Disorders of the Fetomaternal Unit: Hematologic Manifestations in the Fetus and Neonate

被引：9

作者：

Black, L. Vandy ^{[3
]}

Maheshwari, Akhil ^{[1
,2
]}

机构：

[1] Univ Alabama Birmingham, Div Neonatol, Birmingham, AL 35233 USA

[2] Univ Alabama Birmingham, Div Pediat Gastroenterol, Birmingham, AL 35233 USA

[3] Univ Alabama Birmingham, Div Pediat Hematooncol, Birmingham, AL 35233 USA

来源：

SEMINARS IN PERINATOLOGY | 2009年 / 33卷 / 01期

关键词：

placenta; neutropenia; anemia; thrombocytopenia; G-CSF; LOW-BIRTH-WEIGHT; IDIOPATHIC THROMBOCYTOPENIC PURPURA; SEVERE GROWTH-RETARDATION; RHD HEMOLYTIC-DISEASE; HEALTH-CARE-SYSTEM; BLOOD-CELL COUNTS; ALLOIMMUNE THROMBOCYTOPENIA; RHESUS ALLOIMMUNIZATION; NUCLEATED ERYTHROCYTES; AUTOIMMUNE NEUTROPENIA;

D O I：

10.1053/j.semperi.2008.10.005

中图分类号：

R71 [妇产科学];

学科分类号：

100211 ;

摘要：

Histoarchitectural characteristics of the human placenta place the fetus at a high risk of growth restriction, abnormal fetomaternal cell traffic, and vertical transmission of pathogens. These abnormalities of the fetomaternal unit are frequently associated with hematological abnormalities in the fetus/neonate and may be the first, most common, or the only clinical manifestations of these conditions. This article reviews the pathophysiology and characteristic hematological manifestations of these conditions in the fetus and the neonate.

引用

页码：12 / 19

页数：8

共 78 条

[51]

Motta M, 2003, ARCH DIS CHILD-FETAL, V88, P341

[52] Haemolytic disease of the newborn [J].

Murray, Neil A. ;

Roberts, Irene A. G. .

ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2007, 92 (02) :F83-F88

[53] In vitro assessment of recombinant, mutant immunoglobulin G anti-D devoid of hemolytic activity for treatment of ongoing hemolytic disease of the fetus and newborn [J].

Nielsen, Leif K. ;

Green, Trine H. ;

Sandlie, Inger ;

Michaelsen, Terje E. ;

Dziegiel, Morten H. .

TRANSFUSION, 2008, 48 (01) :12-19

[54]

Ouellet Annie, 2004, Infect Dis Obstet Gynecol, V12, P23, DOI 10.1080/1064744042000210357

[55] Preeclampsia does not increase the risk for culture proven sepsis in very low birth weight infants [J].

Paul, DA ;

Leef, KH ;

Sciscione, A ;

Tuttle, DJ ;

Stefano, JL .

AMERICAN JOURNAL OF PERINATOLOGY, 1999, 16 (07) :365-372

[56] Insights into viral transmission at the uterine-placental interface [J].

Pereira, L ;

Maidji, E ;

McDonagh, S ;

Tabata, T .

TRENDS IN MICROBIOLOGY, 2005, 13 (04) :164-174

[57] INCREASED NUCLEATED RED BLOOD-CELL COUNTS IN SMALL FOR GESTATIONAL-AGE INFANTS WITH VERY LOW BIRTH-WEIGHT [J].

PHILIP, AGS ;

TITO, AM .

AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1989, 143 (02) :164-169

[58] ANTIBODIES TO HISTO-BLOOD GROUP SUBSTANCES-A AND SUBSTANCES-B - AGGLUTINATION TITERS, IG CLASS, AND IGG SUBCLASSES IN HEALTHY-PERSONS OF DIFFERENT AGE CATEGORIES [J].

RIEBEN, R ;

BUCHS, JP ;

FLUCKIGER, E ;

NYDEGGER, UE .

TRANSFUSION, 1991, 31 (07) :607-615

[59]

Robertson W B, 1985, Obstet Gynecol Annu, V14, P411

[60]

ROLLINS MD, 1993, BIOL NEONATE, V63, P147

← 1 2 3 4 5 6 7 8 →