keyword
https://read.qxmd.com/read/34645629/severe-fetal-anaemia-caused-by-congenital-cytomegalovirus-infection
#41
JOURNAL ARTICLE
Claudia Salazar-Sanchez, Pedro Llancarí, Rommy H Novoa, Walter Ventura
A 22-year-old pregnant woman was referred to our fetal medicine unit due to severe fetal growth restriction at 26 weeks of gestation. An extensive detailed ultrasound revealed signs of bilateral periventricular hyperechogenicity, suggesting fetal infection potentially due to cytomegalovirus (CMV). Doppler ultrasound showed a high peak systolic velocity in the middle cerebral artery. Percutaneous umbilical cord blood sampling confirmed fetal CMV infection and severe fetal anaemia. We present this case to highlight the importance of fetal anaemia, which can be fatal regardless of whether it is associated with generalised oedema or hydrops fetalis...
October 13, 2021: BMJ Case Reports
https://read.qxmd.com/read/34404669/management-of-hyponatraemia-in-pre-eclampsia-with-severe-features
#42
JOURNAL ARTICLE
Julia Whitley, Sarah Swartz, Anjali Martinez
Pre-eclampsia is a common pregnancy complication with many associated maternal and fetal risks, yet its pathophysiology remains poorly understood. Hyponatraemia is a rarely described finding in pre-eclampsia that has been associated with both maternal and fetal complications and medically indicated delivery. We present a case of hyponatraemia in a patient admitted for induction of labour for gestational hypertension, which developed into pre-eclampsia with severe features requiring magnesium sulfate therapy for seizure prophylaxis...
August 17, 2021: BMJ Case Reports
https://read.qxmd.com/read/34400420/neonatal-dengue-an-under-diagnosed-entity
#43
JOURNAL ARTICLE
Bharti Yadav, Neeraj Gupta, Ravisekhar Gadepalli, Vijaya Lakshmi Nag
Neonatal dengue is an under-diagnosed disease likely due to low index of suspicion along with its resemblance to sepsis. We hereby report two cases of neonatal dengue, highlighting the need of high degree of suspicion in infants born to febrile mothers even with maternal serology being negative. Moreover, severity of neonatal illness positively correlates with the maternal disease.
August 16, 2021: BMJ Case Reports
https://read.qxmd.com/read/34381528/-sars-cov-2-infection-in-pregnant-women-epidemiological-clinical-biological-and-evolutionary-profile-in-16-cases-the-covid-19-experience-in-the-moroccan-military-hospital-in-benslimane
#44
Abdelhamid Benlghazi, Saad Benali, Yassine Bouhtouri, Moad Belouad, Hamza Massoudi, Jaouad Kouach
The first cases of infection caused by new SARS-CoV-2 coronavirus were reported in China in December 2019. This disease is called COVID-19 and has been declared as a pandemic by the WHO three months after its outbreak (in March 2020). In most cases it results in non-severe infectious syndrome associated with different degrees of benign symptoms (fever, cough, myalgia, headache and potential digestive disorders). SARS-CoV-2 can cause severe lung diseased and, sometimes, it results in death. Data on its consequences during pregnancy are limited...
2021: Pan African Medical Journal
https://read.qxmd.com/read/34380672/multidisciplinary-management-of-pregnancy-and-labour-in-a-patient-with-glycogen-storage-disease-type-1a
#45
JOURNAL ARTICLE
Alice May Jones, Clare Tower, Diane Green, Karolina M Stepien
Glycogen storage disease type 1a (GSD 1a) is a metabolic disorder caused by deficiency of an enzyme required for glycogen breakdown, causing hypoglycaemia and lactic acidosis. Metabolic derangements cause disease manifestations affecting the kidneys, liver and platelet function. Physiological changes in pregnancy worsen fasting intolerance and increase reliance on exogenous glucose to avoid lactic acidosis. Fetal macrosomia and declining respiratory function result in high rates of caesarean sections. We report the multidisciplinary team (MDT) management of a 25-year-old woman with GSD 1a in an unplanned pregnancy...
August 11, 2021: BMJ Case Reports
https://read.qxmd.com/read/34344663/congenital-focal-eventration-of-the-left-hemidiaphragm-diagnostic-dilemma-resolved-on-prenatal-mri
#46
JOURNAL ARTICLE
Anubhuti Rana, Smita Manchanda, Vatsla Dadhwal
No abstract text is available yet for this article.
August 3, 2021: BMJ Case Reports
https://read.qxmd.com/read/34326114/when-diamniotic-twins-suddenly-become-monoamniotic-twins-spontaneous-septostomy-of-the-dividing-membrane
#47
JOURNAL ARTICLE
Angela Vidal, Cristina Nastasia, Markus Hodel, Joachim Kohl
In twin pregnancies, amnionicity and chorionicity are crucial as they strongly determine prenatal and perinatal management. First trimester ultrasound allows a highly reliable diagnosis of amnionicity and chorionicity, making it an internationally accepted standard in antenatal care. However, in rare cases, amnionicity can change from diamniotic to monoamniotic throughout pregnancy, substantially impacting perinatal management. We report the case of a confirmed monochorionic diamniotic twin pregnancy with a diagnosis of spontaneous septostomy of the dividing membrane (SSDM) at 28 weeks of gestation, resulting in a pseudomonoamniotic pregnancy...
July 29, 2021: BMJ Case Reports
https://read.qxmd.com/read/34290017/neonatal-polycystic-kidney-disease-a-novel-variant
#48
JOURNAL ARTICLE
Catherine Finnegan, Claire Murphy, Fionnuala Breathnach
Polycystic kidney disease (PKD) is a condition typified by multiple renal cysts and renal enlargement. Classification is usually determined by mode of inheritance-autosomal dominant PKD (ADPKD) or autosomal recessive PKD (ARPKD). ARPKD frequently presents in fetal life, but here we report a rare case of a family with two siblings diagnosed with ADPKD manifesting in utero with novel genetic findings. During the first pregnancy, enlarged cystic kidneys were noted at the gestational age (GA) of 18 weeks, which became progressively larger and anyhdramnios ensued by GA of 25 weeks...
July 21, 2021: BMJ Case Reports
https://read.qxmd.com/read/34257134/pseudoamniotic-band-syndrome-after-bipolar-cord-coagulation-in-monochorionic-twins-complicated-by-twin-to-twin-transfusion-syndrome
#49
JOURNAL ARTICLE
Anubhuti Rana, Vatsla Dadhwal, Peyyala Shainy, K Aparna Sharma
No abstract text is available yet for this article.
July 13, 2021: BMJ Case Reports
https://read.qxmd.com/read/34253534/neonatal-presentation-of-phace-syndrome
#50
JOURNAL ARTICLE
James Williams, Terry Cullen, Karen L Atkin, Ruth K Armstrong
No abstract text is available yet for this article.
July 12, 2021: BMJ Case Reports
https://read.qxmd.com/read/34253517/congenital-cytomegalovirus-infection-in-twin-pregnancy
#51
JOURNAL ARTICLE
Ana Araújo Carvalho, Cláudia B Silva, Maria Luísa Martins, Gonçalo Cassiano Santos
Cytomegalovirus (CMV) infection is one of the preeminent congenital viral infections, and despite its potential morbidity, uncertainty about its physiopathology, prevention and treatment remains until now. We report a case of a dichorionic and diamniotic twin pregnancy in which only one of the fetus had signs of being affected. The first twin had prenatal diagnosis of intrauterine growth restriction and hyperechogenic bowel, attributable to CMV infection, while there was no evidence of infection of the second one...
July 12, 2021: BMJ Case Reports
https://read.qxmd.com/read/34244192/accurate-prenatal-discrimination-of-placenta-accreta-spectrum-from-uterine-dehiscence-is-necessary-to-ensure-optimal-management
#52
JOURNAL ARTICLE
Theophilus Kofi Adu-Bredu, Atta Owusu-Bempah, Sally Collins
Uterine scar dehiscence with underlying placenta is often misdiagnosed as placenta accreta spectrum both prenatally and intraoperatively due to the absence of myometrial tissue in the area. Misdiagnosis generates obstetric anxiety and results in overtreatment which carries a risk of iatrogenic injury. We present a case of the antenatal diagnosis of uterine dehiscence in a 36-year-old woman with a history of two caesarean deliveries and a low-lying placenta. We further describe the sonographic features useful for differentiating this condition from placenta accreta spectrum in instances where the placenta lies under an area of full thickness uterine scar dehiscence...
July 9, 2021: BMJ Case Reports
https://read.qxmd.com/read/34209533/can-sars-cov-2-induce-uterine-vascular-anomalies-and-poor-contractile-response-a-case-report
#53
Anca Lesnic, Bashar Haj Hamoud, Mircea-Octavian Poenaru, Valentin-Tiberiu Moldovan, Radu Chicea, Romina-Marina Sima, Mihai Popescu, Liana Ples
We are reporting a case of a 36 year-old Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) positive hypertensive primigravida with postpartum uterine atony that required emergency subtotal hysterectomy at Saint John Hospital Bucur Maternity Bucharest. The maternity was designated as the Coronavirus Disease 2019 (COVID-19) Maternity for Bucharest and Ilfov County since March 2020. The patient was mildly symptomatic for SARS-CoV-2, infection confirmed with reverse transcription polymerase chain reaction (RT-PCR)...
June 29, 2021: Medicina
https://read.qxmd.com/read/34167992/premature-closure-of-ductus-arteriosus-after-a-single-dose-of-diclofenac-during-pregnancy
#54
JOURNAL ARTICLE
Constança Soares Dos Santos, Patricia Vaz Silva, Rui Castelo, Joaquim Tiago
A male term neonate was admitted to the neonatal intensive care unit in the first hours of life with central cyanosis. Echocardiogram showed severe biventricular hypertrophy, markedly right-sided, tricuspid regurgitation, a patent foramen ovale and a closed ductus arteriosus (CDA). The mother recalled being treated with a single dose of intravenous diclofenac for low back pain 2 weeks earlier. The newborn was started on propranolol with symptomatic improvement and was discharged on day 10. At 1-month follow-up, he showed complete resolution of ventricular hypertrophy and suspended propranolol...
June 24, 2021: BMJ Case Reports
https://read.qxmd.com/read/34011666/valsartan-exposure-in-pregnancy-with-resultant-anhydramnios-and-chronic-kidney-disease-in-a-late-preterm-infant
#55
JOURNAL ARTICLE
Sarah Petch, Emily O'Connor, Ailbhe McGrath, Sean Daly
In utero exposure to angiotensin II receptor blockers (ARBs) has fetotoxic effects including renal failure, oligohydramnios and lung hypoplasia. We present the case of a 24-year-old woman who presented to the maternity services in the 34th week of her first pregnancy. She was taking valsartan for hypertension. Ultrasound showed a structurally normal fetus with anhydramnios. The patient was admitted and valsartan was discontinued. She had spontaneous preterm delivery at 35 weeks' gestation of a baby girl. The baby's urine output was minimal in the first week of life and she was transferred to a paediatric hospital for specialist nephrology input...
May 19, 2021: BMJ Case Reports
https://read.qxmd.com/read/34011647/infant-presenting-with-pyloric-stenosis-and-autosomal-recessive-polycystic-kidney-disease-at-36-weeks-postmenstrual-age-pma
#56
JOURNAL ARTICLE
Tatiana A Nuzum, I Thomas Cohen, Christina Ferrucci-Da Silva, Erin Qualter
This case report describes a premature male infant born after a pregnancy complicated by oligohydramnios of unknown aetiology but otherwise unremarkable prenatal scans. He had sudden onset of projectile emesis and severe hypertension in the third week of life, and further investigations revealed both pyloric stenosis and polycystic kidneys, at just 36 weeks' postmenstrual age (PMA). His course thereafter was complicated by severe refractory hypertension requiring multiple antihypertensive agents in order to gain control, although his renal function remained normal...
May 19, 2021: BMJ Case Reports
https://read.qxmd.com/read/33989487/-not-available
#57
REVIEW
Lea Aurora Cupul-Uicab, José Ángel Hernández-Mariano, Argelia Vázquez-Salas, Ahidée Leyva-Lopez, Tonatiuh Barrientos-Gutierrez, Aremis Villalobos Hernández
Objetivo. Resumir la evidencia científica sobre efectos maternos y neonatales del Covid-19 durante el embarazo. Material y métodos. Se realizó una revisión rápida Cochrane y un metaanálisis de proporciones y razones de momios (RM). Resultados. Los eventos maternos más comunes fueron la ventilación mecánica invasiva y admisión a la unidad de cuidados intensivos (UCI); las complicaciones del embarazo fueron el sufrimiento fetal y la ruptura prematura de membranas; las comorbilidades fueron la obesidad y el asma...
February 26, 2021: Salud Pública de México
https://read.qxmd.com/read/33879461/tale-of-two-viruses-parvovirus-b19-and-hiv
#58
REVIEW
Hayley Hernstadt, Paul Randell, Sarah Fidler, Caroline Foster
We present a HIV-infected patient who developed severe anaemia due to chronic parvovirus B19 infection and subsequently had an unplanned pregnancy. This is in the context of poor adherence to antiretroviral therapy and significant immunosuppression; there was a delay in diagnosis of chronic parvovirus infection due to attribution of anaemia to HIV. She received immunoglobulin therapy and effective antiretroviral therapy, with reduction in parvovirus load and improvement in anaemia. She was counselled regarding the need for monitoring in pregnancy due to risk of intrauterine infection...
April 20, 2021: BMJ Case Reports
https://read.qxmd.com/read/33863770/non-immune-hydrops-fetalis-secondary-to-congenital-chylothorax-with-diffuse-interstitial-lung-disease-a-diagnostic-conundrum
#59
Alvin Jia Hao Ngeow, Mei Yoke Chan, Oon Hoe Teoh, Sarat Kumar Sanamandra, Daisy Kwai Lin Chan
A Chinese male infant was born at 35 weeks weighing 2935 g to a mother with polyhydramnios and prenatal hydrops fetalis. He developed marked respiratory distress secondary to bilateral congenital chylothorax and required pleural drainage, high frequency oscillation and inhaled nitric oxide therapy. He was extubated to non-invasive ventilation by day 14. There was no bacterial or intrauterine infection, haematologic, chromosomal or cardiac disorder. He was exclusively fed medium-chain triglyceride formula. High-resolution CT showed diffuse interstitial lung disease...
April 16, 2021: BMJ Case Reports
https://read.qxmd.com/read/33849878/chronic-histiocytic-intervillositis-chi-an-under-recognised-condition-with-potential-serious-sequelae-in-pregnancy
#60
JOURNAL ARTICLE
Ai Xin Lee, Brian Run Yi Tan, Chye Lee Kho, Kim Teng Tan
Chronic histiocytic intervillositis (CHI) is a rare placental disorder associated with adverse pregnancy outcomes and high recurrence rates in subsequent pregnancies. We discuss a case of CHI diagnosed incidentally in a young primigravida who presented with a first trimester miscarriage. CHI is usually diagnosed after an adverse pregnancy outcome by microscopic placental histopathology. Currently, CHI is a poorly understood condition by clinicians in many aspects, including its aetiology and subsequent management of patients in their future pregnancies...
April 13, 2021: BMJ Case Reports
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