Placental diagnostic criteria and clinical correlation - A workshop report

被引:255
作者
Redline, RW [1 ]
Heller, D
Keating, S
Kingdom, J
机构
[1] Case Western Reserve Univ, Sch Med, Dept Pathol & Reprod Biol, Cleveland, OH 44106 USA
[2] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Pathol, Newark, NJ 07103 USA
[3] Univ Toronto, Mt Sinai Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5G 1X5, Canada
[4] Univ Toronto, Mt Sinai Hosp, Div Maternal Fetal Med, Toronto, ON M5G 1X5, Canada
关键词
placental pathology; IUGR; ultrasound; prematurity;
D O I
10.1016/j.placenta.2005.02.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Placental pathology is a valuable link explaining how underlying pregnancy risk factors result in adverse pregnancy outcome. This potentially useful information is currently underutilized due to a general lack of rigor in placental diagnosis. This lack of rigor is in large part due to a failure to appreciate the importance of the information provided and hence to demand accurate and clinically responsive reporting. This workshop reviewed the results of a recent initiative by the Perinatal Section of the Society for Pediatric Pathology to systematize and validate diagnostic schema for the description of lesions related to three important pathologic processes: amniotic fluid infection, maternal vascular underperfusion, and fetal vascular obstruction. This was followed by presentation of three studies correlating these pathologic processes with the following clinical outcomes: complications of prematurity, fetal growth restriction, and neurodisabillty following term delivery. © 2005 Published by IFPA and Elsevier Ltd.
引用
收藏
页码:S114 / S117
页数:4
相关论文
共 18 条
[1]  
ALTSHULER G, 1992, OBSTET GYNECOL, V79, P760
[2]   The Scottish perinatal neuropatholo study: clinicopathological correlation in early neonatal deaths [J].
Becher, JC ;
Bell, JE ;
Keeling, JW ;
McIntosh, N ;
Wyatt, B .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2004, 89 (05) :F399-F407
[3]   Origin and timing of brain lesions in term infants with neonatal encephalopathy [J].
Cowan, F ;
Rutherford, M ;
Groenendaal, F ;
Eken, P ;
Mercuri, E ;
Bydder, GM ;
Meiners, LC ;
Dubowitz, LMS ;
de Vries, LS .
LANCET, 2003, 361 (9359) :736-742
[4]   Antenatal mycoplasma infection, the fetal inflammatory response and cerebral white matter damage in very-low-birthweight infants [J].
Dammann, O ;
Allred, EN ;
Genest, DR ;
Kundsin, RB ;
Leviton, A .
PAEDIATRIC AND PERINATAL EPIDEMIOLOGY, 2003, 17 (01) :49-57
[5]  
Greenwood C, 2003, BJOG-INT J OBSTET GY, V110, P6
[6]   Changing panorama of cerebral palsy in Sweden. VIII. Prevalence and origin in the birth year period 1991-94 [J].
Hagberg, B ;
Hagberg, G ;
Beckung, E ;
Uvebrant, P .
ACTA PAEDIATRICA, 2001, 90 (03) :271-277
[7]  
Hansen A, 1998, PEDIATR RES, V43, P15
[8]   Very low birthweight placenta: Clustering of morphologic characteristics [J].
Hansen, AR ;
Collins, MH ;
Genest, D ;
Heller, D ;
Shen-Schwarz, S ;
Banagon, P ;
Allred, EN ;
Leviton, A .
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2000, 3 (05) :431-438
[9]   Very low birthweight infant's placenta and its relation to pregnancy and fetal characteristics [J].
Hansen, AR ;
Collins, MH ;
Genest, D ;
Heller, D ;
Schwarz, S ;
Banagon, P ;
Allred, EN ;
Leviton, A .
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2000, 3 (05) :419-430
[10]   Coagulation, inflammation, and the risk of neonatal white matter damage [J].
Leviton, A ;
Dammann, O .
PEDIATRIC RESEARCH, 2004, 55 (04) :541-545