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East and Central African Journal of Surgery
Association of Surgeons of East Africa and College of Surgeons of East Central and Southern Africa
ISSN: 1024-297X EISSN: 2073-9990
Vol. 13, Num. 1, 2008, pp. 60-65

East and Central African Journal of Surgery, Vol. 13, No. 1, March-April 2008, pp. 60-65

Paediatric Cancers at Butare University Teaching Hospital in Rwanda.

M. Makanga, M.A. Ayinkamiye, L.Ngendahayo,  I.Kakande

Butare UniversityTeaching Hospital, NUR, Rwanda
Correspondance to:Dr Makanga Martine,mail:mmaka1@yahoo.fr

Presented at Association of Surgeons of East Africa Conference in Mombasa, Kenya- Dec 6, 2007. 

Code Number: js08010

Background: Cancer is an important cause of mortality in many of the economically developed nations of the world. More than 10% of all deaths in children below 15 years of age are caused by malignant diseases in developed countries. In the developing world, childhood cancers are yet to be recognized as a major pediatric illness due to several other competing causes of death like diarrheal illness and respiratory illness. 
Methods: A descriptive retrospective study of children admitted for cancer in Butare Teaching Hospital over a 7 years period (January 1999-December 2005) was carried out The study population included 36 children aged 0-15 years admitted with cancer at Butare university teaching Hospital. Data was analyzed using Epi data, SPSS11,5  computer programs.
Results: The average age of our patients was 5.9 years with the youngest patient being 5 month old. The peak incidence of cancer was found in the 0-5 years age group and accounted for 21 patients (58, 3%). The Male to Female sex ratio was 1.7: 1. The most common types of cancer were: Burkett’s lymphoma, Non-Hodgkin Lymphoma and Hodgkin’s Lymphoma. Treatment included   surgery for 17 patients(47.2%), chemotherapy for 4 patients (11.1%),  surgery  combined  with  post-operative  chemotherapy for 1 patient (2.7%), the  association  of  pre-operative  chemotherapy + surgery + post-operative  chemotherapy  for 1 patient (2.7%)  and  palliative care for 13 patients (36.1%).  The average length of hospital stay was 36.6 days ranging   from 2 to 510   days.The hospital mortality rate was 27.7%.
Recommendation: The creation of an oncology department and a National cancer Register are recommended.

Introduction                

Although, Cancer is rare in children aged less than 15 years1, it represents a main concern for parents, families, and health professionals to care for children affected with cancer. The problems confronting Paediatric oncology in Africa are many. They are linked to:

  • Lack of common strategy and policies concerning detection, prevention, and treatment of cancer patients
  • Insufficient specialized human resources,
  • Absence of referral cancer centers,
  • Unavailability of antimitotic drugs and radiotherapy,
  • Lack of financial resources
  • Patients consulting at late stage of cancer.

These lead to low survival and cure rates: The patients’ survival at 5 years is ≤ 50% in developing world whereas cure rates in developed countries represent 75-80 %1. In Rwanda there is no possibility of effective, efficient management of cancer after diagnosis is confirmed for lack of an established oncology Department. A review of literature shows that no specific study on cancer in children has bee reported from Rwanda. It was with such background that a study was undertaken on childhood cancers in Butare university Teaching Hospital. 

Results

During 7 years period of our study, there were 20,171 admitted patients in the five departments of Paediatric, Surgery, ENT, Ophthalmology and Stomatology of whom 36 (0.18%)patients had childhood cancer. Table 1 shows the annual distribution of children with cancer in the 7 years. Figure 1 shows the age distribution. The age group 0 to 5 years was the most affected accounting for 21 (58.3%) of the cases. The youngest patient was aged 5 months ( Figure 1). Twenty three patients were males and 13 were females. (Male: female ratio = 1.8: 1). Table 2 shows the distribution of cancers according to age groups. The 0 – 5 year age group accounted for 21 (58.3%) of the cases. The commonest malignancy in this age group was Burkitt’s lymphoma. Burkitt‘s Lymphomas were accounted for a third (33.3%) of the tumours in the 0 – 5 age group (Table 2). The commonest type in the 6 – 10 years age group was non Hodgkin’s lymphoma. In males, Burkitt’s lymphoma accounted for 14 (60.9%) of cancers while in females the tumours were more evenly distributed (Table 3). Table 4 shows the location of the cancers. Most tumours were located in accessible sites for the guardians or patients as well as the health workers.

Clinical features on the 5 main cancers were many. A swelling or mass was the predominant presentation. Other features included pyrexia, peripheral lymphadenopathy, hepatomegaly, splenomegaly, weight loss, pallor and abdominal tenderness. Others signs and symptoms deferred  from one type of cancer to the other. The site of tumour varied. Burkitt’s lymphoma was located in maxilla and mandible (8 cases over 10:80%). Thirty four patients had confirmed histological diagnosis. Two patients had diagnosis confirmed by bone marrow examination.

Tables 6 and 7 summarize the mode of treatment received by the children. One form of surgery or the other was performed in 17 (47.2%) of the patients and included tumour excision, limb amputation, Nephrectomy, eye exenteration and others. Only 4 patients (11.1%) benefited from chemotherapy. Palliative treatment was offered to 13 patients with advanced disease. Palliative care included analgesics, intravenous fluids, blood transfusion, and nursing. Radiotherapy is not offered in Rwanda and therefore none of the patients had such a modality of treatment. Only 4 patients had chemotherapy. Two patients with NHML received a combination of Endoxan 40mg /m2 + Vincristine + Methotrexate + Prednisolone for 2 sessions.  One patient with Burkitt’s Lymphomareceived 3 sessions of Endoxan 40mg/m2 and Prednisolone 2mg/ kg. One patient with Acute Lymphoïd  Leukemia had Endoxan 40mg/m2 + Vincristine1,5mg/m2 + L-Asparaginase+ Methotrexate + Prednisolone 2 mg/kg.

The average length of stay in hospital was 36.6% days with the extremes of 2 days and 510 days.

Table 1. Patients’ Distribution According to Years of Admission.

Year

Department

Total

Surgery

Paediatric

ENT

Ophthalmology

Stomatology

1999

2

 

1

 

0

 

0

 

0

 

3

 

2000

0

 

0

 

2

 

2

 

0

 

4

 

2001

2

 

5

3

 

0

 

0

 

10

 

2002

1

 

3

 

1

 

1

 

0

 

6

 

200 3

0

 

2

 

2

 

0

 

0

 

4

 

2004

1

 

1

 

1

 

0

 

0

 

3

 

2005

1

 

2

 

2

 

0

 

1

 

6

 

Total

7

 

14

 

11

 

3

 

1

 

36

 

Table 2.  Age Distribution and type of cancer. 

Type  of cancer

Age group (years)

Total

0 to 5

6 to 10

11 to 15

*NHL

0

6

1

7

Burkitt’s Lymphoma

7

3

0

10

Hodgkin’s Lymphoma

2

0

2

4

Retinoblastoma

2

0

0

2

Rhabdomyosarcoma

2

0

0

2

Nephroblastoma

2

0

0

2

Neuroblastoma

1

0

0

1

Osteosarcoma

0

0

1

1

Non-specified Sarcoma

1

0

0

1

Malignant Schwanoma

1

0

0

1

Hepatoblastoma

1

0

0

1

Malignant Mélanoma

0

1

0

1

**AcLL

2

0

1

3

Total

21

10

5

36

*NHL = Non Hodgkin Lymphoma,    **Ac LL = Acute Lymphoïd Leukemia

Table 3.  Patient Distribution According to Type of Cancer and Sex.

Type of cancer

Sex

Total

M :F Sex Ratio

Male

Female

*NHL

6

1

7

6 :1

Burkitt’Lymphoma

8

2

10

4 :1

Hodgkin’sLymphoma

3

1

4

3 :1

Retinoblastoma

0

2

2

0 :2

Rhabdomyosarcoma

1

1

2

1 :1

Nephroblastoma

1

1

2

1 :1

Neuroblastoma

1

0

1

1 :0

Osteosarcoma

0

1

1

0 :1

Non-specified Sarcoma

0

1

1

0 :1

Malignant Schwanoma

0

1

1

0 :1

Hepatoblastoma

0

1

1

0 :1

Malignant Melanoma

1

0

1

1 :0

**Ac LL

2

1

3

2 :1

Total

23

13

36

1.8 :1

*NHL = Non Hodgkin Lymphoma,    **Ac LL = Acute Lymphocytic Leukemia

Patients’ complications were: infection, bonemarrow aplasia, blindness, nausea, vomiting,  observed in 4 (27.7%) patients who had Burkiitt’s Lymphoma, acute leukemia or Hodgkin lymphoma under chemotherapy.

The outcome at discharge varied: 11 patients (30.5%) improved, 15 patients (41.6%) didn’t improve that is general state remained the same or worsened. Ten patients died in hospital (27.8% mortality) and included 1 patient who had surgery, all 4 patients treated with chemotherapy  and 5 patients managed with palliative care alone. The patients’ follow up was difficult, only 3 patients over 36 was seen 1 month later.

Table 4. Sites of Cancers.

Type of cancer

Site  of  Tumour

Number

Burkitt’Lymphoma

Retro-auricular

1

Abdominal (right kidney)

1

Supra maxillar

6

Mandibular

2

Total

10

NHL

Supra maxillar

2

Right tibia

1

Cervical nodes

2

Buccal cavity

1

Mandibular

1

Total

7

Hodgkin’ Lymphoma

Neck lymphonodes

4/4

Rhabdomyosarcoma

Cervical

1

bladder 

1

Total

2

Nephroblastoma

Right kidney

2/2

Retinoblastoma

Right eye

1

Left   eye

1

Total

2

Table 5. Histological Types of Cancer in Children

Type of Cancer

 

Number

 

%

NHL

7

19.4

Burkitt’s Lymphoma

10

27.7

Hodgkin’s Lymphoma

4

11.1

Retinoblastoma

2

5.5

Rhabdomyosarcoma

2

5.5

Nephroblastoma

2

5.5

Neuroblastoma

1

2.7

Osteosarcoma

1

2.7

Non identified Sarcoma

1

2.7

Malignant Schwanoma

1

2.7

Hepatoblastoma

1

2.7

Malignant Melanoma

1

2.7

Acute Lymphoid Leukemia

3

8.3

Total

36

100

Table 6. Patients Distribution According Treatment 

Treatment

 

Number

 

%

Surgery

Tumor excision

12

33.3

Limb amputation

1

2.7

Nephrectomy

2

5 .5

Eye exenteration

2

5.5

Chemotherapy

Cyclophosphamide+Vincristine+Methotrexate +

Prednisolone

2

5.5

Cyclophosphamide+Prednisolone

1

2.7

Cyclophοsphamide + Vincristine+L-Asparaginase + Methotrexate + Prednisolone    

1

2.7

Surgery Chemotherapy

Limb amputation+Cyclophοsphamide+ Vincristine + Prednisolone      in   post-operative

1

2.7

Palliative traitement

Analgesics, ATB, intravenous fluids, blood  transfusion, antipyretics,  etc.

13

36.1

Chemotherapy-Surgery-Chemotherapy

Cyclophosphamide + Vincristine+Prednisolone + Nephrectomy+ Cyclophosphamide + Vincristine + Adriblastine + Prednisolone.

1

2.7

Total

 

36

 

100

Tableau 7. Patients  outcome versus type of cancer

Type of cancer

Total

Improved

No Improvement

Died in hospital

Total

*NHL

2

3

2

7

Burkitt’s Lymphoma

1

7

2

10

**HL

1

2

1

4

Acute leukemia

0

0

3

3

Retinoblastoma

2

0

0

2

Rhabdomyosarcoma

0

1

1

2

Nephroblastoma

2

0

0

2

Others

3

2

1

6

Neuroblastoma

1

0

0

1

Total

 

11

 

15

 

10

 

36

  *NHL = Non Hodgkin’s Lymphoma                 **HL = Hodgkin’s Lymphoma

Discussion

Cancer is a subject of constant preoccupation in the world1. It is rare in children aged less than 15 years, it represents 1-3% of all tumors in the population2,3,4,5,6,7. In France, each year 1800 to 2000 new cases of cancer in children are registered1,3,8. In Switzerland, 220 children; in Belgium less than 300 children are affected each year. This study confirmed that cancer in children is a rare . Our hospital prevalence was similar to that reported by other sauthors3,5,6,9. The disease predominantly affects young children in the 0 -5 years age group. Other studies have reported similar findings.1,2,6.

The clinical presentation in our children  was in agreement with previous literature10,3,7,11,12. The patients’ management and outcome in our series significantly differed from what is reported by other centres with established surgical oncology departments1,3,5,13. In our study, surgical treatment, being the only available form of treatment for cancer in the country, was offered to many cases.. Antimitotics drugs were not always available, and they were too expensive for  ordinary Rwandese patients. There is no Radiotherapy Centre in the country nor is there any well established chemotherapy unit. This unfortunate situation contributed to the poor outcome and bad prognosis of our patients. The need for establishing such centres in the country is overwhelming.

Conclusion

Our findings showed that the clinical features and pathological types of cancersseen among children in Rwanda were similar to what has been reported by other authors in the literature. But the difference was that most of our patients were admitted in advanced stage of the disease. Because of lack of an Oncology Department, absence of appropriate drugs for chemotherapy, and lack of radiotherapy and palliative Medicine,  our patients’ management and outcome were poor. There is an urgent need to improve our Hospital in establishing proper structure and facilities to attend to cancer patients efficiently. 

Recommendations

  • We appeal to the Ministry of Health to establish an oncology department in Rwanda and to ensure that chemotherapy, radiotherapy, palliative medicine and counseling sevices for patients affected with cancer are available.
  • A national cancer register should be opened.
  • Personnel should be trained to form multidisciplinary teams and specialists for the care of cancer patients.
  • Diagnostic facilities for cancer should be improved to make diagnosis of cancer quick and accurate.                                         

References

  1. Desandes.E. ,Clavel.J.,Berger.C.,Bernard.J.L.,Blouin.P.,Lumley.L.et al.  Incidence des cancers de l’enfant en France, 1990-1999.Bulletin épidémiologique hebdomadaire2005, 32,161-4.
  2. Les tumeurs solides malignes de l`enfant à Brazzaville : Aspects épidémiologiques et anatomopathologiques. http://WWW. Pathexo.Fr/pdf/2004.2/T97-2-2511-2p.pdf
  3. Dominique Plantaz : Particularités épidémiologiques des cancers chez  l’enfant.Faculté de Médecine de Grenoble, Décembre, 2003.
  4. Le cancer chez l’enfant.http://www.esante.be/be/magazine_sante/sante_enfants_adolescents/cancer_enfant-6108-971-art.htm
  5. Anne d’Andon,  Gilles Vassal, Olivier Hartmann. Les tumeurs osseuses.Institut Gustave-Roussy, Février, 2004.
  6. Laila Hessissen :Le traitement du cancer chez l'enfant. Rabat, Novembre2001.
  7. Le cancer de l`enfant. http:// WWW.ands.dz/sacp/donnees/onco002.htm
  8. Les cancers  chez l`enfant. http://WWW.la-sfop.com/sfop.nsf/pgLCE?Openpage&AutoFramed
  9. Phillipe Abimelec. Médecine et chirurgie de la peau, des ongles et des cheveux, Novembre 2000.
  10. J’ai  vaincu le cancer.http://www.UICC.org/fileadmin/aser-uploadUICC/wcd/leafletA4-fr.pdf
  11. Baruchel.A ; Benkritly.A ;Benzohra.A ;Caulin.C ;Chastagner.P ;Defrance.R ;et al. Hémato-cancérologie pédiatrique. Table Ronde no4.Giens 2002.
  12. Outtara.K., Daffes.,Tembely.Y.A.  Les tumeurs du  rein dans la pratique de   l’’urologue au Mali. (A propos de 17 cas).Médecine d’Afrique Noire1993, 40(4),253-6
  13. KA. A.S, Imbert. P., Moreira. C.  et al: Epidémiologie et pronostic des affections malignes de l`enfant2003, 63, 521-26.

© 2008 East and Central African Journal of Surgery


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