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1.
J Coll Physicians Surg Pak ; 31(3): 346-349, 2021 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-33775031

RESUMEN

Pulmonary artery sling is an uncommon entity in the neonatal period. It is defined as an abnormally originated left pulmonary artery arising from the posterior aspect of right pulmonary artery. Because of the associated structures in this region, mostly originating from sixth aortic arch, tracheobronchial anomalies and congenital heart defects, it frequently accompanies the pulmonary artery sling. Etiology of pulmonary artery sling has not been determined to date. Surgical correction is necessary even for asymptomatic cases because of the high mortality. Postoperative mortality is commonly associated with airway defects. Therefore, prompt diagnosis and timely intervention decrease the morbidity and mortality. We, herein, present a case of a neonate with isolated pulmonary artery sling un-associated with their developmental anomalies. Antenatal history was positive for maternal hypothyroidism, for which she was taking L-thyroxine. To the best of our knowledge, this is the first pulmonary artery sling case accompanied by maternal hypothyroidism. Key Words: Pulmonary artery sling, Neonate, Hypothyroidism.


Asunto(s)
Cardiopatías Congénitas , Estenosis Traqueal , Malformaciones Vasculares , Femenino , Humanos , Recién Nacido , Pulmón , Embarazo , Arteria Pulmonar/diagnóstico por imagen , Arteria Pulmonar/cirugía
2.
Turk J Pediatr ; 60(3): 306-309, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30511544

RESUMEN

Yilmaz-Semerci S, Bornaun H, Kurnaz D, Cebeci B, Babayigit A, Büyükkale G, Çetinkaya M. Neonatal atrial flutter: Three cases and review of the literature. Turk J Pediatr 2018; 60: 306-309. Atrial flutter (AFl) is known to be a seldom type of fetal and neonatal arrhythmia. Although it could end in severe morbidities such as hydrops fetalis or even death, with early prenatal diagnosis and prompt therapeutic approaches the majority of AFl cases show good prognosis. Neonatal AFl might be resistant to first step therapies. Therefore, secondary agents like flecainide, amiodarone, sotalol and cardioversion, if required, could be influent in perinatal tachyarrhythmia. In addition, close follow-up even after discharge is very important to keep all follow-up appointments. Herein, we present three cases of fetal/neonatal AFl in light of the literature and discuss the characteristics, diagnosis and treatment options.


Asunto(s)
Antiarrítmicos/uso terapéutico , Aleteo Atrial/diagnóstico , Cardioversión Eléctrica/métodos , Aleteo Atrial/terapia , Electrocardiografía , Femenino , Humanos , Recién Nacido , Masculino , Embarazo , Ultrasonografía Prenatal/métodos
3.
J Pediatr Pharmacol Ther ; 23(3): 219-222, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29970979

RESUMEN

Pulmonary atelectasis leads to difficulties in weaning of the neonates from mechanical ventilation. The management of persistent atelectasis in neonates constitutes a common challenge for physicians. Several reports suggested Recombinant human DNase (rhDNase) as a beneficial therapy for neonates with persistent atelectasis by reducing mucous viscosity. No adverse effect associated with rhDNase treatment was reported in neonates. Herein, we report probable adverse reactions associated with rhDNase use in a preterm infant. Therefore, we suggest that clinicians must be aware of this reaction in neonates and should carefully follow up these infants for the development of adverse reactions. We think that more clinical experience and data are needed to define its tolerability and adverse effect profile in neonates.

4.
Turk J Pediatr ; 60(6): 751-754, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-31365216

RESUMEN

Yilmaz-Semerci S, Güzelbey T, Kurnaz D, Kalkan S, Çetinkaya M. A rare case of cephalothoracopagus janiceps conjoined twins. Turk J Pediatr 2018; 60: 751-754. Conjoined twins represent a rare phenomenon of a monochorionic monoamniotic twin. Five types of conjoined twins have been described and thoracocephalopagus was reported to be seen with an incidence of 1 in 3 million. The etiology has not been elucidated yet. Therefore, more data is required to understand this entity better. Herein, we report a case of thoracocephalopagus.

5.
J Coll Physicians Surg Pak ; 27(3): S38-S40, 2017 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-28302241

RESUMEN

Intestinal perforation or inflammation due to appendicitis is rarely encountered in the neonatal period. The diagnosis may be delayed due to the lack of specific clinical symptoms and its rarity in this patient population. Early surgical treatment is the main treatment strategy with a good prognosis. However, delayed diagnosis may result in complications and even death. Herein, we describe a late preterm female neonate without any risk factors who had a diagnosis of perforated appendicitis at postnatal day 5. To the authors' knowledge, this case represents the earliest presentation of neonatal perforated appendicitis elucidated by prompt diagnostic laparotomy. Neonatal appendicitis should be considered in the differential diagnosis of infants with abdominal clinical findings.


Asunto(s)
Apendicitis/complicaciones , Apendicitis/diagnóstico , Enfermedades del Prematuro/diagnóstico , Enfermedades del Prematuro/etiología , Perforación Intestinal/etiología , Apendicitis/cirugía , Femenino , Humanos , Recién Nacido , Recien Nacido Prematuro , Enfermedades del Prematuro/cirugía , Perforación Intestinal/diagnóstico , Perforación Intestinal/cirugía
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