RESUMEN
Microvasculitis may play a greater part in the pathogenesis of paraproteinaemic neuropathies than is generally recognised, producing tissue destruction by convergent immune and physical mechanisms. We present a patient with a clinical syndrome of mononeuritis multiplex and a circulating IgM lambda paraprotein, in whom bone marrow aspiration revealed a lymphoplasmacytoid lymphoma. Microvasculitic changes were present in the first nerve biopsy, and the second showed extensive destruction of neural architecture and deposition of IgM-related material. A 2-stage pathogenic cascade is postulated and explored with a review of the relevant literature.
Asunto(s)
Linfoma de Células B/complicaciones , Paraproteinemias/complicaciones , Polineuropatías/complicaciones , Vasculitis/etiología , Anciano , Complejo CD3/metabolismo , Técnicas Electrofisiológicas Cardíacas/métodos , Endotelio/ultraestructura , Fascia , Humanos , Inmunoglobulina M/metabolismo , Linfoma de Células B/metabolismo , Masculino , Microcirculación/ultraestructura , Microscopía Electrónica , Mononeuropatías/etiología , Conducción Nerviosa , Paraproteinemias/metabolismo , Paraproteínas/metabolismo , Polineuropatías/metabolismo , Literatura de Revisión como AsuntoRESUMEN
Four loose ligatures were tied round the sciatic nerve of rats to produce the model of altered pain sensation first described by Bennett and Xie (1988). Hyperalgesia and hyperaesthesia were detected from 4 days after tying ligatures, becoming maximal after 14 days; normal behaviour returned by 8 weeks post-operation. Using thermal tests involving immersion of the whole foot, it was found that section of the saphenous nerve at the time of, or within a week of, placing ligatures had the effect of abolishing the hyperaesthetic behaviour and instead caused hypoaesthesia from the 4th to 10-12th days. There was then a change to hyperaesthetic behaviour. The findings are interpreted as indicating that the early hyperaesthesia is possibly due to collateral sprouting, spreading nociceptor sensitivity of saphenous nerve fibres or both of these.