Hidropesía fetal secundario a hemangioma cavernoso y síndrome polimalformativo / Fetal hydrops secondary to cavernous hemangioma and polymalformation syndrome
Prog. obstet. ginecol. (Ed. impr.)
; 54(5): 252-256, mayo 2011. ilus, graf
Article
in Es
| IBECS
| ID: ibc-142946
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
Presentamos un caso de hidropesía fetal no inmunitaria diagnosticada en la semana 32 de embarazo que finalizó con defunción fetal. Tras la necropsia se comprobó la coexistencia de un síndrome malformativo no filiado junto a la existencia de una tumoración hepática que invadía la cavidad torácica. Analizamos la posible asociación causal de ambos hallazgos (AU)
ABSTRACT
We report a case of non-immune fetal hydrops diagnosed at 32 weeks of pregnancy that ended in foetal death. Following the autopsy an unknown malformation syndrome was found together with a liver tumour that invaded the chest cavity. We analyse the possible causal association of both findings (AU)
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Collection:
06-national
/
ES
Database:
IBECS
Main subject:
Hydrops Fetalis
/
Polyhydramnios
/
Gastroschisis
/
Hemangioma, Cavernous
/
Lupus Erythematosus, Systemic
Type of study:
Diagnostic_studies
Limits:
Female
/
Humans
/
Pregnancy
Language:
Es
Journal:
Prog. obstet. ginecol. (Ed. impr.)
Year:
2011
Document type:
Article