Jensen T S, Schrøder H D, Jønsson V, Ernerudh J, Stigsby B, Kamieniecka Z, Hippe E, Trojaborg W
Department of Neurology, Rigshospitalet, University of Copenhagen, Denmark.
J Neurol Neurosurg Psychiatry. 1988 Oct;51(10):1308-15. doi: 10.1136/jnnp.51.10.1308.
A sister and a brother with a progressive mixed axonal and demyelinating polyneuropathy were found to have a monoclonal IgM gammopathy of kappa and lambda type, respectively. Sural nerve and cutaneous nerve specimens obtained by biopsy showed deposits of IgM on myelin sheets. Sera from both patients contained antibodies directed to bovine peripheral nerve myelin as determined by ELISA technique and to normal human peripheral nerve myelin as demonstrated by indirect immunofluorescence histochemistry. These siblings may have a genetic predisposition to the formation of autoantibodies with peripheral nerve myelin as the target for the immune attack.
一名患有进行性混合性轴索性和脱髓鞘性多发性神经病的姐妹和兄弟,分别被发现患有κ型和λ型单克隆IgM丙种球蛋白病。通过活检获得的腓肠神经和皮神经标本显示髓鞘片上有IgM沉积。ELISA技术测定,两名患者的血清中均含有针对牛周围神经髓鞘的抗体,间接免疫荧光组织化学证明也含有针对正常人周围神经髓鞘的抗体。这些兄弟姐妹可能具有以周围神经髓鞘为免疫攻击靶点形成自身抗体的遗传易感性。