Strategies in Trauma and Limb Reconstruction

Register      Login

VOLUME 9 , ISSUE 2 ( August, 2014 ) > List of Articles

CASE REPORT

Complex reconstruction after wide excision of juvenile aponeurotic fibromatoses of upper one-third of leg

Md Sohaib Akhtar, Rabeya Basari, A. H. Khan, Mohd Fahud Khurram

Keywords : Juvenile musculoaponeurotic fibromatosis, Locally aggressive tumor, Complex reconstruction

Citation Information : Akhtar MS, Basari R, Khan AH, Khurram MF. Complex reconstruction after wide excision of juvenile aponeurotic fibromatoses of upper one-third of leg. 2014; 9 (2):117-120.

DOI: 10.1007/s11751-014-0195-x

License: CC BY-NC-SA 4.0

Published Online: 01-06-2018

Copyright Statement:  Copyright © 2014; The Author(s).


Abstract

Juvenile musculoaponeurotic fibromatoses are benign tumors which arise from musculoaponeurotic stromal cells. They rarely occur in lower extremity and more rarely in children. They are locally invasive tumors with a high incidence of recurrence after surgery. Hence, wide local excision is the treatment of choice for such tumors. However, complex reconstruction is often required to cover the resulting soft tissue defect. This report presents a 12-year-old boy with a juvenile musculoaponeurotic fibromatosis in the anteromedial aspect of the upper third of a left leg. Following wide local excision, two local flaps, medial gastrocnemius and a distally based peroneal artery perforator flap, were used to reconstruct the soft tissue defect. Reconstruction has provided an acceptable functional and cosmetic result.


PDF Share
  1. Stout AP (1954) Juvenile fibromatoses. Cancer 7:953-978
  2. Mackenzie DH (1972) The fibromatoses: a clinicopathological concept. Br Med J 4:277-281
  3. Tolhurst DE, Haeseker B, Zeeman RJ (1983) The development of fasciocutaneus flap and its application. Plast Reconstr Surg 71:597
  4. Mathes S, Nahai F (1982) Clinical application of muscles and musculocutaneous flaps. Mosby, St. Louis
  5. Chaudhuri B, Das Gupta TK (1998) Pathology of soft tissue sarcomas. In: Das Gupta TK, Chaudhuri PK (eds) Tumors of the soft tissues. Appleton and Lange, Stanford, pp 63-200
  6. Reitamo JJ, Scheinin TM, Havry P (1986) The desmoid syndrome. New aspects in the cause, pathogenesis and treatment of the desmoid tumor. Am J Surg 151:230-237
  7. Dahn J, Johnson N, Lundh G (1963) Desmoid tumours. A series of 33 cases. Acta Chir Scand 126:305-314
  8. McAdam WAF, Goligher JC (1970) The occurrence of desmoids in patients with familial polyposis coli. Br J Surg 57:618-631
  9. Hansmann A, Adolph C, Vogel T, Unger A, Moeslein G (2004) High-dose tamoxifen and sulindac as first-line treatment for desmoids tumors. Cancer 100:612-620
  10. Lee J, Glazer H (1990) Controversy in the MR imaging of fibrosis. Radiology 177:21-22
  11. Abbas AE, Deschamps C, Cassivi SD, Nichols FC III, Allen MS, Schleck CD, Pairolero PC (2004) Chest-wall desmoid tumors: results of surgical intervention. Ann Thorac Surg 78:1219-1223
  12. Lewis JJ, Boland PJ, Leung DH et al (1999) The enigma of desmoids tumors. Ann Surg 229:866-887
  13. Nuyttens JJ, Rust PF, Thomas CR, Turrisi AT III (2000) Surgery versus radiation therapy for patients with aggressive fibromatosis or desmoids tumors. A comparative review of 22 articles. Cancer 88:1517-1523
PDF Share
PDF Share

© Jaypee Brothers Medical Publishers (P) LTD.