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1.
Carcinologie Pratique en Afrique ; 16(1): 9-12, 2018. ilus
Article in French | AIM | ID: biblio-1260272

ABSTRACT

Le néphroblastome est le deuxième cancer de l'enfant à Brazzaville. Nous avons mené cette étude afin d'en dégager les principales caractéristiques et les difficultés de leur prise en charge à Brazzaville au Congo.Il s'était agi d'une étude descriptive transversale sur une période de six ans (2008-2013). Nous avions ainsi colligé les patients atteints de néphroblastome dont nous avons décrits les aspects épidémiologiques, cliniques et thérapeutiques. Durant la période d'étude, 52 enfants, âgés de 0 à 14 ans avaient été colligés, dont 14 pour néphroblastome. Nous avions constaté une prédominance féminine et l'âge moyen au diagnostic était de 50,6 mois. La masse abdominale était la principale circonstance de découverte. Un cas de néphroblastome bilatéral avait été retrouvé. La survie globale à 6 mois, était de d'environ 65 %


Subject(s)
Academic Medical Centers , Congo , Disease Management , Genes, Wilms Tumor , Wilms Tumor/diagnosis , Wilms Tumor/epidemiology , Wilms Tumor/therapy
2.
S. Afr. j. child health (Online) ; 8(4): 128-132, 2014.
Article in English | AIM | ID: biblio-1270439

ABSTRACT

Background. Nephroblastoma is one of the most common childhood malignancies in Africa; but with a survival rate significantly lower than in developed countries. In African countries with a small gross domestic product (GDP) per capita; the cost of treating nephroblastoma may be prohibitive. Objectives. To determine the direct costs of treatment of nephroblastoma in South Africa (SA) and to propose a more cost-effective approach to investigations and treatment for the disease in Africa. Methods. Data from 2000 - 2010 from two SA paediatric oncology units were retrospectively analysed. The costs included investigations; chemotherapy and radiotherapy; comparing early-v. advanced-stage disease. In both units; the nephroblastoma International Society of Paediatric Oncology (SIOP) protocol was used. Results. Stage I disease was the most common; followed by stage IV. The total cost of diagnosis; staging and treatment of stage I disease was ZAR9 304.97 (EUR882.80 or USD1 093.40); compared with a five-times higher cost for stage IV (ZAR48 293.62 (EUR4 581.9 or USD5 674.9)). Treating one patient averted more than 32 disability adjusted life years. The investigation and treatment of early- and advanced-stage disease is very cost-effective when compared with the local GDP per capita. Conclusion. The cost of investigation and treatment of nephroblastoma remains a challenge everywhere; but especially in Africa. However; it is a very cost-effective disease to treat and children in Africa should not be denied treatment


Subject(s)
Cost of Illness , Cost-Benefit Analysis , Guideline , Neoplasm Staging , Wilms Tumor/therapy
3.
Afr. j. paediatri. surg. (Online) ; 8(1): 49-56, 2011. ilus
Article in English | AIM | ID: biblio-1257540

ABSTRACT

Introduction: The challenge of management with bilateral Wilms' tumours is the eradication of the neoplasm; while at the same time preserving renal function. Surgical management with a variety of nephron-sparing techniques; combined with chemotherapy and occasionally supplemented by transplantation has evolved over the last 30 years to achieve remarkable success. We document the experience of a single centre in a developing country. Material and Methods: Twenty-three bilateral Wilms' tumours were seen in our service between 1981 and 2007. Treatment was; in most cases; according to National Wilms' Tumour Study Group protocols; with initial bilateral biopsy; neoadjuvant chemotherapy; and tumourectomy. Technique of nephrectomy included full mobilization of the tumour-involved kidney; topical cooling with slush ice; vascular exclusion; tumour resection and reconstruction of the remnant kidney. Results: Twelve patients are alive and free of disease one to 15 years after treatment; all with well-preserved renal function (lowest glomerular filtration rate was 65 ml/min per (1.73 m 2 ). None of the survivors have hypertension. Eleven have died (two of unrelated disease) including six of the seven with spread outside the kidney. All three with unfavourable histology are alive. Four of the five metachronous presentations are alive; as are eight of 12 patients with synchronous bilateral tumours who presented since 2000. Conclusions: Appropriate chemotherapy and nephron-sparing surgery can achieve good results with preservation of adequate renal function in nearly all cases. Unfavourable histology did not have a reduced survival in our series. Metastatic spread outside the kidney had a poor prognosis


Subject(s)
Nephrons , Organ Preservation , Surgical Procedures, Operative , Wilms Tumor/surgery , Wilms Tumor/therapy
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