Research Topics
Species | Antonino TrizzinoSummaryAffiliation: Ospedale dei Bambini G. Di Cristina Country: Italy Publications
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Detail Information
Publications
Simultaneous diagnosis of acute lymphoblastic leukemia and peripheral neuroblastic tumor in a childPaolo D'Angelo
Pediatric Hematology and Oncology Unit, G Di Cristina Children s Hospital, A R N A S Ospedale Civico, Palermo, Italy
J Pediatr Hematol Oncol 34:72-5. 2012..The simultaneous occurrence of 2 different neoplasms in a child is very infrequent, and no comparable cases are reported in the literature...
Severe polyuria and polydipsia in hyponatremic-hypertensive syndrome associated with Wilms tumorPaolo D'Angelo
Unit of Pediatric Hematology and Oncology, G Di Cristina Children s Hospital, A R N A S, Palermo, Italy
Pediatr Blood Cancer 55:566-9. 2010..All HHS signs and symptoms resolved only following surgical resection of the tumor, allowing chemotherapy to be given...
Breast metastases in children and adolescents with rhabdomyosarcoma: Experience of the Italian Soft Tissue Sarcoma CommitteePaolo D'Angelo
Pediatric Hematology and Oncology Unit, G Di Cristina Children s Hospital, Palermo, Italy
Pediatr Blood Cancer 55:1306-9. 2010....
Hepatopathy-thrombocytopenia syndrome (HTS) after actinomycin-D therapy: report of three cases and review of the literaturePiero Farruggia
Pediatric Hematology and Oncology, G Di Cristina Children s Hospital, Italy
Pediatr Hematol Oncol 28:237-43. 2011..We report three children with Wilms tumor, with severe HTS/SOS, but had a different outcome, in spite of vigorous supportive therapy...
Hodgkin lymphoma and nephrotic syndrome in childhoodPiero Farruggia
Unit of Paediatric Haematology and Oncology, G Di Cristina Children Hospital, A R N A S, Via Benedettini 1, 90134, Palermo, Italy
Indian J Pediatr 77:1147-9. 2010..Till date, to the best of author's knowledge, there are about 50 pediatric cases published, no one among Italian children. In the present paper, the authors report 2 cases observed in their department in the 7 yrs period...
Focal nodular hyperplasia of the liver: an unusual association with diabetes mellitus in a child and review of literaturePiero Farruggia
Unit of Pediatric Hematology and Oncology, G, Di Cristina Children s Hospital, and Department of Pediatrics, University of Palermo, Palermo, Italy
Ital J Pediatr 36:41. 2010..We here describe, to our knowledge, the first case of focal nodular hyperplasia in association with diabetes mellitus in childhood...
Castleman's disease in childhood: report of three cases and review of the literaturePiero Farruggia
Unit of Pediatric Hematology and Oncology, G Di Cristina Children s Hospital, ARNAS, Palermo, Italy
Ital J Pediatr 37:50. 2011..There are only about 100 pediatric cases published, five of them in Italy. We report 3 cases of localized Castleman's disease, investigated in our Department in a 3 years period and reviewed the literature...
Hypereosinophilic syndrome in childhood: clinical and molecular features of two casesPiero Farruggia
Pediatric Hematology and Oncology, G Di Cristina Children s Hospital, Palermo, Italy
Pediatr Hematol Oncol 26:129-35. 2009..It is very rare in children. Uncertainties in classification and lack of prospective studies make therapeutic decisions difficult. The authors report two cases of HES in which steroid therapy was effective...
Congenital hepatic fibrosis: a very uncommon cause of pancytopenia in childrenAntonino Trizzino
Onco Ematologia Pediatrica, Ospedale dei Bambini G Di Cristina, Palermo, Italy
J Pediatr Hematol Oncol 27:567-8. 2005..The authors report an unusual case of ARPKD presenting with hepatosplenomegaly and cytopenia mimicking acute leukemia...
Reversible posterior leukoencephalopathy syndrome: report of 2 simultaneous cases in childrenPiero Farruggia
Oncoematologia Pediatrica, Ospedale dei Bambini G. Di Cristina, Palermo, Italy
J Pediatr Hematol Oncol 28:177-81. 2006..A mild left midriasis was the only neurologic defect that persisted in the patient with acute lymphoblastic leukemia...
Mutations affecting mRNA splicing are the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3Alessandra Santoro
Divisione di Ematologia I, A O V Cervello, Palermo, Italy
Haematologica 93:1086-90. 2008..This finding has implications for designing strategies for analysis of the families with suspected familial hemophagocytic lymphohistiocytosis...
