Vital Anne, Nedelec-Ciceri Claudine, Vital Claude
CNRS UMR 5227, Victor Segalen-Bordeaux 2 University, France.
Neuropathology. 2008 Oct;28(5):526-31. doi: 10.1111/j.1440-1789.2008.00875.x. Epub 2008 Apr 11.
Association of a peripheral neuropathy with an IgA monoclonal gammopathy of undetermined significance (MGUS) is not commonly observed and is sometimes considered as coincidental. We present a case in which the nerve biopsy revealed the presence of crystalline inclusions in the endoneurium, a very unusual finding. A 75-year-old man complained of paresthesiae in both feet and unsteady gait for 6 months. He had no weakness, but deep tendon reflexes were absent and vibratory sensation distally diminished in both legs. An IgA lambda MGUS was evidenced in his serum at 10.2 g/L with 7% plasma cells in his bone marrow and no lytic lesion at skeletal examination. A superficial peroneal nerve biopsy was performed and showed numerous crystalline inclusions in the endoneurium. These were located in the cytoplasm of macrophagic histiocytes or free in the vicinity of nerve fibers. There was also a marked loss of myelinated nerve fibers and several "onion bulb" formations surrounding either isolated remyelinating fibers or small clusters of remyelinating fibers. Such crystalline inclusions have mainly been observed in the cytoplasm of plasma cells in cases of multiple myeloma, and correspond to non-secreted IgA or IgG immunoglobulins with a kappa or rarely lambda light chain. Such inclusions have also been reported in the cytoplasm of the epithelial cells from corneal fragments, in patients with multiple myeloma or IgG MGUS, and in the tubular cells from the kidney of patients with multiple myeloma and a nephrotic syndrome. In the literature, there is only one very briefly mentioned case of neuropathy associated with a myeloma and with crystalline inclusions present in the epineurium. Thus, in dysglobulinemic neuropathy, nerve fibers can be damaged by three kinds of interstitial deposits, easily identified by immunohistochemistry and at ultrastructural examination: the well known amyloid fibrils, granulo-fibrillar deposits and also crystalline inclusions.
周围神经病变与意义未明的IgA单克隆丙种球蛋白病(MGUS)相关的情况并不常见,有时被认为是巧合。我们报告一例神经活检显示神经内膜存在结晶包涵体的病例,这是一个非常罕见的发现。一名75岁男性抱怨双足感觉异常和步态不稳6个月。他没有肌无力,但双侧深腱反射消失,双下肢远端振动觉减退。血清中IgA λ型MGUS的水平为10.2 g/L,骨髓中有7%的浆细胞,骨骼检查未发现溶骨性病变。进行了腓浅神经活检,显示神经内膜有大量结晶包涵体。这些包涵体位于巨噬细胞组织细胞的细胞质中或神经纤维附近。还存在明显的有髓神经纤维丢失,以及围绕孤立的再髓鞘化纤维或小簇再髓鞘化纤维的几个“洋葱球”形成。这种结晶包涵体主要在多发性骨髓瘤病例的浆细胞细胞质中观察到,对应于具有κ或很少λ轻链的非分泌型IgA或IgG免疫球蛋白。在多发性骨髓瘤或IgG MGUS患者的角膜碎片上皮细胞细胞质中,以及多发性骨髓瘤和肾病综合征患者的肾小管细胞中也报告有这种包涵体。在文献中,仅有一例与骨髓瘤相关且在神经外膜存在结晶包涵体的神经病变病例被非常简要地提及。因此,在球蛋白异常血症性神经病变中,神经纤维可被三种间质沉积物损伤,通过免疫组织化学和超微结构检查很容易识别:众所周知的淀粉样纤维、颗粒纤维状沉积物以及结晶包涵体。