Pulmonary Surgical Procedures

Fibrosi cistica 2025: stato dell’arte e novità

Maschio M, Grazian F, Traunero A, Ghirardo S, Amaddeo A.

2025/7 — pag. 430-440 — DOI

Cystic Fibrosis is caused by the mutations in the CFTR chloride channel protein and is still one of the most common fatal genetic disease worldwide. It is a multisystem disease but, to date, most of its morbidity and mortality is due to muco-obstruct...

Malformazione polmonare congenita di tipo I con macrocisti Un caso di intervento prenatale e successiva lobectomia toracoscopica

Alboreto E, Borgia P, Florio A, Gallizia A, Perri K, Salvati P, Torre M, Paladini D, Sacco O

2025/2 — pag. 34-36 — DOI

Congenital Pulmonary Airway Malformations (CPAM) are rare lung development anomalies characterised by varying-sized cysts. The majority of affected newborns are asymptomatic at birth, while a small percentage may experience respiratory difficulties. ...

Storia di un murmure vescicolare che non c’è

Varriale G, Greco M, Tamborino A

2021/8 — pag. 259-260 — DOI

The case of a child with basal left recurrent pneumonia is described. A localized bronchomalacia due to a vascular ring was eventually diagnosed....

Uno stridore inspiratorio: tracheomalacia o corpo estraneo?

M. Ficara, G. Russo, G. Cinelli, F. Felici, E. Marastoni, A. Ghidini, E. Iannella, S. Amarri

2020/6 — pag. 139-139 — DOI

Uno stridore a recente insorgenza

G. Lanzoni, F. Maschio, P. Berlese, C. Zanatta, P. Midrio

2019/8 — pag. 206-206

Trapianto di polmone in fibrosi cistica

A. Agrusti, M. Bramuzzo, M. Maschio, A. Ventura

2017/2 — pag. 99-106

Background - Cystic fibrosis (CF) is a rare genetic disease that progressively involves the pancreatic and pulmonary functions: as respiratory failure develops, lung transplantation is the only therapeutic option available nowadays. Objective - Th...

La fibrosi cistica nel 2017

B.M. Assael

2017/2 — pag. 75-77

Riflessioni sulla bronchite cronica protratta Informazione e vaccini

2016/3 — pag. 152-153

La pediatria si è fermata a Idomeni

2016/3 — pag. 151

Un lobo polmonare iperlucente

G. Vieni, S. Pusceddu, L. Mambelli, F. Pugliese, V. Poletti, F. Marchetti

2015/9 — pag. 593-595

The paper describes the case of a 7-year-old female child with a history of chronic cough following an acute respiratory infection and unilateral hyperlucent lung on chest radiograph. The diagnosis was Swyer-James-MacLeod syndrome, based on chara...

Inalazione di corpo estraneo: uno "strano caso"

G.L. Benetti, C. Iozzi, M. Atzeni

2015/1 — pag. 57-58

Foreign body inhalation is a quite common event in chil-dhood, especially during the first years of life. It can cau-se complete airway obstruction and asphyxia resulting from a large object lodged in the trachea or larynx, which require real emergen...

Una bronchiolite rivelatrice

C. De Chiara, F. de Seta, R. Kosova, L. de Seta

2011/4 — pag. 242-246

A case of acute respiratory distress with hypoxia in a 28-day-newborn presenting with the symptoms of bronchiolitis during an epidemic period is described. The persistence of the symptoms associated with a radiological picture of the chest showing ...

Atelettasia da corpo estraneo

A. Pisanti, R. Pisanti

2010/7 — pag. 452-453

Atelettasia ed enfisema lobari:due storie con due immagini a confronto

A. De Cunto, C. Zanchi, M. Gregori, G. Pelos, J. Schleef, F. Marchetti

2010/7 — pag. 446-451

The work compares the cases of two children of the same age (14-15 months) who raise the similar suspect of inhalation of foreign bodies. In the first case the hypothesis was suggested by the radiologic finding of atelectasis. In the second case th...

Dalla diagnosi prenatale al management post-natale delle malformazioni polmonari

F. Gobbo, G. Pelizzo, J. Schleef

2010/2 — pag. 125-126

Congenital pulmonary airway malformations (CPAM) include a wide spectrum of developmental anomalies. Almost 50% of the cases are diagnosed in utero. These appear as hyperechoic, cystic or mixed lesions. Prenatal clinical course varies from seriou...

Patologia quasi rara, in agguato nel nostro quotidiano. Sbagliando si impara.

2008/9 — pag. 595-596

Malformazione adenoido-cistica congenita (CCAM) polmonare

L. Calligaris, A. Trappan, F. Zennaro

2006/9

Condividere le cure al malato di fibrosi cistica: una sfida per il medico di famiglia e per i Centri

G. Mastella

2006/3 — pag. 143-145

L'indimenticabile caso del piccolo esploratore e della mamma investigatrice

R. Semenzato, F. Maschio, M. Chirico

2005/6 — pag. 389-390

La sindrome del lobo medio nel bambino

G. Nocerino

2005/1 — pag. 37-43

Due to its peculiar anatomical structure, the middle lobe is at high risk for atelectasis, which can be partial or total, with or without parenchymal infiltration. Particularly in cases of partial or “pure” atelectasis, antero-posterior X-ray may n...

Acido folico, acido folico, acido folicoLamivudina per l’epatite B cronicaLeucemia linfoblastica acuta: già in utero?Arteriosclerosi prenataleAlti e bassi degli steroidi “prenatali”Vaccini: chi precipita (Parotite-Rubini, Rotavirus) e chi sale (Polio, Morbillo)Indici di infezione: procalcitoninaEpidemiologia delle meningitiFibrosi cistica e trapianto di polmone: sì, ma

1999/9 — pag. 539-540

Un’opacità polmonare impenetrabile

M. Ranieri, U. Corsi, A. Tonetto, G. Dianese, M. Anibali

1999/1 — pag. 53-54

Una tubercolosi antibioticoresistente trattata con gamma-interferone

C. Salvatore

1998/6 — pag. 378

Allergia non vuol dire asma

G. Cavagni, A. Borghi

1997/5 — pag. 325-327