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Adult Wilms Tumour in pregnancy

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dc.contributor.author Owen Mangusu, Amata Bryan, Oyaya Cyndy, Bitta caesar
dc.date.accessioned 2020-09-04T09:52:45Z
dc.date.available 2020-09-04T09:52:45Z
dc.date.issued 2020
dc.identifier.uri https://repository.maseno.ac.ke/handle/123456789/2734
dc.description https://www.ajol.info/index.php/eamj/article/view/194050 en_US
dc.description.abstract Wilms’ tumor (nephroblastoma) is the most common primary renal malignancy in children, with a peak presentation in the ages 3-4 years. Wilms’ tumor is extremely rare in adults with around 300 cases described in literature. This presents both a diagnostic and treatment challenge in adults due to lack of standard protocols. Herein, we report a case of a 28-year-old primigravida who underwent nephrectomy postpartum for presumed renal cell carcinoma that was diagnosed as Wilms’ tumor at histology. This case is being reported on account of its peculiar presentation, and its presentation in pregnancy, to provoke further research and thus improve management in the adult patient. en_US
dc.publisher AJOL en_US
dc.title Adult Wilms Tumour in pregnancy en_US
dc.type Article en_US


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