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Original Article

Ethanol Sclerotherapy Reduces Pain in Symptomatic Musculoskeletal Hemangiomas

Eileen A. Crawford1, Rachel L. Slotcavage1, Joseph J. King2, Richard D. Lackman1 and Christian M. OgilvieContact Information

(1)  Department of Orthopaedic Surgery, University of Pennsylvania, Garfield Duncan Building, Suite 2C, 301 South 8th Street, Philadelphia, PA 19106-6192, USA
(2)  Department of Orthopaedic Surgery, Drexel University, Philadelphia, PA, USA

Received: 7 October 2008  Accepted: 21 May 2009  Published online: 18 June 2009

Abstract  Hemangiomas, benign vascular lesions, require intervention if causing pain or functional limitations. Functional deficits are common after excision, favoring minimally invasive treatments. To determine whether ethanol sclerotherapy reduces pain and lesion size and to assess complications in symptomatic musculoskeletal hemangiomas, we retrospectively reviewed 19 patients (six males, 13 females; mean age, 34 years) meeting criteria of confirmed hemangioma, treatment with ethanol sclerotherapy, and minimum of 6 weeks of followup. Fourteen were primary lesions and five were recurrent; all were painful. Thirty-eight sclerotherapy procedures were performed, with each patient undergoing a maximum of three procedures. Mean followup was 24 months (range, 2–95 months). Four patients reported full pain relief, 11 had partial relief, and four had no relief. With recurrent lesions, one patient had full pain relief, one had partial relief, and three had no relief. For patients with lesions larger than 5 cm, two had full relief, six had partial relief, and three had no relief. Lesion shrinkage occurred in 12 patients. Temporary complications included paresthesiae (three), tendon contracture (one), skin breakdown (one), and deep vein thrombosis (one). Ethanol sclerotherapy afforded prompt pain relief in 15 of 19 patients with hemangioma, making it a reasonable option for initially avoiding surgical excision. However, the short followup of our patients requires additional long-term studies to assess the duration of the results.
Level of Evidence: Level IV, therapeutic study. See Guidelines for Authors for a complete description of levels of evidence.
One or more of the authors (EAC, RLS, JJK) received funding in the form of a research fellowship from Stryker Orthopaedics, Mahwah, NJ. One of the authors (RDL) is a consultant for Stryker Orthopaedics, Mahwah, NJ.
Each author certifies that his or her institution has approved or waived approval for the human protocol for this investigation and that all investigations were conducted in conformity with ethical principles of research.
This work was performed at University of Pennsylvania.

Contact Information Christian M. Ogilvie
Email: christian.ogilvie@uphs.upenn.edu
Email: christianogilvie@yahoo.com

References

1. Bella GP, Manivel JC, Thompson RC Jr, Clohisy DR, Cheng EY. Intramuscular hemangioma: recurrence risk related to surgical margins. Clin Orthop Relat Res. 2007;459:186–191.
PubMed CrossRef
 
2. Burrows PE, Mason KP. Percutaneous treatment of low flow vascular malformations. J Vasc Interv Radiol. 2004;15:431–445.
PubMed
 
3. Canavese F, Soo BC, Chia SK, Krajbich JI. Surgical outcome in patients treated for hemangioma during infancy, childhood, and adolescence: a retrospective review of 44 consecutive patients. J Pediatr Orthop. 2008;28:381–386.
PubMed
 
4. Enzinger F, Weiss S. Benign Tumors and Tumorlike Lesions of Blood Vessels in Soft Tissue Tumors. St. Louis, MO: CV Mosby; 1995.
 
5. Goyal M, Causer PA, Armstrong D. Venous vascular malformations in pediatric patients: comparison of results of alcohol sclerotherapy with proposed MR imaging classification. Radiology. 2002;223:639–644.
PubMed CrossRef
 
6. Hayashi N, Masumoto T, Okubo T, Abe O, Kaji N, Tokioka K, Aoki S, Ohtomo K. Hemangiomas in the face and extremities: MR-guided sclerotherapy—optimization with monitoring of signal intensity changes in vivo. Radiology. 2003;226:567–572.
PubMed CrossRef
 
7. Hein KD, Mulliken JB, Kozakewich HP, Upton J, Burrows PE. Venous malformations of skeletal muscle. Plast Reconstr Surg.2002;110:1625–1635.
PubMed CrossRef
 
8. Matsumoto K, Nakanishi H, Koizumi Y, Seike T, Kanda I, Kubo Y. Sclerotherapy of hemangioma with late involution. Dermatol Surg. 2003;29:668–671; discussion 671.
PubMed CrossRef
 
9. O’Donovan JC, Donaldson JS, Morello FP, Pensler JM, Vogelzang RL, Bauer B. Symptomatic hemangiomas and venous malformations in infants, children, and young adults: treatment with percutaneous injection of sodium tetradecyl sulfate. AJR Am J Roentgenol. 1997;169:723–729.
PubMed
 
10. Puig S, Aref H, Brunelle F. Double-needle sclerotherapy of lymphangiomas and venous angiomas in children: a simple technique to prevent complications. AJR Am J Roentgenol. 2003;180:1399–1401.
PubMed
 
11. Tang P, Hornicek FJ, Gebhardt MC, Cates J, Mankin HJ. Surgical treatment of hemangiomas of soft tissue. Clin Orthop Relat Res. 2002;399:205–210.
PubMed CrossRef
 
12. Upton J, Coombs C, Mulliken J, Burrows P, Pap S. Vascular malformations of the upper limb: a review of 270 patients. J Hand Surg Am. 1999;24:1019–1035.
PubMed CrossRef ChemPort
 
13. Wild AT, Rabb P, Krauspe R. Hemangioma of skeletal muscle. Arch Orthop Trauma Surg. 2000;120:139–143.
PubMed SpringerLink ChemPort
 
14. Winter H, Drager E, Sterry W. Sclerotherapy for treatment of hemangiomas. Dermatol Surg. 2000;26:105–108.
PubMed CrossRef ChemPort
 
15. Wisniewski SJ, Newcomer K, Stanson AW. Intramuscular hemangioma of the foot: a diagnostic dilemma. Med Sci Sports Exerc. 2005;37:1655–1657.
PubMed CrossRef
 
16. Yakes WF, Haas DK, Parker SH, Gibson MD, Hopper KD, Mulligan JS, Pevsner PH, Johns JC Jr, Carter TE. Symptomatic vascular malformations: ethanol embolotherapy. Radiology. 1989;170:1059–1066.
PubMed ChemPort
 
17. Yakes WF, Luethke JM, Parker SH, Stavros AT, Rak KM, Hopper KD, Dreisbach JN, Griffin DJ, Seibert CE, Carter TE, et al. Ethanol embolization of vascular malformations. Radiographics. 1990;10:787–796.
PubMed ChemPort
 


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