Publications by authors named "Antonella Accinni"

Aim: Foreign body ingestion, particularly that of magnets, is a significant issue for children aged 6 months to 3 years due to their prevalence in toys and household items. Most ingested foreign bodies pass naturally, but 10%-20% of such cases require endoscopic removal, and <1% require surgery.

Case Presentation: A 2-year-old girl presented with abdominal pain, nausea, and vomiting.

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  • Hemoptysis, the coughing up of blood, can stem from various serious underlying conditions, but often involves high-pressure bronchial arteries; Bronchial artery embolization (BAE) is typically the first-line treatment despite varying long-term success rates.
  • A 12-year-old boy with a history of massive hemoptysis underwent multiple BAEs and recent imaging confirmed the location of previous coils; however, he experienced another episode where traditional intervention was complicated by prior treatments.
  • The medical team opted for a thoracoscopic approach, successfully isolating and ligating the problematic vessel, leading to the patient's stabilization and discharge after four days.
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Purpose: Our aim was to explore the applicability of the definition of "large" primary spontaneous pneumothorax (PSP) of adult guidelines to pediatric patients.

Methods: We performed a retrospective monocentric analysis of first-episodes of PSP (Period: January 2010-January 2023). We defined large PSP according to French SPLF/SMFU/SRLF/SFAR/SFCTCV Guidelines.

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  • Patients with complicated appendicitis often experience postoperative complications, leading to the exploration of abdominal drains as a preventative measure.
  • A study evaluated pediatric patients who had appendectomy and compared outcomes between those who had abdominal drains versus those who did not.
  • Results showed that while the drain group had longer hospital stays and time for recovery, there was no significant difference in complication rates, indicating that drains may not provide the expected benefits.
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Introduction: Pectus excavatum, also known as "sunken chest" or "funnel chest," is a congenital condition where the sternum caves inward, creating a noticeable depression in the chest. This deformity can range from mild to severe cases, and can affect appearance and lung and heart function. Treatment options vary depending on the severity of the condition and associated symptoms.

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Background: Laparoscopic appendectomy followed by postoperative intravenous (IV) antibiotics is the standard of care for acute appendicitis and postoperative prevention of intra-abdominal abscesses. The aim of or study was to determine if intraperitoneal irrigation with antibiotics could help prevent intra-abdominal abscess formation after laparoscopic appendectomy for complicated appendicitis in pediatric patients.

Methods: A retrospective study was conducted on consecutive pediatric patients with acute appendicitis who had appendectomy in our Pediatric Surgery Department between August 2020 and February 2022.

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Introduction: International research suggests that poor patient compliance is the main cause of tutor failures in the context of potential novel orthopedic bivalve braces for conservative treatment of pectus carinatum. Our entire experimental study is based on the hypothesis that a rigid bivalve brace that patients can accept could solve the main problem associated with the conservative approach-poor compliance. The hypothesis was to reduce the thickness and weight of the classic bivalve brace to ensure concealment and make it sustainable enough to be worn several hours a day without compromising its therapeutic efficacy.

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  • Midgut volvulus and intussusception are common emergency conditions in children, and this is the first case reported linking the two.
  • An 8-month-old boy presented to the emergency room with abdominal pain and vomiting, where physical exams and lab results indicated serious intestinal issues, including a hard mass and signs of inflammation.
  • During surgery, doctors found a twisted intestinal loop that led to both volvulus and extensive intussusception, resulting in the resection of a significant portion of the ileum.
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Introduction: One of the most prevalent congenital wall abnormalities in children, umbilical hernias are often linked to premature or small-for-gestational-age babies. In cases of intestinal malrotation or if the cecum is very movable, generalized peritonitis may facilitate the imprisonment of these hernias.

Case Report: We described a case of a 4-month-old baby who had a prior reducible umbilical hernia with a history of fever, vomiting, poor appetite, and constipation for around 48 h.

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Introduction: About 95% of congenital chest wall deformities are pectus abnormalities, with pectus excavatum (PE) being the most common. The purpose of this work is to offer a modified Taulinoplasty Technique based on 35 consecutive PE patients' 1-year single-center experience in 2022.

Technique: One minimally invasive procedure for PE is taulinoplasty.

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  • The study focuses on femoral hernia (FH) in children, which is rare and often misdiagnosed, highlighting the need for better management practices in a Tertiary Center.
  • A retrospective analysis from 2010 to 2023 showed 31 pediatric patients underwent FH repair, with a significant pre-operative misdiagnosis rate of 35.5%.
  • The study emphasizes the challenges faced by surgeons, including the variety of surgical approaches and potential complications, stressing the importance of thorough clinical examinations for accurate diagnosis and effective treatment.
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Background And Objectives: Marfan syndrome (MS) is a systemic disease of connective tissues consisting of a variable combination of anomalies. These patients have an increased risk of spontaneous pneumothorax (SP). However, there is a scarcity of pediatric literature on management, and no specific guidelines exist.

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Introduction: The digital chest drainage monitoring system (Medela Thopaz+), unlike analogical systems, reliably regulates the pressure applied to the patient's chest and digitally and silently monitors critical therapeutic indicators (volume of fluid and/or drained air). Its use in adulthood has been widely described, but there is still little experience in the pediatric field. The aim of this study is to test this new device in the pediatric population.

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Background: Described for the first time in 1954, Jeune syndrome (JS), often called asphyxiating thoracic dystrophy, is a congenital musculoskeletal disease characterized by short ribs, a narrow thorax, and small limbs. In this study, we analyzed and presented our preliminary experience with a device for progressive internal distraction of the sternum (PIDS) in patients with symptomatic JS. In addition, we reviewed the contemporary English literature on existing surgical techniques for treating children with congenital JS.

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Background: No age-specific pediatric guidelines exist for the management of spontaneous pneumothorax (SP) in children and adolescents. Treatment remains heterogeneous and center dependent. The role of computed tomography (CT) has yet to be defined.

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Introduction: The prevalence of life-threatening complications (LTCs) related to the minimally invasive repair of pectus excavatum (MIRPE) is unknown and underreported. The aim of this study is to contribute to the real prevalence of these rare but dramatic complications and show what went wrong in order to prevent it in the future.

Case Presentation: A 15-year-old boy affected by pectus excavatum with severe asymmetric deformity of the chest wall was evaluated for elective corrective surgery.

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Uterine leiomyomas are rare in the pediatric population with less than 20 cases in adolescences reported in the literature. Furthermore, these masses represent a common presentation of gynecologic tumors with increasing age. We report a case of a 14-year-old female who presented with abdominal pain and increasing abdominal girth.

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Sigmoid volvulus (SV) is a rare cause of intestinal obstruction in children. Its varied presentation and rapid progression engender a high risk of morbidity and mortality. We report two cases of SV in teenage boys.

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Aim: Paraplegia is an infrequent although fearsome complication of anesthesia and surgical procedures, such as epidural anesthesia and thoracotomy. It may occur in both adults and children and a medullary lesion may be confirmed by magnetic resonance imaging, rather than computed tomography. The aim of this study is to describe the experience of two pediatric tertiary centers, contextualizing it with the other cases reported in literature.

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  • Effective management of vascular access is essential for pediatric cancer patients due to prolonged treatment and the need for frequent blood draws.
  • Central venous catheters play a vital role in providing long-lasting access for administering treatments and preventing painful repeated needle sticks.
  • Understanding the specific techniques for insertion, management, and potential complications of these catheters is crucial to enhance patient outcomes and improve the quality of life for children undergoing cancer treatment.
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Gut involvement is frequent in immunologic disorders, especially with inflammatory manifestations but also with cancer. In the last years, advances in functional and genetic testing have improved the diagnostic and therapeutic approach to immune dysregulation syndromes. CTLA-4 deficiency is a rare disease with variable phenotype, ranging from absence of symptoms to severe multisystem manifestations and complications.

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Introduction: The management of congenital splenic cysts continues to evolve. In the past the standard treatment was splenectomy, but increased knowledge about the spleen's immunologic function has led most pediatric surgeons to preserve splenic tissue. A great number of studies using sclerosing substances have been published, but to date reports in children have been limited.

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We are reporting 3 cases of pediatric endobronchial tumors presented with recurrent pneumonia. The median age of patients, at time of presentation, was 10.6 years.

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Background: Wandering spleen is a rare condition in children that is often caused by loss or weakening of the splenic ligaments. Its clinical presentation is variable; 64% of children with wandering spleen have splenic torsion as a complication.

Objective: To provide up-to-date information on the diagnosis, clinical management and diagnostic imaging approaches for wandering spleen in infants and children and to underline the importance of color Doppler US and CT in providing important information for patient management.

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