Title of article :
Wilms’ Tumor: Histopathological Variants and the Outcomes of 31 Cases at a Tertiary Care Center in Northern India
Author/Authors :
Marwah Nisha نويسنده Department of Pathology, Pt. B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India , Bhutani Namita نويسنده Department of Pathology, Post Graduate Institute of Medical Sciences (PGIMS), Rohtak, Haryana, India , Kajal Pradeep نويسنده Department of Pediatric Surgery, PGIMS Rohtak, Haryana, India , Rattan Kamal Nain نويسنده Department of Pediatric Surgery, PGIMS Rohtak, Haryana, India
Issue Information :
فصلنامه با شماره پیاپی 31 سال 2017
Abstract :
Background: Wilms’ tumor is the most common malignant renal tumor in the
pediatric age group. This tumor is classically managed by multimodal treatment which
involves surgery, radiotherapy and chemotherapy. While there is plenty of data in
world literature on the outcome of Wilms’ tumor, there is a paucity of data from India.
Methods: All patients with proven diagnosis of Wilms’ tumor between 2008 to 2012
were noted from the hospital’s cancer registry. We performed detailed analyses of all
patients’ clinical case records for demographic profiles, clinical features, imaging
studies, treatment, and outcome. Histopathological classification of the tumor determined
the patient’s post-operative management. All patients were followed for a period of 3
years and we analyzed the eventual outcome in the form of disease-free survival,
complications, tumor recurrence, and mortality.
Results: There were 31 cases of Wilms’ tumor included in this study. The median
age of presentation was 3-4 years (range: 5 months-6 years) with a female: male ratio
of 1.2:1. Abdominal mass was the chief presenting feature in 20 (64.5%) patients
followed by abdominal pain in 6 (19.3%). All children had unilateral disease, 25
(80.6%) had right-sided and 6 (19.3%) had left-sided disease. Bilateral disease was seen
in only one case. Of the 31 cases of Wilms’ tumor, 36% cases presented with stages I
and II disease, 55% had stage III, and 9% of the cases were stage IV. Most cases of Wilms’
tumor were stage III. The majority had classical Wilms’ tumor with a favourable
histology. The estimated 5-year event free survival was 87.3%
Conclusion: A multidisciplinary approach can approach similar survival rates
compared to the National Wilms’ Tumor Study Group, even in the Indian scenario. Further
improvement in survival of these children can only be achieved by increasing awareness,
early recognition, appropriate referral, and a multidisciplinary approach.
Journal title :
Astroparticle Physics