Alessia Bertolino
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Alessia Bertolino has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Alessio Pini Prato
Child Health Department, Pediatric Surgery Unit, Umberto Bosio Center for Digestive Diseases, The Children Hospital, AOU SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy.
1 shared publication - Camilla Pagliara
Umberto Bosio Center for Digestive Diseases, The Children Hospital, AOU SS Antonio e Biagio e Cesare Arrigo, Spalto Marengo, 46, 15121, Alessandria, Italy
1 shared publication - Giulia Mottadelli
Unit of Pediatric Surgery, Umberto Bosio Center for Digestive Diseases, The Children Hospital, AOU SS Antonio e Biagio e Cesare Arrigo, Alessandria, Italy
1 shared publication Marta Erculiani
Umberto Bosio Center for Digestive Diseases, The Children Hospital, AOU SS Antonio e Biagio e Cesare Arrigo, Spalto Marengo, 46, 15121, Alessandria, Italy
1 shared publication- Paola Lago
Neonatal Intensive Care Unit, Critical Care Department, Ca’ Foncello Regional Hospital, Treviso, Italy
1 shared publication - Paola Midrio
Pediatric Surgery, Ca' Foncello Hospital, Treviso, Italy
1 shared publication
Latest Publications
- 23 February 2026
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 61 (6) , 163036
Skip segment Hirschsprung Disease: Unicentric experience with four cases and systematic literature review
- 23 February 2026
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 61 (6) , 163036
Skip segment Hirschsprung Disease: Unicentric experience with four cases and systematic literature review
- Open Access
Congenital Pulmonary Airway Malformation in Preterm Infants: A Case Report and Review of the Literature
Congenital pulmonary airway malformations (CPAMs) represent a well-known cluster of rare lung malformations affecting 1 in 2500 live births. The natural history of many CPAMs is to increase their size in the second trimester, reach a plateau, and, in about 50% of cases, regress and to become barely detectable during the third trimester. Little is known about cases of affected neonates born prematurely: only six cases are described in the literature, recording different conduct and outcomes. Herein, we report the case of a very low birth weight infant born at GW 28 without antenatal findings and presenting at birth with severe respiratory distress, requiring ventilation. Chest X-rays and a CT scan showed the presence of a solid mass in the left lung. An initial conservative approach was adopted as the baby gained respiratory stability within the first days of life. Routine ultrasound (US) showed a progressive reduction of the lesion, mimicking the process of involution that CPAM can exhibit during late gestation. The rarity of the condition does not allow the formulation of any suggestions regarding one type of management over the other. An initial conservative approach seems to be appropriate with regards to the outcome and possible intra- and post-operative complications.
Open AccessCongenital Pulmonary Airway Malformation in Preterm Infants: A Case Report and Review of the Literature
Congenital pulmonary airway malformations (CPAMs) represent a well-known cluster of rare lung malformations affecting 1 in 2500 live births. The natural history of many CPAMs is to increase their size in the second trimester, reach a plateau, and, in about 50% of cases, regress and to become barely detectable during the third trimester. Little is known about cases of affected neonates born prematurely: only six cases are described in the literature, recording different conduct and outcomes. Herein, we report the case of a very low birth weight infant born at GW 28 without antenatal findings and presenting at birth with severe respiratory distress, requiring ventilation. Chest X-rays and a CT scan showed the presence of a solid mass in the left lung. An initial conservative approach was adopted as the baby gained respiratory stability within the first days of life. Routine ultrasound (US) showed a progressive reduction of the lesion, mimicking the process of involution that CPAM can exhibit during late gestation. The rarity of the condition does not allow the formulation of any suggestions regarding one type of management over the other. An initial conservative approach seems to be appropriate with regards to the outcome and possible intra- and post-operative complications.