it appeared bilateral pyramidal tract syndrome and ataxia. The algesia and thermesthesia below the right knee were lost, and topesthesia and pallesthesia were decreased. Cervical MRI showed cervical subcutaneous symmetric and non-encapsulated fat-intense mass. No significant abnormality was found in brain MRI. It was eventually diagnosed with MSL combined with central and peripheral neuropathy. The treatment included oral mecobalamine, cobamamide, folate, compound diisopropylamine dichloroacetate, rosuvastatin, and abstaining from alcohol. The patient was hospitalized for 14 d and followed up for 3 months, and the symptoms disappeared partially. Conclusions MSL is a rare disease with abnormal fat metabolism, which can result in both central and peripheral neuropathy. The pathogenesis of MSL, especially the cause of brain damage in MSL needs to be further explored.

Key words: Lipomatosis, multiple symmetrial, Central nervous system, Peripheral nervous system, Magnetic resonance imaging