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J Pediatr Hematol Oncol ; 38(6): e191-2, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-27322716

RESUMO

A male preterm infant was born with dysmorphic features consistent with Rubinstein-Taybi syndrome (RTS). An undescended right testicle was noted on examination. At 5 months of age he developed a palpable right-sided abdominal mass and an elevated alpha-fetoprotein. Histology revealed a malignant germ cell neoplasm arising within the undescended testis. This is the first reported case of a germ cell tumor occurring in a pediatric patient with RTS. Urologic abnormalities occur in approximately 52% of RTS patients, of which cryptorchidism is the commonest. Given the frequency of undescended testes in this population, closer screening may be warranted.


Assuntos
Criptorquidismo/complicações , Neoplasias Embrionárias de Células Germinativas/patologia , Síndrome de Rubinstein-Taybi/complicações , Neoplasias Testiculares/patologia , Humanos , Lactente , Masculino , Neoplasias Embrionárias de Células Germinativas/cirurgia , Neoplasias Testiculares/cirurgia
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