RSS-Feed abonnieren
DOI: 10.1055/s-0029-1243632
© Georg Thieme Verlag KG Stuttgart · New York
Spontaneous Resolution of Lymphatic and Venous Malformations
Publikationsverlauf
Publikationsdatum:
22. Januar 2010 (online)

Introduction
Vascular anomalies are broadly divided into two categories: vascular tumors and vascular malformations [8]. The former are characterized by growth during infancy and involution during childhood, while the latter, including venous (VM) and lymphatic malformations (LM), are considered developmental errors and are composed of dysmorphic vessels that “almost never regress” [8].This classification essentially dismisses the possibility of spontaneous resolution of these malformations, with surgical resection considered the only way to “cure” them [8].
Cervical LM, previously referred to as cystic hygroma, is a relatively rare lesion that is usually diagnosed in infancy or early childhood. Complete surgical extirpation, long considered the mainstay of treatment for these lesions, may be impossible without sacrificing important neurovascular structures, resulting in significant morbidity [1] [3] [4] [7] [17] [19] [21]. Postoperative recurrence rates are high [1] [3] [4] [7] [17] [19] [21]. Sclerotherapy with a variety of agents has also been reported in the literature as a primary treatment or as an adjunct to surgical excision [2] [5] [14] [15] [16] [18] [19] [20]. Each method of sclerotherapy is associated with potential complications and a significant chance of failure. Although spontaneous resolution or regression has been randomly documented in the literature [1] [4] [7], the option to observe an asymptomatic LM is not entertained by most pediatric surgeons.
Like LM, VM can also occur in any region of the body, including the head and neck [8] [6] [11] [20] [22]. The risk of hemorrhage is high with surgical resection. Sclerotherapy of VM has been described, but requires significant expertise that may not be available in many pediatric surgical centers [9] [10] [13]. To our knowledge, no reports exist of spontaneous resolution of VM.
In this report, we present two patients whose vascular malformations spontaneously resolved. The literature will also be reviewed to highlight the indications for observation of asymptomatic lesions.
References
- 1
Alqahtani A, Nguyen LT, Flageole H. et al .
25 years’ experience with lymphangiomas in children.
J Pediatr Surg.
1999;
34
1165-1168
MissingFormLabel
- 2
Castanon M, Margarit J, Carrasco R. et al .
Long-term follow-up of nineteen cystic lymphangiomas treated with fibrin sealant.
J Pediatr Surg.
1999;
34
1276-1279
MissingFormLabel
- 3
Charabi B, Bretlau P, Bille M. et al .
Cystic hygroma of the head and neck – a long-term follow-up of 44 cases.
Acta Otolaryngol.
2000;
543
248-250
MissingFormLabel
- 4
Dasgupta R, Adams D, Elluru R. et al .
Noninterventional treatment of selected head and neck lymphatic malformations.
J Pediatr Surg.
2008;
43
869-873
MissingFormLabel
- 5
Emran MA, Dubois J, Laberge L. et al .
Alcoholic solution of zein (Ethibloc) sclerotherapy for treatment of lymphangiomas
in children.
J Pediatr Surg.
2006;
41
975-979
MissingFormLabel
- 6
Fishman SJ, Shamberger RC, Fox VL. et al .
Endorectal pull-through abates gastrointestinal hemorrhage from colorectal venous
malformations.
J Pediatr Surg.
2000;
35
982-984
MissingFormLabel
- 7
Kennedy TL, Whitaker M, Pellitteri P. et al .
Cystic hygroma/lymphangioma: a rational approach to management.
Laryngoscope.
2001;
111
1929-1937
MissingFormLabel
- 8 Klement G, Fishman SJ. Vascular anomalies: hemangiomas and malformations. In: Grosfeld JL, et al., eds
Pediatric Surgery, 6th ed . Philadelphia, PA, Mosby 2006 pp. 2094-2110MissingFormLabel - 9
Lee BB, Bergan JJ.
Advanced management of congenital vascular malformations: a multidisciplinary approach.
J Cardiovasc Surg.
2002;
10
523-533
MissingFormLabel
- 10
Lee BB, Do YS, Byun HS. et al .
Advanced management of venous malformation (VM) with ethanol sclerotherapy: mid-term
results.
J Vasc Surg.
2003;
37
533-538
MissingFormLabel
- 11
Lee B-B, Choe YH, Ahn JM. et al .
The new role of magnetic resonance imaging in the contemporary diagnosis of venous
malformation: can it replace angiography?.
J Am Coll Surg.
2004;
198
549-558
MissingFormLabel
- 12
Nehra D, Jacobson L, Barnes P. et al .
Doxycycline sclerotherapy as primary treatment of head and neck lymphatic malformations
in children.
J Pediatr Surg.
2008;
43
451-460
MissingFormLabel
- 13
Nishikawa M, Sakamoto K, Hidaka M. et al .
Venous malformation of the tongue in a child treated by sclerotherapy with ethonalamine
oleate: a case report.
J Pediatr Surg.
2006;
41
599-600
MissingFormLabel
- 14
Ogita S, Tsuto T, Nakamura K. et al .
OK-432 therapy in 64 patients with lymphangioma.
J Pediatr Surg.
1994;
29
784-785
MissingFormLabel
- 15
Ogita S, Tsuto T, Nakamura K. et al .
OK-432 therapy for lymphangioma in children: why and how does it work?.
J Pediatr Surg.
1996;
31
477-480
MissingFormLabel
- 16
Okada A, Kubota A, Fukuzawa M. et al .
Injection of bleomycin as a primary therapy of cystic lymphangioma.
J Pediatr Surg.
1992;
27
440-443
MissingFormLabel
- 17
Okazaki T, Iwatani S, Yanai T. et al .
Treatment of lymphangioma in children: our experience of 128 cases.
J Pediatr Surg.
2007;
42
386-389
MissingFormLabel
- 18
Orford J, Barker A, Thonell S. et al .
Bleomycin therapy for cystic hygroma.
J Pediatr Surg.
1995;
30
1282-1287
MissingFormLabel
- 19
Ricciardelli EJ, Richardson MA.
Cervicofacial cystic hygroma.
Arch Otolaryngol Head Neck Surg.
1991;
117
546-553
MissingFormLabel
- 20
Samuel M, McCarthy L, Boddy SA.
Efficacy and safety of OK-432 sclerotherapy for giant cystic hygroma in a newborn.
Fetal Diagn Ther.
2000;
15
93-96
MissingFormLabel
- 21
Seashore JH, Gardiner LJ, Ariyan S.
Management of giant cystic hygromas in infants.
Am J Surg.
1985;
149
459-465
MissingFormLabel
- 22
Vogel AM, Alesbury JM, Burrows PE. et al .
Vascular anomalies of the female external genitalia.
J Pediatr Surg.
2006;
41
993-999
MissingFormLabel
Correspondence
Dr. Sherif Emil
Montreal Children's Hospital
Division of Pediatric General Surgery
2300 Tupper, Room C-818
Montreal, Quebec H3H 1P3
Canada
Telefon: 514 412 4497
Fax: 514 412 4289
eMail: sherif.emil@mcgill.ca