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1.
Obstet Gynecol ; 107(2 Pt 2): 463-6, 2006 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-16449150

RESUMEN

BACKGROUND: Placental abscess formation is rarely recognized prenatally. We present a case detected ultrasonographically that developed from a central line infection and caused recurrent maternal bacteremia. CASE: A young woman with a 21-week twin gestation presented with recurrent fevers. She had received treatment for bacteremia due to Serratia marcescens. The initial source of the infection was a peripherally inserted central catheter line placed in the first trimester for hyperemesis gravidarum. Fevers continued throughout the second course of antibiotics. An abscess seen sonographically in twin A's placenta was aspirated using a spinal needle, revealing Serratia bacteria. Aspiration was performed at 22 weeks of gestation. Amniotic fluid samples obtained from both sacs were negative for infection. Over 4 weeks, the abscess enlarged and she was delivered. Twin A died of sepsis and twin B had a relatively favorable neonatal course. CONCLUSION: Prenatal diagnosis of placental abscess presents a difficult management dilemma. Traditional amniotic fluid studies did not predict the poor outcome of the affected fetus.


Asunto(s)
Absceso/diagnóstico por imagen , Bacteriemia/etiología , Enfermedades Placentarias/diagnóstico por imagen , Complicaciones Infecciosas del Embarazo/diagnóstico por imagen , Embarazo Múltiple , Infecciones por Serratia/diagnóstico por imagen , Serratia marcescens , Ultrasonografía Prenatal , Absceso/complicaciones , Adulto , Femenino , Humanos , Embarazo , Recurrencia , Infecciones por Serratia/complicaciones
2.
Am J Obstet Gynecol ; 187(6): 1679-85, 2002 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-12501083

RESUMEN

OBJECTIVE: It has been suggested that there is a decrease in the collagen content of the fetal membranes when there is premature rupture of the membranes before the onset of labor. This study was designed to determine whether decreased amniochorion collagen production (as measured by reduced amounts of messenger RNA) or alterations in relative production of different fibrillar and nonfibrillar collagens are associated with premature rupture of the membranes. STUDY DESIGN: Fetal membranes were collected after preterm (24-36 weeks of gestation) and term (> or =37 weeks of gestation) deliveries both with and without premature rupture of the membranes. Specimens with evidence of histologic chorioamnionitis were excluded. The messenger RNA levels for fibrillar collagen types I, III, and V and fibril-associated collagens with interrupted triple-helices types XII and XIV were measured with relative quantitative reverse transcriptase-polymerase chain reaction. RESULTS: The messenger RNA levels for fibrillar collagens decreased with advancing gestational age. Preterm premature rupture of membranes was associated with increased messenger RNA levels for fibrillar collagens and fibril-associated collagens with interrupted triple-helices collagen XII, but not type XIV. The greatest change in relative amounts of collagen messsenger RNA was demonstrated by an increased type I/XIV ratio, which was due to the up-regulation of type I levels, but not type XIV levels. CONCLUSION: A rise in fibrillar collagen production (messenger RNA) for types I, III, and V and fibril-associated collagens with interrupted triple-helices collagen type XII is observed with preterm premature rupture of the membranes. There is no evidence for a similar up-regulation of messenger RNA for fibril-associated collagens with interrupted triple-helices collagen type XIV. The rise in the collagen I/XIV messenger RNA ratio in preterm premature rupture of the membranes may result in collagen fibrils without enough stabilizing fibril-associated collagens with interrupted triple-helices type XIV on the fibril surface to maintain structural integrity.


Asunto(s)
Amnios/química , Corion/química , Colágeno/genética , Rotura Prematura de Membranas Fetales/metabolismo , Expresión Génica , ARN Mensajero/análisis , Colágeno/metabolismo , Colágeno Tipo I/genética , Colágeno Tipo III/genética , Colágeno Tipo V/genética , Colágeno Tipo XII/análisis , Colágeno Tipo XII/genética , Femenino , Colágenos Asociados a Fibrillas/genética , Técnica del Anticuerpo Fluorescente , Edad Gestacional , Glicoproteínas/genética , Glicoproteínas/metabolismo , Humanos , Inmunohistoquímica , Embarazo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
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