Infantile myofibromatosis

Infantile myofibromatosis

Infantile myofibromatosis (also known as "Congenital generalized fibromatosis,"[1] and "Congenital multicentric fibromatosis"[1]) is the most common fibrous tumor of infancy, in which eighty percent of patients have solitary lesions with half of these occurring on the head and neck, and 60% are present at or soon after birth.[2]:606

See also

References

  1. ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0. 
  2. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.


Lipomatous (8850–8889)
Chondroid lipoma · Intradermal spindle cell lipoma · Pleomorphic lipoma · Benign lipoblastomatosis · Spindle cell lipoma · Hibernoma
Myomatous (8890–8929)
general: Myoma/myosarcoma
skeletal muscle: Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma (Sarcoma botryoides) · Alveolar rhabdomyosarcoma
Leiomyoma · Angioleiomyoma · Angiolipoleiomyoma · Genital leiomyoma · Leiomyosarcoma · Multiple cutaneous and uterine leiomyomatosis syndrome · Multiple cutaneous leiomyoma · Neural fibrolipoma · Solitary cutaneous leiomyoma
Complex mixed and stromal (8930–8999) Mesothelial (9050–9059)

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  • congenital generalized fibromatosis — a type of infantile myofibromatosis characterized by multiple small, firm, spherical or ovoid fibromas of subcutaneous tissue, muscle, viscera, and bone. Visceral involvement may be responsible for symptoms such as intestinal obstruction,… …   Medical dictionary

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