Fibromatosis Explained

Fibromatosis
Field:oncology

The term fibromatosis refers to a group of soft tissue tumors which have certain characteristics in common, including absence of cytologic and clinical malignant features, a histology consistent with proliferation of well-differentiated fibroblasts, an infiltrative growth pattern, and aggressive clinical behavior with frequent local recurrence. It is classed by the World Health Organization as an intermediate soft tissue tumor related to the sarcoma family. Arthur Purdy Stout coined the term fibromatosis (in the name congenital generalized fibromatosis, describing myofibromatosis), in 1954.[1]

Diagnosis

Juvenile subtypes

Subtypes of juvenile fibromatosis include:[2]

Adult subtypes

Superficial

Deep

Treatment

Treatment is mainly surgical; radiotherapy or chemotherapy is usually an indication of relapse. Head and neck desmoid fibromatosis is a serious condition due to local aggression, specific anatomical patterns and the high rate of relapse. For children surgery is particularly difficult, given the potential for growth disorders.[5]

Treatment includes prompt radical excision with a wide margin and/or radiation. For aggressive fibromatosis, the consensus on treatment is observation for new tumors rather than immediate surgery.[6] Despite their local infiltrative and aggressive behavior, mortality is minimal to nonexistent for peripheral tumors. In intra-abdominal fibromatosis associated with familial adenomatous polyposis (FAP), surgery is avoided if possible due to high rates of recurrence within the abdomen carrying significant morbidity and mortality. Conversely, for intra-abdominal fibromatosis without evidence of FAP extensive surgery may still be required for local symptoms, but the risk of recurrence is low.[7]

Terminology

Other names include musculoaponeurotic fibromatosis, referring to the tendency of these tumors to be adjacent to and infiltrating deep skeletal muscle, aggressive fibromatosis and desmoid tumor. A clear difference should be made between intra-abdominal and extra-abdominal localizations. Fibromatosis is a different entity from neurofibromatosis.

Notes and References

  1. Beck . Jill C. . Devaney . Kenneth O. . Weatherly . Robert A. . Koopmann . Charles F. . Lesperance . Marci M. . 1999-01-01 . Pediatric Myofibromatosis of the Head and Neck . . 125 . 1 . 39 . 10.1001/archotol.125.1.39 . 9932585 . 0886-4470. free .
  2. Web site: Fibromatosis . 2023-08-15 . DermNet.
  3. Lavie JL, Rogers CL, Stalder MW, St Hilaire H . January 2021 . Primary Resection and Immediate Autologous Reconstruction of Fronto-orbital Infantile Myofibromatoses . Plastic and Reconstructive Surgery. Global Open . 9 . 1 . e3261 . 10.1097/GOX.0000000000003261 . 7858576 . 33552804.
  4. Durnford L, Patel MS, Khamar R, Khurram R . Bilateral sternocleidomastoid pseudotumors-a case report and literature review . Radiology Case Reports . 16 . 4 . 964–967 . April 2021 . 33664922 . 7897923 . 10.1016/j.radcr.2021.02.001 .
  5. Cecilia Petrovan, Diana Nekula. Submandibular juvenile desmoid fibromatosis: case report of a 2 years old child. ro. Rev. chir. oro-maxilo-fac. implantol.. 2069-3850. 2. 3. 15–19. Nov 2011. 41. 2012-06-06. (webpage has a translation button)
  6. Kasper . B. . Baumgarten . C. . Garcia . J. . Bonvalot . S. . Haas . R. . Haller . F. . Hohenberger . P. . Penel . N. . Messiou . C. . van der Graaf . W.T. . Gronchi . A. . Bauer . S. . Blay . J.Y. . van Coevorden . F. . Dileo . P. . October 2017 . An update on the management of sporadic desmoid-type fibromatosis: a European Consensus Initiative between Sarcoma PAtients EuroNet (SPAEN) and European Organization for Research and Treatment of Cancer (EORTC)/Soft Tissue and Bone Sarcoma Group (STBSG) . . 28 . 10 . 2399–2408 . 10.1093/annonc/mdx323 . 5834048 . 28961825.
  7. Wilkinson MJ, Fitzgerald JE, Thomas JM, Hayes AJ, Strauss DC. 205512855. 2012. Surgical resection for non familial adenomatous polyposis related intra-abdominal fibromatosis. British Journal of Surgery. Semantic Scholar. 99. 5. 706–713. 10.1002/bjs.8703. 22359346.