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1.
Minerva Pediatr ; 70(1): 35-45, 2018 Feb.
Article in English | MEDLINE | ID: mdl-25926159

ABSTRACT

BACKGROUND: Hepatic focal lesions in the pediatric age group are diverse and can be broadly classified into congenital, neoplastic and infective. The aim of this paper was to describe the frequency, nature and clinical presentation of focal hepatic lesions from a pediatric hepatologist perspective. METHODS: Data were retrieved from files of all cases with focal hepatic lesions presenting to the Pediatric Hepatology Unit, Cairo University Pediatric Hospital, from January 2006 to December 2013, after the study protocol was approved by the department research committee and the institution ethical committee. RESULTS: Over an 8-year period, 38 cases had focal hepatic lesions. They constituted less than 1% of the 4475 new cases presenting to the unit over this period. The commonest lesion was hepatic hemangioma(s) (34%). Two-thirds were neoplastic lesions whether benign or malignant. Eighty percent were benign focal lesions. Infectious causes (fascioliasis and pyogenic liver abscess) accounted for 29% of cases. Hepatocellular carcinoma was the commonest malignant neoplasm; it occurred in 5 cases (13.2%) on top of a chronic liver disease. Hepatoblastoma was less common. CONCLUSIONS: From the hepatologist perspective, pediatric focal hepatic lesions are more likely to be benign. Hepatic hemangiomas are the commonest. Infectious causes are common in a developing country like Egypt. Hepatocellular carcinoma is the commoner malignant neoplasm and usually develops on a diseased liver. Screening infants and children with chronic liver disease for development of hepatocellular carcinoma is mandatory. Hepatoblastoma is less likely to present to the pediatric hepatologist as it is referred immediately to the oncologist or onco-surgeon.


Subject(s)
Carcinoma, Hepatocellular/diagnosis , Liver Diseases/diagnosis , Liver Neoplasms/diagnosis , Liver/pathology , Carcinoma, Hepatocellular/epidemiology , Carcinoma, Hepatocellular/pathology , Child , Child, Preschool , Chronic Disease , Egypt/epidemiology , Female , Gastroenterologists , Hemangioma/diagnosis , Hemangioma/epidemiology , Hemangioma/pathology , Hepatoblastoma/diagnosis , Hepatoblastoma/epidemiology , Hepatoblastoma/pathology , Hospitals, Pediatric , Hospitals, University , Humans , Infant , Infant, Newborn , Liver Diseases/epidemiology , Liver Diseases/pathology , Liver Neoplasms/epidemiology , Liver Neoplasms/pathology , Male , Mass Screening/methods
2.
J Interferon Cytokine Res ; 36(1): 1-8, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26406390

ABSTRACT

Combined treatment with pegylated interferon (PEG-IFN)-α2b and ribavirin (RBV) is the only currently approved treatment for hepatitis C virus (HCV) infection in children. The aim of this study was to assess the safety and efficacy of combined treatment with PEG-IFN-α2b and RBV in Egyptian children and adolescents with genotype 4 (GT4) HCV infection. The study included 66 patients (3-17 years of age), of both sexes, infected with HCV GT4, treated with PEG-IFN-α2b (60 µg/m(2)), subcutaneously once weekly plus RBV (15 mg/kg/day) in 2 divided oral doses. Efficacy was assessed by achievement of sustained virological response (SVR). Safety was assessed by questionnaires directed to the patients at specific intervals, growth assessment and laboratory tests. SVR was achieved in 28 patients (42.4%). Nonresponders had significantly commoner history of treated malignancies (P = 0.03), baseline lower absolute neutrophil count (ANC; P = 0.009), higher gamma glutamyl transpeptidase (GGT; P = 0.003), and higher viral load (P = 0.03). Fever was the most frequently reported side effect occurring in 98.5% of the patients followed by musculoskeletal symptoms. Neutropenia was observed in 36 patients (54.6%) and necessitated treatment discontinuation in 1 patient. Decline in both weight and height percentiles was observed in 70% of children who received the combined therapy for a total of 48 weeks. In conclusion, the currently available treatment for HCV GT4 in pediatric patients has modest SVR with numerous adverse events necessitating meticulous monitoring to optimize care of the patients. Side effects could be managed with dose modifications and specific treatment when necessary.


Subject(s)
Antiviral Agents/administration & dosage , Hepacivirus/drug effects , Hepatitis C, Chronic/drug therapy , Interferon-alpha/administration & dosage , Polyethylene Glycols/administration & dosage , Ribavirin/administration & dosage , Adolescent , Antiviral Agents/adverse effects , Body Height/drug effects , Body Weight/drug effects , Child , Child, Preschool , Drug Administration Schedule , Drug Therapy, Combination , Female , Fever/etiology , Fever/pathology , Genotype , Hepacivirus/genetics , Hepacivirus/growth & development , Hepatitis C, Chronic/immunology , Hepatitis C, Chronic/pathology , Hepatitis C, Chronic/virology , Humans , Injections, Subcutaneous , Interferon alpha-2 , Interferon-alpha/adverse effects , Leukocyte Count , Male , Neutropenia/etiology , Neutropenia/pathology , Neutrophils/drug effects , Neutrophils/immunology , Neutrophils/pathology , Polyethylene Glycols/adverse effects , Prospective Studies , Recombinant Proteins/administration & dosage , Recombinant Proteins/adverse effects , Ribavirin/adverse effects , Surveys and Questionnaires , Treatment Outcome , Viral Load/drug effects , gamma-Glutamyltransferase
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