Surgical management of vascular anomalies in children at a tertiary care hospital in a resource-limited setting: a Tanzanian experience with 134 patients
Open Access
- 30 November 2015
- journal article
- research article
- Published by Springer Nature in BMC Research Notes
- Vol. 8 (1) , 732
Abstract
Background: Vascular anomalies pose major diagnostic and therapeutic challenges among pediatricians and pediatric surgeons practicing in resource limited countries. There is paucity of published data regarding this subject in Tanzania and Bugando Medical Centre in particular. This study describes our experiences on the challenges and outcome of surgical management of childhood vascular anomalies in our environment.Methods: Between January 2009 and December 2013, a prospective study on the surgical management of vascular anomalies was undertaken at Bugando Medical Centre.Results: A total of 134 patients (M; F = 1:2.5) were studied. The median age at presentation was 6 years. Of the 134 patients, 101 (75.4 %) were diagnosed as having vascular tumors and 33 (24.6 %) had vascular malformations. The head and the neck were the most frequent anatomical site recorded as having a tumor (56.7 % of patients). Out of 134 patients, 129 (96.3 %) underwent surgical treatment. Failure to respond to non-operative treatment (86.8 %), huge disfiguring/obstructing mass (4.7 %), infection (3.1 %), ulceration (3.1 %) and hemorrhage (2.3 %) were indications for surgical intervention. Tumor excision and primary wound closure was the most common type of surgical procedure performed in 80.6 % of patients. Surgical site infection was the most frequent complications accounting for 33.8 % of cases. Mortality rate was 1.5 %. Tumor excision and primary wound closure gave better outcome compared with other surgical options (p < 0.001). Outcome of injection sclerotherapy in 3 (3.7 %) children, serial ligation of feeder vessels employed in 2 (1.6 %), and conservative treatment in 5 (3.7 %), were poor and required conversion to surgical excision. Despite low mortality rate recorded in this study, but ugly scar, 14 (20.6 %) and limb deformity, 6 (8.8 %) were problems. The overall result of surgical treatment at the end of follow up period was excellent in 108 (87.1 %) patients.Conclusion: Surgical excision and primary wound closure gave good outcome which could be employed in complicated and vascular anomalies which failed to respond to other treatment in regions with limited resources.Keywords
This publication has 34 references indexed in Scilit:
- Infantile hemangioma: An updateIndian Journal of Dermatology, Venereology and Leprology, 2010
- Segmental Hemangioma of Infancy Complicated by Life‐Threatening Arterial BleedPediatric Dermatology, 2009
- Reticular Infantile Hemangioma of the Limb Can Be Associated with Ventral‐Caudal Anomalies, Refractory Ulceration, and Cardiac OverloadPediatric Dermatology, 2007
- Prospective Study of Infantile Hemangiomas: Clinical Characteristics Predicting Complications and TreatmentPediatrics, 2006
- Congenital hemangiomas and infantile hemangioma: missing linksJournal of the American Academy of Dermatology, 2004
- Molecular Pathogenesis of Vascular Anomalies: Classification into Three Categories Based upon Clinical and Biochemical CharacteristicsLymphatic Research and Biology, 2003
- Hemoperitoneum from a Spontaneous Rupture of a Giant Hemangioma of the Liver: Report of a CaseSurgery Today, 2003
- Congenital hemangioma: Evidence of accelerated involutionThe Journal of Pediatrics, 1996
- Congenital vascular lesions: Clinical application of a new classificationJournal of Pediatric Surgery, 1983
- Hemangiomas and Vascular Malformations in Infants and ChildrenPlastic and Reconstructive Surgery, 1982