A Very Rare Case of Hypertrophic Neuropathy with Left Ulnar Nerve Palsy
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Hypertrophic neuropathy is knoun as Charcot-Marie-Tooth type (HMSNI) or Dèjerine-Sottas disease. Both are hereditary, and there appear symmetrical lower limb symptoms in childhood. This case, a 60 years old male, however, had asymmetrical upper limb symptoms with ulnar nerve palsy, and had no family history. His cheif complaints were feeling of numbness, muscular weakness and muscular atrophy on his left hand.The first diagnosis was delayed palsy of left ulnar nerve, but no therapy was effective. Later he complained of pain in his left axillar legion. There was a tumor palpable.Then biopsy was made, and the histological diagnosis was hypertrophic neuropathy.This is a very rare case. We found no paper reported like this case. This case has to be called mortor and sensory type of hypertrophic neuropathy
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