Publications by authors named "Roberta Trapanese"
Hematological characteristics and hepatobiliary complications of hereditary spherocytosis in a tertiary care pediatric center: optimizing diagnosis and care through local and international networks.
Maria Paola Boaro Giulia Reggiani Mirco D'Agnolo Vania Munaretto Francesco Pozzebon Roberta Trapanese
Front Pediatr
October 2023
Article Synopsis
- Hereditary Spherocytosis (HS) is a congenital red blood cell disorder that leads to varied symptoms, including mild to severe anemia, along with complications related to the liver and spleen.
- The study evaluated pediatric HS patients' diagnosis and management, reviewing medical records from 2010 to 2020, finding that many did not receive necessary confirmatory tests despite early symptoms.
- Results indicated a strong link between HS and hepatobiliary complications like gallstones, emphasizing the need for improved diagnostic pathways and earlier screening to prevent complications.