Vital C, Gherardi R, Vital A, Kopp N, Pellissier J F, Soubrier M, Clavelou P, Bellance R, Delisle M B, Ruchoux M M
Laboratoire d'Anatomie-Pathologique, Hôpital Pellegrin, Bordeaux, France.
Acta Neuropathol. 1994;87(3):302-7. doi: 10.1007/BF00296746.
Mechanisms of peripheral neuropathies in polyneuropathy, organomegaly, endocrinopathy, M-protein and skin changes (POEMS) syndrome are poorly understood. A peripheral nerve biopsy was performed in 22 patients. Of these 9 had histological features of Castleman's disease on lymph node biopsies, and 19 had a monoclonal lambda light chain in their serum. Certain nerve fragments were paraffin embedded, others were frozen and studied by direct immunofluorescence, and others were fixed for ultrastructural examination. Paraffin-embedded fragments did not show any amyloid deposits, and at direct immunofluorescence there was no immunoglobulin fixation. At ultrastructural examination, features of uncompacted myelin lamellae (UML) were present in 19 patients, and their frequency varied from 1% to 16% of myelinated fibres. Up to now UML have been reported only in 7 patients with POEMS syndrome in the literature. UML have also been noticed in a few cases of inflammatory demyelinating polyradiculoneuritis and inherited tendency to pressure palsy.
多神经病、器官肿大、内分泌病、M蛋白血症和皮肤改变(POEMS)综合征中周围神经病变的机制尚不清楚。对22例患者进行了周围神经活检。其中9例在淋巴结活检中有Castleman病的组织学特征,19例血清中有单克隆λ轻链。部分神经碎片用石蜡包埋,其他的冷冻后进行直接免疫荧光研究,还有一些固定后进行超微结构检查。石蜡包埋的碎片未显示任何淀粉样沉积物,直接免疫荧光检查未发现免疫球蛋白固定。超微结构检查发现,19例患者存在疏松髓鞘板层(UML)特征,其在有髓纤维中的发生率从1%到16%不等。迄今为止,文献中仅报道了7例POEMS综合征患者有UML。在少数炎症性脱髓鞘性多发性神经根神经炎和遗传性压迫性麻痹病例中也发现了UML。