“…Multiple subcutaneous and submucosal masses of either fibrous or non-fibrous origin, with or without visceral involvement, have been reported in many different conditions, such as neurofibromatosis (Riccardi, 1981), amyloidosis (Michaels and Hyams, 1979; Barnes and Zafar, 1977;Gottschalk and Graham, 1975), Gardner's syndrome (Weary et ai, 1964), multifocal fibrosclerosis (Comings et ai, 1967;Parington, 1961;Hamilton and Thiru, 1983;Coopersmith and Appelman, 1971), and familial multicentric fibromatosis (Zayid and Dihmis, 1969).…”