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Polyorchidism is a rare congenital anomaly defined as the presence of supernumerary testes with the most common presentation with two homolateral and one contralateral testes. Since the first case reported in 1880; more than 100 cases were published in the literature [1]. Here we report a 37 year old case with left supernumerary testes presented with painless mass and had a medical history of infertility.
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