Prenatal diagnosis of congenital mesoblastic nephroma
Obstetrics & Gynecology Science
;
: 405-408, 2015.
Artículo
en Inglés
| WPRIM
| ID: wpr-62650
ABSTRACT
Congenital mesoblastic nephroma is a rare renal tumor that is diagnosed during pregnancy and is associated with polyhydramnios, prematurity, and neonatal hypertension. Differential diagnoses include Wilms tumor, adrenal neuroblastoma, and other abdominal tumors. We report a case of congenital mesoblastic nephroma detected by prenatal ultrasonography as a large fetal renal mass with polyhydramnios at 32 weeks of gestation. Ultrasonography showed a 6x6-cm complex, solid, hyperechoic, round mass in the right kidney. At 35 weeks of gestation, the patient was admitted with preterm premature rupture of membranes and the baby was delivered vaginally. Postnatal ultrasonography and computed tomography showed a heterogeneous solid mass on the right kidney. At the end of the first week of life, a right nephrectomy was performed and subsequent pathological examination confirmed a cellular variant of congenital mesoblastic nephroma with a high mitotic count. Postoperative adjuvant chemotherapy was administered. The newborn was discharged in good condition.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Diagnóstico Prenatal
/
Rotura
/
Ultrasonografía Prenatal
/
Polihidramnios
/
Ultrasonografía
/
Quimioterapia Adyuvante
/
Nefroma Mesoblástico
/
Tumor de Wilms
/
Diagnóstico Diferencial
/
Quimioterapia
Tipo de estudio:
Estudio diagnóstico
Límite:
Humanos
/
Recién Nacido
/
Embarazo
Idioma:
Inglés
Revista:
Obstetrics & Gynecology Science
Año:
2015
Tipo del documento:
Artículo
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