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Featured researches published by A. Ghiselli.


Biology and medicine | 2017

Helicobacter Pylori Infection: We Should Always Verify the Intrafamilial Transmission

Marco Manfredi; Silvia Iuliano; Pierpacifico Gismondi; Barbara Bizzarri; Federica Gaiani; A. Ghiselli; Gian Luigi de’Angelis

Background and Aims: Helicobacter pylori infection is one of the most common gastrointestinal infections in humans; it affects about 30% of people in developed countries and about 80% in developing ones. The majority of patients acquire the infection during childhood and the intrafamilial transmission is considered one of the most important routes of infection. The aim of this study was to assess the intrafamilial transmission rate among family members of index subjects. Methods: We have suggested all patients H. pylori-positive (99 patients, symptomatic index subjects) diagnosed during 18 months (Sep 2011-Dec 2012) to screen their family members by stool antigen test (SAT) and, when positive, to perform upper gastrointestinal endoscopy. Results: Through SAT we identified 126 patients belonging to 41 households of 99 initial index subjects, therefore 41 index subjects (41.4%) had at least one family member affected. The entire population studied included 225 H. pylori-positive patients: 99 index subjects (symptomatic) and 126 family members diagnosed by SAT screening and histological examination by gastroscopy. Of these, 103 patients (81.7%) were considered slightly symptomatic (mild clinical history until then not important enough to perform further diagnostic study) and 23 patients (18.3%) were totally asymptomatic. Conclusions: In the spread of H. pylori infection, the intrafamilial transmission is an important route of contamination; besides the known mother-to-child dyad, also the transmission among family members plays a considerable role and it should be always verified.


Archives of Disease in Childhood | 2017

P93 Situs viscerum inversus and apple peel atresia: a rare association. case report

E. Manzali; Pierpacifico Gismondi; A. Ghiselli; Barbara Bizzarri; Carmen Madia; Federica Gaiani; Gian Luigi de’Angelis; Daniele Alberti

Background and aims Duodenal atresia is a relatively common anomaly and its frequency ranges from 1 in 3000 to 5000 live births. Association of duodenal atresia with situs viscerum inversus is rare and fewer than 20 patients have been reported in literature. Methods We present a sub-Saharan 1 years old female baby, born at 31 weeks with prenatal diagnosis of situs viscerum inversus with dextrocardia, ventricular septal defect, ductus venous agenesis, duodenal atresia and intestinal malrotation. We considered risk factors, clinical and surgical management, complications and evolution of this rare association. Results A 31 weeks female baby was born by emergency caesarean section for cardiotocographic changes. Her mother history was positive for pre-gestational diabetes on insulin therapy and for Streptococcus beta-haemolytic infection. Incomplete intrapartum amplicillin prophylaxis was made. The baby weighed 2300 g and her Apgar scores were 5 and 5, needing non-invasive ventilation with nCPAP. Because of suspected intestinal obstruction, parental nutrition was started one day after birth and a radiological examination was performed showing the mirror image of a double-bubble configuration of duodenal atresia. She underwent laparotomy at 6 days of life, confirming situs inversus and intestinal necrosis secondary to volvulus on common mesentery (apple peel type 3b): duodeno-cecal anastomosis with saving the ileocecal valve was performed. Histology of the surgical specimen confirmed the transmural necrosis. Six days after, enteral nutrition was progressively introduced with good tolerance and weight gain; parental nutrition was continued with subsequent cholestasis needing the modification of the lipid composition. At 3 months of age, she underwent a Bianchi intestinal lengthening procedure and cholecystectomy. The onset of post-surgical duodenal stenosis two months after required one endoscopic pneumatic dilation (8–10 mm) and a gastrostomy button was placed too. Upper endoscopies performed 1 month and 6 months later were normal. Enteral and parental nutrition was continued and the oral feeding was gradually introduced. Conclusions Duodenal atresia and situs inversus are rare combinations. Outcome is good with appropriate multidisciplinary management and follow-up. Maternal diabetes could be factor risk of laterality, as suggested in literature.


Archive | 2013

Diagnostic Techniques in the Esophagus

Barbara Bizzarri; A. Ghiselli; A. Fugazza; Gian Luigi de’ Angelis

Even in the pediatric age group many diseases can affect the esophageal tract. The only procedure that permits direct visualization of the esophageal mucosa is upper endoscopy. Upper gastrointestinal (GI) endoscopy is employed widely not only for diagnostic but also for therapeutic purposes. This technique allows biopsy collection, which permits confirmation of conditions such as inflammation or infection [1]. Moreover, it permits therapeutic interventions such as dilations, sclerotherapy, endoscopic band ligation, and extraction of foreign bodies.


World Journal of Gastroenterology | 2010

Cystic fibrosis and Crohn's disease: successful treatment and long term remission with infliximab.

F. Vincenzi; Barbara Bizzarri; A. Ghiselli; Nicola de’Angelis; F. Fornaroli; Gian Luigi de’Angelis


Digestive and Liver Disease | 2017

Endoscopic oesophageal dilation in paediatric age: 5 years experience in a tertiary referral hospital

E. Manzali; B. Bizzarri; A. Ghiselli; Silvia Iuliano; G. Nervi; G De Angelis


BMC Pediatrics | 2017

The role of endoscopic ultrasound in children with Pancreatobiliary and gastrointestinal disorders: a single center series and review of the literature

A. Fugazza; Barbara Bizzarri; Federica Gaiani; Marco Manfredi; A. Ghiselli; Pellegrino Crafa; Maria Clotilde Carra; Nicola de’Angelis; Gian Luigi de’Angelis


Digestive and Liver Disease | 2016

P.17.7 DIGESTIVE BLEEDING IN PEDIATRIC AGE: A SINGLE CENTER EXPERIENCE

B. Bizzarri; Federica Gaiani; A. Fugazza; F. Fornaroli; F. Vincenzi; A. Ghiselli; G De Angelis


Digestive and Liver Disease | 2015

Correspondence between PCDAI and SES-CD in pediatric patients with Crohn disease

P. Lugani; G. De Caro; B. Bizzarri; F. Fornaroli; A. Ghiselli; F. Vincenzi; Federica Gaiani; G De Angelis


Digestive and Liver Disease | 2014

Efficacy of infliximab in pediatric ulcerative colitis

Maria Cristina Scorrano; Silvia Iuliano; Antonino Salerno; Federica Gaiani; Francesca Calzolari; Benedetta Cavirani; A. Ghiselli; Barbara Bizzarri; Gian Luigi de’Angelis


Digestive and Liver Disease | 2014

Long and short term complications of percutaneous endoscopic gastrostomy in a pediatric population

Silvia Iuliano; Maria Cristina Scorrano; Antonino Salerno; Federica Gaiani; Benedetta Cavirani; A. Ghiselli; F. Fornaroli; F. Vincenzi; Gian Luigi de’Angelis

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