Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
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Pagine elettroniche

Quando la sferocitosi incontra il chirurgo

Surgical treatment of hereditary spherocytosis

Chiara Bibalo

Scuola di Specializzazione in Pediatria, IRCCS Materno-Infantile “Burlo Garofolo”, Università di Trieste

Giugno 2015 - pagg. 391 -392

Abstract
Summary Hereditary spherocytosis is a common inherited disorder that is characterized by anaemia, jaundice and splenomegaly. It is reported worldwide and is the most common inherited anaemia in individuals of northern European ancestry. Clinical severity is variable with most of patients having a wellcompensated haemolytic anaemia. Some individuals are asymptomatic, whereas others have severe haemolytic anaemia requiring erythrocyte transfusion. Common complications are cholelithiasis and aplastic crises. Splenectomy is curative and it is indicated in children with moderately-severe and severe hereditary spherocytosis and in patients with symptoms of cholelithiasis.
Suggerite dall'AI
Anemia emolitica Cholecystectomy Cholelithiasis Colecistectomia Hereditary spherocytosis Sferocitosi ereditaria Splenectomia Splenectomy
Classificazione MeSH
Hemic and Lymphatic Diseases Hematologic Diseases Anemia Anemia, Hemolytic (33)
Surgical Procedures, Operative Digestive System Surgical Procedures Biliary Tract Surgical Procedures Cholecystectomy (3)
Digestive System Diseases Biliary Tract Diseases Cholelithiasis (11)
Pathological Conditions, Signs and Symptoms Pathologic Processes Hyperbilirubinemia Jaundice (12)
Hemic and Lymphatic Diseases Hematologic Diseases Anemia Anemia, Hemolytic Anemia, Hemolytic, Congenital Spherocytosis, Hereditary (13)
Surgical Procedures, Operative Splenectomy (13)
Pathological Conditions, Signs and Symptoms Pathological Conditions, Anatomical Hypertrophy Splenomegaly (37)
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Corrispondenza: chiara.bibalo@gmail.com