（56）ブルヌビーユ・プリングル氏母斑症の1例

A case of Phakomatosis Bourneville-Pringli

I．緒言

　1880年Bourneville氏によつて始めて発見された本疾患は，現在Phakomttosis Burneville-Pringliと呼ばれ，稀有な疾患の一つに数えられて居る。本疾患は癲癇発作，精神発育障碍，脂腺腫，網膜母斑症を主徴候とし，其の他に脊椎破裂，頭蓋畸型，馬蹄腎，等々の先天性畸型を合併する。私は今回本症の不全型と思われる症例に接したので眼科的所見をのべて，諸賢の参考に供したいと思う。

The following is the views which I got from a case of phatsomatosis Bourneville-Pringli.

The case is a boy of eight years and seven months old whose family anamnesis seems to have no special hereditary relation with phakomatosis Bourneville-Pringli. His constitution and condition of nutrition was average and I could not find any remarkable internal change in him. Two years ago a tumor of fat gland was produced on his face and the number of the tumor gradually increased. No disturbance of mental development, no epileptic fit and no congenital deformity.