Guglielmo Paolantonio

Spontaneous closure of an atraumatic cervical spinal arteriovenous fistula in a pediatric patient

Guglielmo Paolantonio, Alessia Carboni, Michela Ada Noris Ferilli, Carlotta Ginevra Nucci et autres

it (code pays fourni par la source)

Multiple pyogenic granulomas on arteriovenous malformation associated with NRAS mutation

Andrea Diociaiuti, Marta Grimaldi, Elisa Pisaneschi, Maria Lisa Dentici et autres

it (code pays fourni par la source)

Tumor ablation in children

Giulia Cassanelli, Guglielmo Paolantonio, George Koshy Parapatt, Gian Luigi Natali

it (code pays fourni par la source)

Fibrolipomatous hamartoma of the median nerve in a child with carpal tunnel syndrome: imaging findings and literature review

Guglielmo Paolantonio, Marco Cirillo, Francesca Grussu, Simona Giancristoforo et autres

it (code pays fourni par la source)

Pediatric liver cirrhosis interventional procedures: from biopsy to transjugular intrahepatic portosystemic shunt

Gian Luigi Natali, Giulia Cassanelli, Guglielmo Paolantonio, George Koshy Parapatt et autres

Cirrhosis is a complex diffuse process whereby the architecture of the liver is replaced by abnormal nodules because of the presence of fibrosis. Several pediatric diseases such as extrahepatic portal vein obstruction, biliary atresia, alpha-1-antitrypsin deficit and autoimmune hepatitis can lead to …

it (code pays fourni par la source)

Percutaneous treatment of chest wall chondroid hamartomas: the experience of a single center

Alessandro Inserra, Cristina Martucci, Giulia Cassanelli, Alessandro Crocoli et autres

BACKGROUND: Thoracic mesenchymal hamartomas are rare benign lesions. Rarely symptomatic, they may compress pulmonary parenchyma, leading to respiratory distress. Although spontaneous regression has been documented, the more common outcome is progressive growth. The treatment of choice is en bloc excision of the …

it (code pays fourni par la source)

Guidelines for Vascular Anomalies by the Italian Society for the study of Vascular Anomalies (SISAV)

Francesco Stillo, Raúl Mattassi, Andrea Diociaiuti, Iria Neri et autres

---

it (code pays fourni par la source)

“De novo” brain arteriovenous malformation in a child with congenital porto-systemic shunt and multisystemic angiomas

Alessandro De Benedictis, Andrea Pietrobattista, Lorenzo Figà Talamanca, Lidia Monti et autres

it (code pays fourni par la source)

Color Doppler Evaluation of Arterial Resistive Index in Infantile Hemangioma: A Useful Parameter to Monitor the Response to Oral Propranolol?

George Koshy Parapatt, Teresa Oranges, Guglielmo Paolantonio, Lucilla Ravà et autres

Infantile hemangioma (IH) is the most common benign vascular tumor in childhood. In more than 85% of all cases, IHs undergo spontaneous involution, but nearly 10-12% of IHs develop complications and require immediate therapy. Oral propranolol is currently the first-line treatment for …

it (code pays fourni par la source)

Vascular Birthmarks as a Clue for Complex and Syndromic Vascular Anomalies

Andrea Diociaiuti, Guglielmo Paolantonio, Mario Zama, Rita Alaggio et autres

Vascular birthmarks are common in neonates (prevalence: 20-30%) and mostly incidental findings sometimes with spontaneous regression (salmon patch and nevus simplex). Capillary malformations are found in about 1% and infantile hemangiomas are found in 4% of mature newborns. Vascular malformations are classified …

it (code pays fourni par la source)

Cutaneous venous malformations as a clue for possible gastrointestinal tract involvement: Diagnosis and treatment of six cases

Andrea Diociaiuti, Roberta Rotunno, Tamara Caldaro, Sabrina Rossi et autres

Venous malformation (VM) is the most common type among vascular malformations classified by the International Society for the Study of Vascular Anomalies. Most VMs are sporadic (94%), caused in 40% of cases by somatic mutation of TEK gene. VMs can be cutaneous, …

it (code pays fourni par la source)

Combined endovascular-surgical treatment for complex congenital intrahepatic arterioportal fistula: A case report and review of the literature

Roberta Angelico, Guglielmo Paolantonio, Monica Paoletti, Chiara Grimaldi et autres

BACKGROUND: Congenital intrahepatic arterioportal fistula (IAPF) is a rare vascular malformation in infants that causes severe portal hypertension (PH) with poor prognosis if untreated. Currently, radiological embolisation is considered the first-line therapy for simple IAPF; however, it might be not resolutive for …

it (code pays fourni par la source)