2013
DOI: 10.1155/2013/327250
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Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins (ACD/MPV): A Case Series

Abstract: Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is a rare, fatal, developmental lung disorder, which usually presents as persistent pulmonary hypertension of the newborn (PPHN) unresponsive to treatment. The authors present their own experience with three cases admitted during the last 15 years.

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Cited by 9 publications
(14 citation statements)
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“… 1 , 6 , 7 In up to 80% of the cases, associated malformations are found for which surgery is occasionally needed. 3 , 8 14 These malformations predominantly affect the gastrointestinal tract, but also affect the cardiovascular and urogenital system. 2 5 , 9 , 15 , 16 Irrespective of the co-morbidities, the mortality of ACD/MPV is almost 100%.…”
Section: Clinical Presentationmentioning
confidence: 99%
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“… 1 , 6 , 7 In up to 80% of the cases, associated malformations are found for which surgery is occasionally needed. 3 , 8 14 These malformations predominantly affect the gastrointestinal tract, but also affect the cardiovascular and urogenital system. 2 5 , 9 , 15 , 16 Irrespective of the co-morbidities, the mortality of ACD/MPV is almost 100%.…”
Section: Clinical Presentationmentioning
confidence: 99%
“… 1 , 4 , 7 , 10 , 18 , 19 , 21 , 29 An X-ray of the lungs does not show features specific for ACD/MPV, but can show unspecific diffuse haziness or pneumothoraces, most likely caused by mechanical ventilation. 4 , 7 , 10 , 18 , 19 , 29 A computed tomography (CT) scan may show bilateral widespread ground-glass infiltrates with septal line thickening, 12 , 21 while a CT angiography does not result in the diagnosis either due to the limitations of imaging most peripheral capillaries of the lung. Photoacoustic imaging, however, is able to perform molecular imaging at a high resolution inside different tissues and therefore overcomes the limitations of a CT angiography.…”
Section: Diagnosismentioning
confidence: 99%
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“…More recently, more mutations and deletions were found in the FOXF1 gene related to ACD/MPV. 2 , 6 , 11 To date, 40% of all ACD/MPV cases have mutations in the FOXF1 gene 1 , 12 , the majority are de novo mutations, but familial inheritance and siblings’ involvement were also reported in some cases. 13 , 14 , 15 , 16 …”
Section: Discussionmentioning
confidence: 99%