1974
DOI: 10.1007/bf01314944
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Pulmonary varix diagnosed in a newborn

Abstract: Abstract. A case of a pulmonary varicose vein is described.A coin lesion was observed and persisted after a pneumonia during the first month of life. An anomalous pulmonary vessel was suspected by tomography, and was verified by selective pulmonary angiography when the infant was three months old.

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Cited by 5 publications
(3 citation statements)
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“…In contrast to the scimitar syndrome, no left‐to‐right shunt is produced. Various other terms have been used in the literature to describe what is essentially the same anomaly, including meandering pulmonary vein, 17–19 scimitar variant, 20–22 pseudo‐scimitar syndrome 23 and pulmonary varix 24–27 . While it has been suggested that these cases can be considered related congenital anomalies, few papers to date have acknowledged the full range of cases published under these varied names 19 .…”
Section: Discussionmentioning
confidence: 99%
“…In contrast to the scimitar syndrome, no left‐to‐right shunt is produced. Various other terms have been used in the literature to describe what is essentially the same anomaly, including meandering pulmonary vein, 17–19 scimitar variant, 20–22 pseudo‐scimitar syndrome 23 and pulmonary varix 24–27 . While it has been suggested that these cases can be considered related congenital anomalies, few papers to date have acknowledged the full range of cases published under these varied names 19 .…”
Section: Discussionmentioning
confidence: 99%
“…The malformation is most often latent, and discovered in the adult on a chest radiograph, practiced either fortuitously or for some associated disorders. On two occasions compressive disorders have been reported [1,8], and in both cases the AUSPV has been considered to be responsible for a bronchial compression. This occurred in children aged 2 months and 6 years respectively.…”
Section: Fig 2 Pulmonary Angiogram Anteroposterior Projection Venmentioning
confidence: 99%
“…The few reported cases of pulmonary varix in infants and an association with other developmental defects supports a congenital etiology [2][3][4]. Several authors have hypothesized that the defect occurs at the time of embryonic transition from splanchnic to pulmonary venous drainage [5] .…”
mentioning
confidence: 99%