RESUMEN
Congenital parvovirus B19 infection is a rare but serious condition that can result in hydrops fetalis and fetal death. Due to the virus' cytotoxic effect on fetal red blood cell precursors, postnatal infection can cause a neonatal viremia and secondary pure red cell aplasia. Here, we describe a case of congenital parvovirus infection in a preterm infant complicated by hydrops fetalis and chronic anaemia that responded to postnatal treatment with intravenous immunoglobulin administered on day of life 44. After treatment, the anaemia resolved as the neonate exhibited interval increases in haemoglobin, haematocrit and reticulocyte count with no subsequent need for red blood cell transfusions.
Asunto(s)
Anemia/terapia , Inmunoglobulinas Intravenosas/administración & dosificación , Infecciones por Parvoviridae/tratamiento farmacológico , Parvovirus B19 Humano/aislamiento & purificación , Complicaciones Infecciosas del Embarazo/diagnóstico , Adulto , Anemia/sangre , Anemia/virología , Anticuerpos Antivirales/sangre , Anticuerpos Antivirales/inmunología , Cordocentesis , Ecocardiografía , Transfusión de Eritrocitos , Femenino , Sangre Fetal/virología , Rotura Prematura de Membranas Fetales/virología , Feto/diagnóstico por imagen , Feto/virología , Humanos , Hidropesía Fetal/sangre , Hidropesía Fetal/diagnóstico , Hidropesía Fetal/terapia , Hidropesía Fetal/virología , Inmunoglobulina M/sangre , Inmunoglobulina M/inmunología , Recién Nacido , Recien Nacido Prematuro , Transmisión Vertical de Enfermedad Infecciosa , Masculino , Infecciones por Parvoviridae/complicaciones , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/transmisión , Parvovirus B19 Humano/inmunología , Polihidramnios/diagnóstico , Polihidramnios/virología , Embarazo , Complicaciones Infecciosas del Embarazo/virología , Resultado del Tratamiento , Ultrasonografía PrenatalRESUMEN
Parvovirus B19 (B19V) infection is well known for its mild, self-limiting clinical presentations in children, such as erythema infectiosum. Approximately 40% of women of childbearing age are susceptible to B19V infection. While maternal B19V infection usually has a good prognosis, B19V can cause severe fetal anaemia and pregnancy loss due to its ability to suppress erythroid progenitor cells. Non-invasive ultrasound monitoring for fetal anaemia is usually performed if maternal seroconversion occurs in the first 20 weeks of gestation, with amniocentesis for fetal infection reserved for those who first present with fetal anaemia or hydrops of unknown cause. Intrauterine transfusion is the standard treatment for severe fetal anaemia and is associated with a significant improvement in survival. However, survivors of hydrops fetalis may have a higher rate of long-term neurodevelopmental complications compared with non-hydropic survivors. This review aims to synthesise published data on the diagnosis, surveillance and outcomes of congenital parvovirus infection to assist clinicians in diagnosing and managing this important condition.
Asunto(s)
Terapias Fetales/métodos , Infecciones por Parvoviridae/congénito , Parvovirus B19 Humano , Complicaciones Infecciosas del Embarazo , Diagnóstico Prenatal/métodos , Femenino , Humanos , Recién Nacido , Transmisión Vertical de Enfermedad Infecciosa , Infecciones por Parvoviridae/diagnóstico , Infecciones por Parvoviridae/terapia , Infecciones por Parvoviridae/transmisión , Parvovirus B19 Humano/aislamiento & purificación , Embarazo , Complicaciones Infecciosas del Embarazo/diagnóstico , Complicaciones Infecciosas del Embarazo/terapia , Resultado del EmbarazoRESUMEN
Abstract Objective To investigate the clinical and sonographic parameters associated with adverse fetal outcomes in patients with congenital parvovirus B19 infection managed by intrauterine transfusion. Methods This was a single-center retrospective study conducted from January 2005 to December 2016 that assessed patients with singleton pregnancies with fetal parvovirus infection confirmed by a polymerase chain reaction of the amniotic fluid or fetal blood samples who underwent at least one intrauterine transfusion. The maternal characteristics, sonographic findings and parameters related to intrauterine transfusion were compared between the two groups (recovery/non-recovery), who were categorized based on fetal response after in-utero transfusions. Progression to fetal death or delivery without fetal recovery after the transfusions was considered nonrecovery and categorized as an adverse outcome. Results The final analysis included ten singleton pregnancies: seven of which were categorized into the recovery group and three of which into the non-recovery group. The baseline characteristics were similar between the groups. All fetuses were hydropic at the time of diagnosis. No significant differences related to sonographic or intrauterine transfusion parameters were identified between the groups; however, the nonrecovery group tended to have an increased number of sonographic markers and lower fetal hemoglobin and platelet levels before the transfusion. Conclusion We were unable to firmly establish the clinical or sonographic parameters associated with adverse fetal outcomes in patients with parvovirus infection managed with intrauterine transfusions; however, edema, placental thickening and oligohydramnios may indicate greater fetal compromise and, subsequently, adverse outcomes. However, further studies are necessary, mainly due to the small number of cases analyzed in the present study.
Resumo Objetivo Investigar os parâmetros clínicos e ultrassonográficos associados ao desfecho fetal adverso em pacientes com infecção congênita por parvovírus B19 manejada por meio de transfusão intrauterina. Métodos Trata-se de um estudo retrospectivo de um único centro realizado entre janeiro de 2005 e dezembro de 2016, que avaliou pacientes com gestação única com infecção fetal por parvovírus confirmada por reação em cadeia da polimerase de líquido amniótico ou amostras de sangue fetal submetidas a pelo menos uma transfusão intrauterina. As características maternas, os achados ultrassonográficos e os parâmetros relacionados à transfusão intrauterina foram comparados entre os dois grupos (recuperação/não recuperação), que foram categorizados com base na resposta fetal após transfusão intrauterina. A progressão para morte fetal ou parto sem recuperação fetal após transfusões foi considerada não recuperação, e categorizada como um desfecho adverso. Resultados A análise final incluiu dez gravidezes únicas: sete foram categorizadas no grupo de recuperação, e três, no grupo de não recuperação. As características basais foram semelhantes entre os grupos. Todos os fetos estavam hidrópicos no momento do diagnóstico. Não foram identificadas diferenças significativas entre os grupos em relação aos parâmetros ultrassonográficos ou os das transfusões intrauterinas; Entretanto, o grupo de não recuperação tendeu a ter um número aumentado demarcadores ultrassonográficos e níveis mais baixos de hemoglobina e plaquetas fetais antes da transfusão. Conclusão Não foi possível estabelecer firmemente os parâmetros clínicos ou ultrassonográficos associados ao desfecho fetal adverso em pacientes com infecção por parvovírus manejada por meio de transfusões intrauterinas. Entretanto, edema de pele, espessamento placentário e oligoidrâmnio podem indicar maior comprometimento fetal e, posteriormente, desfechos fetais adversos. No entanto, estudos adicionais são necessários, principalmente devido ao pequeno número de casos analisados neste estudo.
Asunto(s)
Humanos , Femenino , Embarazo , Adolescente , Adulto , Adulto Joven , Parvovirus B19 Humano , Infecciones por Parvoviridae/congénito , Enfermedades Fetales/virología , Pronóstico , Estudios Retrospectivos , Ultrasonografía Prenatal , Infecciones por Parvoviridae/diagnóstico por imagen , Enfermedades Fetales/diagnóstico por imagenRESUMEN
Objective To investigate the clinical and sonographic parameters associated with adverse fetal outcomes in patients with congenital parvovirus B19 infection managed by intrauterine transfusion. Methods This was a single-center retrospective study conducted from January 2005 to December 2016 that assessed patients with singleton pregnancies with fetal parvovirus infection confirmed by a polymerase chain reaction of the amniotic fluid or fetal blood samples who underwent at least one intrauterine transfusion. The maternal characteristics, sonographic findings and parameters related to intrauterine transfusion were compared between the two groups (recovery/non-recovery), who were categorized based on fetal response after in-utero transfusions. Progression to fetal death or delivery without fetal recovery after the transfusions was considered non-recovery and categorized as an adverse outcome. Results The final analysis included ten singleton pregnancies: seven of which were categorized into the recovery group and three of which into the non-recovery group. The baseline characteristics were similar between the groups. All fetuses were hydropic at the time of diagnosis. No significant differences related to sonographic or intrauterine transfusion parameters were identified between the groups; however, the non-recovery group tended to have an increased number of sonographic markers and lower fetal hemoglobin and platelet levels before the transfusion. Conclusion We were unable to firmly establish the clinical or sonographic parameters associated with adverse fetal outcomes in patients with parvovirus infection managed with intrauterine transfusions; however, edema, placental thickening and oligohydramnios may indicate greater fetal compromise and, subsequently, adverse outcomes. However, further studies are necessary, mainly due to the small number of cases analyzed in the present study.
Objetivo Investigar os parâmetros clínicos e ultrassonográficos associados ao desfecho fetal adverso em pacientes com infecção congênita por parvovírus B19 manejada por meio de transfusão intrauterina. Métodos Trata-se de um estudo retrospectivo de um único centro realizado entre janeiro de 2005 e dezembro de 2016, que avaliou pacientes com gestação única com infecção fetal por parvovírus confirmada por reação em cadeia da polimerase de líquido amniótico ou amostras de sangue fetal submetidas a pelo menos uma transfusão intrauterina. As características maternas, os achados ultrassonográficos e os parâmetros relacionados à transfusão intrauterina foram comparados entre os dois grupos (recuperação/não recuperação), que foram categorizados com base na resposta fetal após transfusão intrauterina. A progressão para morte fetal ou parto sem recuperação fetal após transfusões foi considerada não recuperação, e categorizada como um desfecho adverso. Resultados A análise final incluiu dez gravidezes únicas: sete foram categorizadas no grupo de recuperação, e três, no grupo de não recuperação. As características basais foram semelhantes entre os grupos. Todos os fetos estavam hidrópicos no momento do diagnóstico. Não foram identificadas diferenças significativas entre os grupos em relação aos parâmetros ultrassonográficos ou os das transfusões intrauterinas; Entretanto, o grupo de não recuperação tendeu a ter um número aumentado de marcadores ultrassonográficos e níveis mais baixos de hemoglobina e plaquetas fetais antes da transfusão. Conclusão Não foi possível estabelecer firmemente os parâmetros clínicos ou ultrassonográficos associados ao desfecho fetal adverso em pacientes com infecção por parvovírus manejada por meio de transfusões intrauterinas. Entretanto, edema de pele, espessamento placentário e oligoidrâmnio podem indicar maior comprometimento fetal e, posteriormente, desfechos fetais adversos. No entanto, estudos adicionais são necessários, principalmente devido ao pequeno número de casos analisados neste estudo.
Asunto(s)
Enfermedades Fetales/virología , Infecciones por Parvoviridae/congénito , Parvovirus B19 Humano , Adolescente , Adulto , Femenino , Enfermedades Fetales/diagnóstico por imagen , Humanos , Infecciones por Parvoviridae/diagnóstico por imagen , Embarazo , Pronóstico , Estudios Retrospectivos , Ultrasonografía Prenatal , Adulto JovenRESUMEN
We report a case of fetal cerebellar hemorrhage and hypoplasia, identified by fetal MRI after intrauterine blood transfusion at 21 weeks' gestation for treatment of severe anemia due to congenital Parvovirus infection. Postnatal MRI confirmed atrophy of bilateral cerebellar hemispheres and inferior vermis. Cerebellar capillaries may be extremely susceptible to hemodynamic changes in the setting of intrauterine blood transfusion due to severe anemia. Although the correlation between fetal intracranial anomalies and Parvovirus infection remains unclear, in this population, a detailed evaluation of the brain parenchyma should be considered prior to and after intrauterine blood transfusion.
Asunto(s)
Anemia/virología , Cerebelo/anomalías , Enfermedades Fetales/virología , Hemorragias Intracraneales/virología , Malformaciones del Sistema Nervioso/virología , Infecciones por Parvoviridae/congénito , Adulto , Anemia/terapia , Transfusión de Sangre Intrauterina , Cerebelo/diagnóstico por imagen , Cerebelo/virología , Discapacidades del Desarrollo/diagnóstico por imagen , Discapacidades del Desarrollo/virología , Imagen de Difusión por Resonancia Magnética , Femenino , Enfermedades Fetales/diagnóstico por imagen , Humanos , Hemorragias Intracraneales/diagnóstico por imagen , Malformaciones del Sistema Nervioso/diagnóstico por imagen , Infecciones por Parvoviridae/complicaciones , Infecciones por Parvoviridae/diagnóstico por imagen , EmbarazoAsunto(s)
Infecciones por Parvoviridae , Parvovirus , Aborto Espontáneo , Femenino , Humanos , Masculino , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/diagnóstico , Infecciones por Parvoviridae/fisiopatología , Embarazo , Segundo Trimestre del Embarazo , Estudios Retrospectivos , MortinatoRESUMEN
OBJECTIVE: The aim of this study was to evaluate the rate of women with polyhydramnios who eventually screened positive to infectious disease by serum screening testing for TORCH and parvovirus B19. METHODS: This is a retrospective observational study on singleton pregnancies with a diagnosis of polyhydramnios and who had serum screening for TORCH and parvovirus B19. Patients were followed with serial ultrasounds between 2006 and 2013. Maternal characteristics, medical and obstetric history were reviewed. Ultrasound parameters, including amniotic fluid index and fetal anomalies, and the results of serologic tests were reviewed. RESULTS: Two hundred ninety patients met the inclusion criteria. Of these, 56 (19%) presented one of the following pathological conditions associated with polyhydramnios: diabetes (13% of total cases), obstructive gastrointestinal lesions (5%), Rhesus isoimmunization (0.3%), chromosomal abnormalities or genetic syndromes (1%). Among the remaining 234 patients, only three had a positive test result for infectious disease (1%, 95% Confidence Interval (CI) 0-4%): two women were positive for parvovirus B19 and one for toxoplasmosis infection. In none of them the fetus was affected, as confirmed by serum testing after birth and by 3 years follow-up. CONCLUSIONS: Infectious disease screening does not seem beneficial in pregnancies with isolated polyhydramnios.
Asunto(s)
Infecciones por Citomegalovirus/epidemiología , Herpes Simple/epidemiología , Parvovirus B19 Humano/aislamiento & purificación , Polihidramnios/epidemiología , Complicaciones Infecciosas del Embarazo/epidemiología , Síndrome de Rubéola Congénita/epidemiología , Toxoplasmosis Congénita/epidemiología , Adulto , Infecciones por Citomegalovirus/congénito , Infecciones por Citomegalovirus/virología , Femenino , Herpes Simple/congénito , Herpes Simple/virología , Humanos , Recién Nacido , Italia/epidemiología , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/epidemiología , Polihidramnios/virología , Embarazo , Complicaciones Infecciosas del Embarazo/virología , Diagnóstico Prenatal/métodos , Diagnóstico Prenatal/estadística & datos numéricos , Prevalencia , Estudios Retrospectivos , Síndrome de Rubéola Congénita/virología , Toxoplasmosis Congénita/virologíaRESUMEN
UNLABELLED: We report the course of dicygotic twins born preterm after 29 (4)/7 weeks of gestation due to congenital Parvovirus B19 infection causing fetal hydrops with severe anemia in one infant in whom intrauterine transfusion was impossible to perform and high levels of viremia in both infants. After being discharged, they were readmitted at 3 months of age with critical aplastic crisis. Therapy with intravenous immunoglobulin infusion resulted in decreasing viremia followed by stable hemoglobin levels in both infants. CONCLUSION: Intravenous immunoglobulin treatment of congenital pure red cell aplasia due to Parvovirus B19 infection in preterm infants seems to be effective to introduce viral remission and to normalize erythropoiesis.
Asunto(s)
ADN Viral/análisis , Enfermedades en Gemelos/tratamiento farmacológico , Inmunoglobulinas Intravenosas/administración & dosificación , Infecciones por Parvoviridae/congénito , Parvovirus B19 Humano/genética , Aplasia Pura de Células Rojas/tratamiento farmacológico , Gemelos Dicigóticos , Enfermedades en Gemelos/sangre , Enfermedades en Gemelos/virología , Relación Dosis-Respuesta a Droga , Femenino , Humanos , Factores Inmunológicos/administración & dosificación , Recién Nacido , Masculino , Infecciones por Parvoviridae/sangre , Infecciones por Parvoviridae/virología , Aplasia Pura de Células Rojas/sangre , Aplasia Pura de Células Rojas/etiología , Inducción de RemisiónRESUMEN
OBJECTIVE: To study the role of asymptomatic maternal parvo B19 infection in severe fetal outcome in Province of Vojvodina. METHODS: One hundred seventy-six pregnant women (13-25 weeks of gestation) were divided in two groups - patients with symptoms of imminent spontaneous abortion and poor pregnancy outcome and patients with normal course of pregnancy. Double serum samples were analyzed to quantify IgM and IgG to parvovirus B19. RESULTS: Among pregnant women with symptoms of spontaneous abortion, we found significantly higher percentage of acute parvovirus B19 infection. CONCLUSIONS: Asymptomatic parvo B19 infection is associated with poor fetal outcome much more than we presumed previously.
Asunto(s)
Enfermedades del Recién Nacido/epidemiología , Infecciones por Parvoviridae/epidemiología , Parvovirus B19 Humano , Complicaciones Infecciosas del Embarazo/epidemiología , Resultado del Embarazo/epidemiología , Adolescente , Adulto , Femenino , Muerte Fetal/epidemiología , Muerte Fetal/etiología , Humanos , Recién Nacido , Transmisión Vertical de Enfermedad Infecciosa/estadística & datos numéricos , Infecciones por Parvoviridae/complicaciones , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/transmisión , Parvovirus B19 Humano/fisiología , Embarazo , Índice de Severidad de la Enfermedad , Adulto JovenRESUMEN
Common use of available techniques detecting perinatal infections needs to be accompanied with knowledge of proper interpretation of the tests and indications for treatment as well as communication with patients. The aim of this paper is to summarize current standards of diagnosis and treatment of infections in pregnant women and neonates. The detection of specific IgG antibodies in pre-conceptive period excludes the risk of transplacental Tg and PVB19 infection, while the risk of CMV infection is diminished and probable symptoms alleviated. Confirmed diagnosis of primary infection during pregnancy: 1. Toxoplasmosis (seroconversion, presence of IgA and IgM, low avidity IgG, PCR in amniotic fluid) is an indication for antimicrobial therapy; 2. Symptomatic CMV infection [seroconversion, virus detected in blood and urine (PCR, pp65 antigen)] for prophylactic IgG administration in mother; 3. PVB19 (seroconversion, IgM, PCR in blood and amniotic fluid) for frequent ultrasonographic evaluation of possible symptoms of fetal hydrops, and fetal transfusin if hydrops occurs. Diagnosis and treatment of the neonates should be managed in specialized c enters. Further monitoring of the infection is handicapped by the presence of maternal antibodies as well as the suppression of neonatal production of specific IgA and IgM. Toxoplasmosis requires from 6 (in asymptomatic infestation) to 12 months (in symptomatic infestation) treatment with pyrimethamine and sulfadiazine with supplementation of folinic acid. In symptomatic CMV infection 6 weeks treatment with ganciclovir is legitimate (decreases viruria and the risk of hearing impairment); while in asymptomatic infection with massive viral replication it can be considered as supposedly beneficial. The impact of prolonged treatment (over 6 weeks) as well as oral antiviral (valganciclovir) is currently under clinical investigation. The educational efforts should include: methods of preventing infections (Tg, CMV), necessity of repeated testing and treatment in pregnancy (Tg, PVB19), treatment of the neonate (Tg, CMV) and breastfeeding (CMV).
Asunto(s)
Infecciones por Citomegalovirus/congénito , Infecciones por Citomegalovirus/prevención & control , Transmisión Vertical de Enfermedad Infecciosa/prevención & control , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/prevención & control , Complicaciones Infecciosas del Embarazo/diagnóstico , Toxoplasmosis Congénita/diagnóstico , Toxoplasmosis Congénita/prevención & control , Adulto , Antivirales/uso terapéutico , Infecciones por Citomegalovirus/diagnóstico , Infecciones por Citomegalovirus/transmisión , Femenino , Humanos , Recién Nacido , Infecciones por Parvoviridae/diagnóstico , Infecciones por Parvoviridae/transmisión , Parvovirus B19 Humano/aislamiento & purificación , Embarazo , Complicaciones Infecciosas del Embarazo/prevención & controlRESUMEN
OBJECTIVE: We describe the clinical course of an infant who presented with severe fetal anemia and fetal hydrops following congenital parvovirus B19 infection before 16 gestational weeks. The fetus was treated by cordocentesis and intrauterine transfusion at 18 weeks. RESULTS: The infant demonstrated mild unilateral ventriculomegaly on antenatal magnetic resonance imaging, and polymicrogyria and heterotopia on postnatal magnetic resonance imaging. CONCLUSION: This adds to the evidence in recent literature of central nervous system damage associated with congenital parvovirus B19 infection.
Asunto(s)
Encefalopatías/virología , Encéfalo/anomalías , Coristoma/virología , Encefalitis Viral/complicaciones , Infecciones por Parvoviridae/complicaciones , Parvovirus B19 Humano , Adulto , Transfusión de Sangre Intrauterina , Encéfalo/virología , Encefalopatías/congénito , Encefalopatías/patología , Movimiento Celular , Coristoma/congénito , Coristoma/patología , Encefalitis Viral/congénito , Encefalitis Viral/patología , Femenino , Humanos , Hidropesía Fetal/terapia , Recién Nacido , Imagen por Resonancia Magnética , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/patología , Embarazo , Ultrasonografía PrenatalRESUMEN
We present a case of congenital parvovirus B19 infection in a term neonate manifested with isolated massive hydrothorax and mild anemia. Parvovirus B19 DNA was detected in maternal and neonatal blood as well as in pleural fluid despite lack of suggestive serology.
Asunto(s)
Hidrotórax/diagnóstico , Transmisión Vertical de Enfermedad Infecciosa , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/transmisión , Parvovirus B19 Humano/aislamiento & purificación , Complicaciones Infecciosas del Embarazo/virología , Adulto , Antibacterianos/uso terapéutico , Diagnóstico Diferencial , Drenaje/métodos , Femenino , Estudios de Seguimiento , Edad Gestacional , Humanos , Hidrotórax/congénito , Hidrotórax/terapia , Recién Nacido , Masculino , Infecciones por Parvoviridae/diagnóstico , Infecciones por Parvoviridae/terapia , Embarazo , Complicaciones Infecciosas del Embarazo/diagnóstico , Diagnóstico Prenatal , Síndrome de Dificultad Respiratoria del Recién Nacido/diagnóstico , Síndrome de Dificultad Respiratoria del Recién Nacido/terapia , Medición de Riesgo , Resultado del TratamientoRESUMEN
OBJECTIVE: In nonimmune pregnant woman, the primary infection with parvovirus B19 may lead to transplacental transmission to the fetus with variable outcomes, including congenital anemia, hydrops fetalis, fetal death or spontaneous resolution. CASE REPORT: The first case was of a 28-year-old woman, gravida 2, para 1, whose fetus was found to have left-sided pleural effusion on a sonogram at 29 weeks of gestation. A sample of aspirated pleural fluid was positive for parvovirus B19 by polymerase chain reaction. Cordocentesis showed fetal hemoglobin level of 5.0 g/dL. Intraperitoneal transfusion (IPT) was performed, because access to the fetal circulation was difficult. Thirty milliliters of group O, Rh-positive packed red cells were transfused into the peritoneal cavity. A non-hydropic baby weighing 2,680 g was delivered at 33 weeks of gestation. The neonates complete blood count examination showed a hemoglobin level of 16.3 g/dL. The newborn baby was discharged in stable condition. The second case was of a 31-year-old woman, gravida 2, para 1, whose fetus was found to have ascites, hypertrophic cardiomyopathy, and placentomegaly on a sonogram at 23 weeks of gestation. An amniotic fluid sample was positive for parvovirus B19 DNA by polymerase chain reaction. Fetal ascites and hypertrophic cardiomyopathy gradually resolved after maternal iron supplementation and 2 weeks of intrauterine digitalization therapy. A healthy infant weighing 3,198 g was delivered at 37 weeks of gestation. The neonates complete blood count examination showed a hemoglobin level of 10.3 g/dL. CONCLUSION: Termination of pregnancy is rarely indicated, because B19 virus is not teratogenic. Although intravascular transfusion offers obvious theoretical advantages, in some cases in which access to the fetal circulation is difficult or impossible, IPT should be performed combined with appropriate medical treatment. Thus, there is still a place for IPT in modern management of the severely anemic fetus, and this technique should not be neglected.
Asunto(s)
Transfusión de Sangre Intrauterina , Cardiotónicos/uso terapéutico , Digoxina/uso terapéutico , Transmisión Vertical de Enfermedad Infecciosa , Infecciones por Parvoviridae , Parvovirus B19 Humano/patogenicidad , Complicaciones Infecciosas del Embarazo , Ultrasonografía Prenatal , Adulto , Amniocentesis , Cordocentesis , Femenino , Humanos , Hidropesía Fetal , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/diagnóstico por imagen , Infecciones por Parvoviridae/terapia , Infecciones por Parvoviridae/transmisión , Derrame Pleural/terapia , Derrame Pleural/virología , Embarazo , Complicaciones Infecciosas del Embarazo/terapia , Complicaciones Infecciosas del Embarazo/virología , Segundo Trimestre del Embarazo , Nacimiento PrematuroRESUMEN
Parvovirus B19 is a small single-stranded DNA virus and a potent inhibitor of erythropoiesis, due to its cytotoxicity to erythroid progenitor cells. Infection with parvovirus B19 during pregnancy can cause several serious complications in the fetus, such as fetal anemia, neurological anomalies, hydrops fetalis, and fetal death. Early diagnosis and treatment of intrauterine parvovirus B19 infection is essential in preventing these fetal complications. Testing maternal serum for IgM antibodies against parvovirus B19 and DNA detection by PCR can confirm maternal infection. If maternal infection has occurred, ultrasound investigation of the fetus and measurement of the peak systolic flow velocity of the middle cerebral artery are sensitive non-invasive procedures to diagnose fetal anemia and hydrops. Intrauterine transfusion is currently the only effective treatment to alleviate fetal anemia, but if the fetus is (near) term, induction of delivery should be considered. Most maternal infections with parvovirus B19 occur through contact with infected children at home. Individual counseling of susceptible pregnant women will reduce unnecessary fetal deaths.
Asunto(s)
Enfermedades Fetales/diagnóstico , Infecciones por Parvoviridae/diagnóstico , Parvovirus B19 Humano , Complicaciones Infecciosas del Embarazo/diagnóstico , Anemia/congénito , Anemia/diagnóstico , Anemia/etiología , Transfusión de Sangre Intrauterina , Femenino , Enfermedades Fetales/diagnóstico por imagen , Humanos , Recién Nacido , Transmisión Vertical de Enfermedad Infecciosa , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/diagnóstico por imagen , Infecciones por Parvoviridae/terapia , Infecciones por Parvoviridae/transmisión , Embarazo , Complicaciones Infecciosas del Embarazo/diagnóstico por imagen , UltrasonografíaRESUMEN
Leukoerythroblastosis is a rarely observed disease characterized by the presence of leukocytosis, erythroid and myeloid blast cells in peripheral blood. To our knowledge, it had not been diagnosed in a premature newborn before the case we report have.A female baby weighing 1164 grams, who was born prematurely at the 29th week of gestation by Cesarean section was referred to our newborn intensive care unit due to prematurity and respiratory distress with no prenatal pathological findings. Physical examination revealed tachypnea and hepatosplenomegaly. Routine laboratory measurements showed significant leukocytosis (85,000/mm3) and anemia (Hb: 9.6 g/dL and Hct: 27.6%). The platelet count was normal. The peripheral blood smear suggested leukoerythroblastosis with the presence of nucleated erythrocytes, monocytosis, and 4% blasts. Bone marrow cytogenetic examination was normal. Parvovirus B19 Ig G and M serology were detected to be positive. The etiological factors observed in leukoerythroblastosis occurring during neonatal and early childhood period are congenital-postnatal viral infections, juvenile myelomonocytic leukemia and osteopetrosis. To our knowledge, no case of leukoerythroblastosis in such an early phase has been reported in the in literature. As a result, premature delivery and leukoerythroblastosis were thought to have developed secondary to intrauterine parvovirus B19 infection. Leukoerythroblastosis is a rarely observed disease characterized by the presence of leukocytosis, erythroid and myeloid blast cells in peripheral blood. It is reported that it can be observed following hematologic malignancies especially juvenile myelomonocytic leukemia, acute infections, hemolytic anemia, osteopetrosis, myelofibrosis, neuroblastoma and taking certain medicines. To our knowledge, it has not been diagnosed in a premature newborn before. Here we the case of a newborn who was referred to our intensive care unit due to being born prematurely at the 29th week of gestation and diagnosed with leukoerythroblastosis.
Asunto(s)
Anemia Mielopática/congénito , Enfermedades del Prematuro/virología , Infecciones por Parvoviridae/congénito , Parvovirus B19 Humano/aislamiento & purificación , Adulto , Anemia Mielopática/terapia , Anemia Mielopática/virología , Anticuerpos Antivirales/sangre , Transfusión Sanguínea , Femenino , Enfermedades Fetales/virología , Edad Gestacional , Humanos , Inmunoglobulina G/sangre , Inmunoglobulina M/sangre , Recién Nacido , Recien Nacido Prematuro , Parvovirus B19 Humano/inmunología , EmbarazoRESUMEN
OBJECTIVE: To analyse 3 cases of parvovirus B19 infection in a pregnant woman followed by transplacental transmission to the fetus. DESIGN: A reprospective study. SETTING: Department of Obstetrics and Gynecology, University Hospital, Olomouc. METHOD: Parvovirus B19 vertical transmission from a pregnant woman to the fetus was diagnosed in 3 cases. Serologic testing of IgG and IgM antibodies against parvovirus B19, cytological bone marrow examination and parvovirus B19 DNA analysis by PCR methods were performed. The fetal anemia was predicted by measurements of peak systolic velocities in the middle cerebral artery (MCA-PSV). RESULTS: There were three pregnancies in all (1st - single, 2nd and 3rd - dizygotic twins). In the 1st and 2nd pregnancy the diagnosis of parvovirus B19 infection was set on the basis of erythroblastopenia diagnosed in the neonatal period or early infancy. In the 2nd pregnancy (dizygotic twins) intrauterine death of one twin occured. In the 3rd case (dizygotic twins) the diagnosis was already set in the 20th week of pregnancy. Subsequently the fetal anemia was predicted by doppler examination. The fetuses did not require invasive intrauterine intervention and mild anemia was diagnosed after delivery. Progressive intrauterine growth retardation of one twin was observed. Neither cardiomegaly nor fetal hydrops did not occur. All mothers were asymptomatic during the whole pregnancy. CONCLUSION: Parvovirus B19 infection should be excluded in all cases of nonimmune fetal hydrops, severe fetal anemia, cardiomegaly, intrauterine growth retardation (IUGR) and chronic erythroblastopenia diagnosed in the neonatal period or early infancy. The presence of IgM and IgG antibodies against parvovirus B19 is highly specific but their negativity is insufficient for the exclusion of a parvovirus B19 infection. Viral DNA testing by PCR method is the only reliable method available.
Asunto(s)
Enfermedades en Gemelos , Enfermedades Fetales/diagnóstico , Transmisión Vertical de Enfermedad Infecciosa , Infecciones por Parvoviridae/diagnóstico , Parvovirus B19 Humano , Complicaciones Infecciosas del Embarazo/diagnóstico , Adulto , Anemia/congénito , Anemia/etiología , Femenino , Humanos , Recién Nacido , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/transmisión , EmbarazoRESUMEN
OBJECTIVE: In some cases of non-immune hydrops there is congenital or acquired fetal anemia. The aim of this study was to investigate the potential value of fetal middle cerebral artery peak systolic velocity (MCA-PSV) in the assessment and management of non-immune hydrops due to anemia. METHODS: Fetal MCA-PSV and fetal hemoglobin concentration, in blood obtained by cordocentesis, were measured in 16 singleton pregnancies referred to our unit for further investigations because of a diagnosis of non-immune hydrops fetalis. In all cases a detailed ultrasound examination demonstrated moderate or severe ascites, with or without skin edema, and pericardial or pleural effusions. Furthermore, there were no obvious malformations to account for the hydrops. In each fetus the measured MCA-PSV and hemoglobin concentration were expressed as delta values (the difference in SD from the normal mean for gestation). Regression analysis was used to determine the significance of the association between delta MCA-PSV and delta fetal hemoglobin concentration. In addition, we searched our database to identify the sonographic features and hemoglobin concentration of fetuses with congenital infection. RESULTS: In the 16 cases of non-immune hydrops there were seven with parvovirus B19 infection, one each of alpha-thalassemia and primary cardiomyopathy and seven with no obvious explanation for the hydrops. There was a significant association between delta MCA-PSV and delta hemoglobin concentration (delta hemoglobin = (delta MCA-PSV + 0.1437)/-0.4154; R(2) = 0.7202; P < 0.0001). In 10 of the cases the fetal hemoglobin concentration was more than 4 SD below the normal mean for gestation and in all these cases the MCA-PSV was more than 2 SD above the normal mean for gestation. Our computer search identified an additional nine fetuses with parvovirus B19 infection and in all cases the predominant sonographic finding was ascites and the hemoglobin concentration was more than 4 SD below the normal mean. In contrast, only 3/14 fetuses with cytomegalovirus, toxoplasmosis, coxsackie B or Treponema infection had ascites and only 2/14 had a hemoglobin deficit of 4-6 SD. CONCLUSION: In the management of non-immune hydrops, measurement of fetal MCA-PSV can help identify the subgroup with fetal anemia.
Asunto(s)
Hidropesía Fetal/diagnóstico por imagen , Arteria Cerebral Media/diagnóstico por imagen , Anemia/sangre , Anemia/diagnóstico por imagen , Velocidad del Flujo Sanguíneo , Estudios Transversales , Femenino , Sangre Fetal/química , Enfermedades Fetales/sangre , Enfermedades Fetales/diagnóstico por imagen , Hemoglobinas/análisis , Humanos , Hidropesía Fetal/virología , Arteria Cerebral Media/embriología , Arteria Cerebral Media/fisiología , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/diagnóstico por imagen , Embarazo , Análisis de Regresión , Sístole , UltrasonografíaRESUMEN
In the 24th week of gestation we diagnosed a severe hydrops fetalis in a 25 year old VI gravid III para, who had contact to parvovirus B19 in the 14th week of gestation. Because of the severe anaemia of the fetus and the massively increased bilirubinoides in the amniotic fluid we decided at the same day to apply the first of four intrauterine transfusions. The serological patterns of maternal blood with highly positive parvovirus-B19-IgG and negative IgM suggested that an infection had occurred. Parvoviral DNA was found in maternal and fetal blood confirming the diagnosis of an acute intrauterine parvovirus-B19 infection. No viral DNA was detected in fetal ascites. IgM in fetal blood was negative. By means of four transfusions, the pregnancy could be prolonged until the 32 + 5th week of gestation while the ascites was declining. When rupture of membranes occurred, a cesarean section had to be performed due to contractions and presentation of the feet. The newborn's blood count exhibited a thrombocytopenia with normal haemoglobin and haematocrit. Five days after delivery, a blood exchange had to be done because of a hyperbilirubinaemia. After seven weeks, the child could be dismissed from hospital in good general status, with decreasing ascites, normal liver function and normal neurological status. The blood of the newborn was tested to be positive for IgG, while IgM-antibodies and parvovirus-B19-DNA were negative. The diagnosis of a parvovirus-B19 infection of a fetus with severe hydrops and anaemia could be verified by a positive proof for DNA in maternal blood, with negative IgM and highly positive parvovirus-B19-IgG and on the other hand highly positive viral DNA in fetal blood and in the amniotic fluid. 10 weeks after contact to parvovirus B19, i. e. in the 24th week of gestation, positive IgG- and negative IgM-antibodies were found in the mother's blood, whereas fetal complications were noticed. These data demonstrate that following an acute parvovirus-B19-infection of the mother IgM-antibodies can be proofed for 6 - 8 (- 10) weeks. On the other side parvovirus-B19-DNA in the mothers blood is detectable by means of PCR for 8 - 10 weeks and in some cases even more than 15 weeks.
Asunto(s)
Enfermedades Fetales/diagnóstico , Transmisión Vertical de Enfermedad Infecciosa , Infecciones por Parvoviridae/congénito , Parvovirus B19 Humano , Complicaciones Infecciosas del Embarazo/diagnóstico , Adulto , Transfusión de Sangre Intrauterina , ADN Viral/sangre , Femenino , Enfermedades Fetales/terapia , Humanos , Hidropesía Fetal/diagnóstico , Hidropesía Fetal/terapia , Inmunoglobulina G/sangre , Inmunoglobulina M/sangre , Recién Nacido , Infecciones por Parvoviridae/diagnóstico , Infecciones por Parvoviridae/terapia , Infecciones por Parvoviridae/transmisión , Parvovirus B19 Humano/genética , Embarazo , Complicaciones Infecciosas del Embarazo/virología , Segundo Trimestre del EmbarazoRESUMEN
Parvovirus B19 is a common, self-limiting, usually benign childhood virus that causes erythema infectiosum, also known as fifth disease. Acute infection in pregnancy can cause B19 infection in the fetus, leading to nonimmune fetal hydrops or fetal loss, depending on gestational age at the time of infection. Susceptibility to parvovirus B19 infection should be determined in selected pregnant women at high risk for exposure, and counseling should be provided regarding prevention, testing, and treatment options if exposed.
Asunto(s)
Transmisión Vertical de Enfermedad Infecciosa/prevención & control , Infecciones por Parvoviridae/enfermería , Complicaciones Infecciosas del Embarazo/enfermería , Eritema Infeccioso/prevención & control , Femenino , Humanos , Recién Nacido , Enfermería Maternoinfantil , Infecciones por Parvoviridae/congénito , Infecciones por Parvoviridae/transmisión , Parvovirus B19 Humano , Embarazo , Complicaciones Infecciosas del Embarazo/prevención & controlRESUMEN
Human parvovirus B19 causes the fifth disease (erythema infectiosum) in childhood. Intrauterine infection by parvovirus in immunocompromised fetus can lead to the severe congenital aplastic anemia. Here we report the case of 2.5-year-old girl with congenital infection with parvovirus B19. The girl was born as a pre-term baby with hydrops, congenital aplastic anemia, and low level of immunoglobulins IgG and IgM. She depended on the repeated blood transfusions and she did not respond to erythropoietin therapy. The parvovirus B19 infection in bone marrow was detected by polymerase chain reaction and its therapy started with intravenous administration of immunoglobulins. Hemoglobin reached normal level one year later, but low levels of parvovirus B19 were detectable for another 6 months. Immunoglobulin treatment was finished when the virus could not be detected in the circulation. However, one-month later parvovirus B19 DNA was detected again. The two months course of immunoglobulin treatment was repeated, and the DNA analysis of blood cells for parvovirus B19 has been negative since then. Five months after the final withdrawal of the immunoglobulin therapy the girl is in a good shape and all lab tests, except for the decreased levels of IgM, are within the normal range. The PCR monitoring of the presence of parvovirus B19 DNA in blood and bone marrow cells during and after the treatment of congenital aplastic anemia caused by parvovirus B19 chronic infection becomes the necessity for the rational therapy.