Desmons F, Bombart M
Ann Dermatol Venereol. 1977 May;104(5):355-60.
Six personal cases of nodular congenital fibromatosis are reported: one fibromatosis colli, two fibromas of the fingers one multiple fibromas of the toes and sole associated with osteoporosis and underlying bone lacunes, one recurrent plantar fibromatosis, one disseminated fibromatosis with multiple bone lesions. Such varieties of fibromatosis are very uncommon. Few are isolated such as fibromatosis colli or the fibroma of the fingers. The prognosis is generally good except for the generalized multinodular form which associates a very large visceral involvement. Aetiology is completely unknown. Only few arguments are in favour of an hereditary dominant autosomal transmission of the diffuse multinodular form.
报告了6例结节性先天性纤维瘤病的个人病例：1例颈部纤维瘤病，2例手指纤维瘤，1例伴有骨质疏松和潜在骨腔隙的脚趾及足底多发纤维瘤，1例复发性足底纤维瘤病，1例伴有多发骨病变的播散性纤维瘤病。这种纤维瘤病的类型非常罕见。很少有孤立的病例，如颈部纤维瘤病或手指纤维瘤。除了伴有广泛内脏受累的全身性多结节形式外，预后通常良好。病因完全不明。仅有少数证据支持弥漫性多结节形式的常染色体显性遗传。
