T. Zander et al., Immunohistochemical detection of complement factors: a reliable method forthe diagnosis of myasthenia gravis, NERVENARZT, 71(8), 2000, pp. 666-669
A 57-year-old woman suffered from generalized muscular weakness without dip
lopia or dysphagia for about 2 years. An abnormal decremental response on l
ow frequency nerve stimulation and improvement upon administration of edrop
honium chloride suggested a diagnosis of myasthenia gravis. However,this di
agnosis remained uncertain, since repeated tests for antiacetylcholine rece
ptor antibodies were negative. In addition, the patient reported that she w
as never able to keep up with peers in prolonged physical activities since
childhood. For this reason, a congenital myasthenic syndrome was suspected
and an intercostal muscle biopsy performed for special end-plate studies. I
mmunohistochemistry of the muscle biopsy revealed membrane attack complex d
eposits at the end-plates. This finding definitely confirmed the diagnosis
of autoimmune myasthenia gravis. In conclusion, immunohistochemistry for co
mplement deposits at the end-plates is a simple and reliable method of conf
irming the diagnosis of myasthenia gravis in uncertain cases.