Premium
Heterogeneity in the gingival fibromatoses
Author(s) -
Takagi Minoru,
Yamamoto Hajime,
Mega Hiroko,
Hsieh Kuo Jeng,
Shioda Shigetoshi,
Enomoto Shoji
Publication year - 1991
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19911115)68:10<2202::aid-cncr2820681019>3.0.co;2-o
Subject(s) - medicine , fibromatosis , hypertrichosis , gingival enlargement , genetic heterogeneity , gingivectomy , dermatology , pedigree chart , pathology , dentistry , genetics , phenotype , gene , biology
Forty‐nine cases of isolated familial and idiopathic gingival fibromatoses, consisting of 12 cases from six families and 37 cases of idiopathic gingival fibromatosis, were reviewed. Pedigrees of five families revealed various penetrances and genetic heterogeneity as suggested by the presence of both autosomal dominant and autosomal recessive inheritances. Ultrastructurally, the lesions were composed of fibroblast‐like cells and myofibroblast‐like cells, with the former being the predominant cell type. The 267 cases of familial and idiopathic gingival fibromatoses were analyzed, and they with or without hypertrichosis, mental retardation, and/or epilepsy. These included 49 cases seen by the authors, 50 cases from the Japanese literature, and 168 cases from non‐Japanese literature. Isolated gingival fibromatosis occurred more frequently after age of 12 years ( P < 0.007). There was no significant difference in age of onset between generalized and localized forms of the idiopathic gingival fibromatosis. Gingival fibromatosis with hypertrichosis and mental retardation and/or epilepsy occurred frequently before 12 years ( P < 0.069). It has been shown that heterogeneity of the gingival fibromatosis is a result of either histologic heterogeneity, genetic heterogeneity, or a combination with other systemic disorders. Cancer 68:2202–2212, 1991.