Literature DB >> 3331192

Desmoid tumors in childhood.

P Scougall1, L T Staheli, D E Chew, T K Taylor, E E Almquist.   

Abstract

Eight cases of extraabdominal desmoid tumors in children are reviewed. Seven were located in the pelvis or forearm, and the most common presenting complaint was a slowly enlarging mass. In all cases, diagnosis was established by open biopsy, and initial treatment was by surgical excision. At follow-up (average, 5.8 years), six patients were tumor free. Desmoids are benign tumors that usually carry a good prognosis. There is no difference between the tumor behavior in children and adults. The treatment of choice is wide local excision. If vital structures are involved, it may be more appropriate to preserve function by performing partial tumor excision. For quiescent recurrent tumors, observation is appropriate management, but if further treatment is required, reexcision or radiotherapy may be tried.

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Year:  1987        PMID: 3331192

Source DB:  PubMed          Journal:  Orthop Rev        ISSN: 0094-6591


  4 in total

1.  Development and rapid growth of a desmoid tumor in the surgical corridor after suboccipital craniotomy for recurrent low-grade astrocytoma.

Authors:  Todd McCall; Ganesh Rao; Randy Jensen
Journal:  J Neurooncol       Date:  2006-04-28       Impact factor: 4.130

Review 2.  Aggressive fibromatosis of the head and neck: a new classification based on a literature review over 40 years (1968-2008).

Authors:  Astrid L Kruse; Heinz T Luebbers; Klaus W Grätz; Joachim A Obwegeser
Journal:  Oral Maxillofac Surg       Date:  2010-12

3.  Infantile Fibromatosis: A Rare Cause of Anterior Mediastinal Mass in a Child.

Authors:  Venkatraman Bhat; Praveen Raju; Sanjay Rao; Srinivas Ramaiah
Journal:  J Clin Imaging Sci       Date:  2015-06-29

4.  Abdominal fibromatosis in a young child: a case study and review of the literature.

Authors:  Hyun Hee Chu; Pyoung Han Hwang; Yeon Jun Jeong; Myoung Ja Chung
Journal:  Korean J Pathol       Date:  2013-10-25
  4 in total

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