The Crow‐Fukase syndrome

Takao Nakanishi(National Center of Neurology and Psychiatry), I Sobue(National Center of Neurology and Psychiatry), Y Toyokura(National Center of Neurology and Psychiatry), Hiroshi Nishitani(National Center of Neurology and Psychiatry), Yoshigoro Kuroiwa(National Center of Neurology and Psychiatry), E Satoyoshi(National Center of Neurology and Psychiatry), T Tsubaki(National Center of Neurology and Psychiatry), A Igata(National Center of Neurology and Psychiatry), Yukio Ozaki(National Center of Neurology and Psychiatry)
Neurology
June 1, 1984
Cited by 558

Abstract

Clinical manifestations of 102 cases with the Crow- Fukase syndrome (the syndrome of polyneuropathy, anasarca, skin changes, endocrinopathy, dysglobulinemia, and organomegaly), with or without myeloma, were reviewed. Fifty-six cases with myeloma consisted of 31 with osteosclerotic, 17 with mixed osteosclerotic and osteolytic, and 8 with osteolytic. Forty-six cases without myeloma consisted of 2 with extramedullary plasmacytoma, 33 with M protein alone, and 11 with polyclonal protein alone. There was no significant difference in incidence of the major clinical manifestations between the two groups with and without myeloma. They had a common characteristic histologic finding of the lymph node resembling that of Castleman's disease.


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