Charles S, Hainaut E, Cante V, Valette C, Levillain P, Guillet G
Dermatologie, CHU de la Milétrie, 2, rue de la Milétrie, 86021 Poitiers cedex, France.
Dermatologie, CHU de la Milétrie, 2, rue de la Milétrie, 86021 Poitiers cedex, France.
Ann Dermatol Venereol. 2014 Aug-Sep;141(8-9):523-7. doi: 10.1016/j.annder.2014.04.123. Epub 2014 Jun 2.
Dermato-neuro syndrome is a specific neurological complication of scleromyxedema presenting with fever, coma, seizures and flu-like syndrome. To our knowledge, it has only been reported about twenty times in the literature. Its outcome is uncertain. We describe the case of a patient in whom a favorable outcome was achieved using a combination of plasmapheresis and intravenous immunoglobulin (IVIG).
A 57-year-old woman was diagnosed 14 years ago with scleromyxedema resistant to multiple lines of treatment. In November 2011, she presented an initial episode of epileptic seizure followed by post-seizure coma, and later, confusional state with visual hallucinations. She recovered spontaneously within a few days. CT scan, MRI, EEG and screening for infection were perfectly normal, resulting in suspicion of neurological involvement associated with her scleromyxedema. In December 2012 and August 2013, she presented two further episodes of status epilepticus, followed once more by a confusional state, with etiological explorations again proving unfruitful. On this occasion, her confusional state persisted for two months until the initiation of plasmapheresis and IVIG. This combination therapy led to rapid regression of all neurological symptoms and an improvement in her general condition.
The dermato-neuro syndrome is a rare neurological complication of scleromyxedema. Its pathophysiology is unknown. The monoclonal gammopathy induced by the scleromyxedema could account for the patient's hypercoagulable state and for the formation of neutrophilic aggregates leading to impaired microcirculation. Treatment is empirical and poorly codified. The course of the disease is unpredictable and may be lethal.
皮肤神经综合征是硬皮病黏液水肿的一种特殊神经并发症,表现为发热、昏迷、癫痫发作和类流感综合征。据我们所知,其在文献中仅被报道过约20次。其预后尚不确定。我们描述了一例通过血浆置换和静脉注射免疫球蛋白(IVIG)联合治疗取得良好预后的患者病例。
一名57岁女性14年前被诊断为硬皮病黏液水肿,对多种治疗方法均耐药。2011年11月,她首次出现癫痫发作,随后是发作后昏迷,之后出现伴有视幻觉的意识模糊状态。她在几天内自发康复。CT扫描、MRI、脑电图和感染筛查均完全正常,因此怀疑其神经受累与硬皮病黏液水肿有关。2012年12月和2013年8月,她又出现了两次癫痫持续状态,随后再次出现意识模糊状态,病因探索再次无果。此次,她的意识模糊状态持续了两个月,直到开始进行血浆置换和IVIG治疗。这种联合治疗导致所有神经症状迅速消退,她的总体状况得到改善。
皮肤神经综合征是硬皮病黏液水肿一种罕见的神经并发症。其病理生理学尚不清楚。硬皮病黏液水肿诱发的单克隆丙种球蛋白病可能是患者高凝状态的原因,也是导致中性粒细胞聚集形成从而导致微循环受损的原因。治疗是经验性的,且缺乏明确规范。该疾病的病程不可预测,可能是致命的。