
TWO CASES OF NEVOID BASAL CELL CARCINOMA SYNDROME
Author(s) -
Satoh Masanobu,
Fukazawa Hajime,
Yagawa Kanichi,
Endo Hayato,
Suzuki Atsumi,
Yanagisawa Toru,
Kojima Makoto
Publication year - 1977
Publication title -
acta patholigica japonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
ISSN - 0001-6632
DOI - 10.1111/j.1440-1827.1977.tb00187.x
Subject(s) - frontal bossing , falx cerebri , nevoid basal cell carcinoma syndrome , pathology , medicine , anatomy , ossification , calcification , basal cell carcinoma , frontal bone , psammoma body , foramen ovale (heart) , hypertelorism , skull , surgery , basal cell , immunohistochemistry , percutaneous , patent foramen ovale
Two cases of nevoid basal cell carcinoma syndrome were reported with a review of pertinent literature. The first case was a 59‐year‐old man, whose autopsy was warranted. Signs and symptoms manifested in this case were basal cell carcinoma, generalized multiple nevi, multiple cysts in the jaws and long bones, pits in the palm and sole, frontal and occipital bossing, ossification of the falx cerebri, a bifid rib, renal fibroma and a patent foramen ovale. The family history revealed a hereditary predisposition as to the syndrome. The patient in the second case was a 25‐year‐old man who is still alive. Manifestations in this case included basal cell carcinoma, multiple nevi, multiple jaw cysts, pits in the palm and sole, frontal bossing, calcification of the falx cerebri, cervical vertebral fusion and high‐arched palate. ACTA PATH. JAP. 27: 713 ˜ 727, 1977.