Morales L, Rovira J, Mongard M, Baeta E, Querol F X
J Urol. 1981 Aug;126(2):249-50. doi: 10.1016/s0022-5347(17)54463-8.
We describe a case of a solitary pelvic kidney coexisting with adrenal and pelvic neuroblastoma in a child with multiple malformations, including microcephaly, hypertelorism, aortic coarctation and a bifid uterus. The association of a solitary kidney and neuroblastoma has not been reported previously.
我们描述了一例患有多种畸形(包括小头畸形、眼距过宽、主动脉缩窄和双子宫)的儿童,其孤立性盆腔肾与肾上腺及盆腔神经母细胞瘤并存。孤立肾与神经母细胞瘤的关联此前尚未见报道。