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1.
Minerva Pediatr ; 55(3): 283-6, 286-8, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12900714

ABSTRACT

The authors describe the case of a 1-month-old patient admitted for crisis of paleness, accompanied by hyporeactivity, tachycardia and polypnea; the symptoms, attenuated after detension of the abdomen, grew worse, with compromise of general conditions and respiratory failure. Chest X-ray shows the herniation of intestinal loops in the thoracic cavity. After the first emergency care, it became necessary to submit the baby to HFO and cardiovascular drugs for some hours before getting oxygenation index (OI) and circulation stabilization. Late presenting congenital diaphragmatic hernia (LCDH) is a condition that can occur during first or second infancy with respiratory or abdominal symptoms, quickly worsening or intermittent. The prognosis is good if diagnosis is timely. Patient stabilization before surgical intervention must be valued not only by O.I. but also by circulation conditions.


Subject(s)
Hernia, Diaphragmatic/diagnosis , Hernias, Diaphragmatic, Congenital , Age Factors , Humans , Infant , Male
2.
J Pediatr Surg ; 36(6): 944-5, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11381433

ABSTRACT

The authors report the first neonatal presentation of a congenital giant megaureter (CGM), a very rare unilateral urinary anomaly, which is defined as "a ureter whose lumen is congenitally, focally and segmentally dilated to more than 10 times the normal diameter, in presence of normal bladder volume and function." The definition of CGM is purely descriptive; it can be secondary to several different diseases, and in the series of 21 CGM (12 in duplex system) reported by Chen-Ju Huang, the morphology of the distal ureter varied from a near normal caliber to a ureteral stenosis, a ureterocele or a complete ureteral atresia. J Pediatr Surg 36:944-945.


Subject(s)
Ureter/abnormalities , Abnormalities, Multiple , Dilatation, Pathologic , Humans , Infant, Newborn , Kidney/abnormalities , Male , Urogenital Abnormalities/pathology , Urogenital Abnormalities/surgery
3.
Ann Thorac Surg ; 69(1): 267-9, 2000 Jan.
Article in English | MEDLINE | ID: mdl-10654531

ABSTRACT

The sternal cleft is a rare congenital anomaly resulting from a fusion failure of the sternum, generally observed at birth and asymptomatic. Surgery is indicated to protect the heart and major vessels from trauma, to improve respiratory dynamics, and for aesthetic reasons. We observed 2 neonates for a superior and medial thoracic mass. The defect involved the upper two thirds of the sternum. The surgical operation for both patients consisted in the primary closure of the defect.


Subject(s)
Sternum/abnormalities , Aorta/anatomy & histology , Clavicle/abnormalities , Esthetics , Follow-Up Studies , Heart/anatomy & histology , Humans , Infant, Newborn , Male , Manubrium/abnormalities , Neck Muscles/surgery , Pectoralis Muscles/surgery , Respiration , Sternum/surgery , Suture Techniques
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