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1.
AJR Am J Roentgenol ; 214(1): W1-W10, 2020 01.
Artículo en Inglés | MEDLINE | ID: mdl-31593515

RESUMEN

OBJECTIVE. Imaging plays an important role in the diagnosis and staging of malignancies. Many common lymphoproliferative and other solid tumor malignancies can be viral-related. CONCLUSION. This review discusses the imaging findings that can be associated with common viral-induced malignancies. Knowledge of these imaging presentations can help narrow the differential diagnosis to reach a specific diagnosis through a precise workup and proper management.


Asunto(s)
Neoplasias/diagnóstico por imagen , Neoplasias/virología , Virosis/complicaciones , Neoplasias del Ano/diagnóstico por imagen , Neoplasias del Ano/virología , Linfoma de Burkitt/diagnóstico por imagen , Linfoma de Burkitt/virología , Carcinoma Hepatocelular/diagnóstico por imagen , Carcinoma Hepatocelular/virología , Femenino , Enfermedad de Hodgkin/diagnóstico por imagen , Enfermedad de Hodgkin/virología , Humanos , Neoplasias Hepáticas/diagnóstico por imagen , Neoplasias Hepáticas/virología , Masculino , Neoplasias Orofaríngeas/diagnóstico por imagen , Neoplasias Orofaríngeas/virología , Neoplasias del Pene/diagnóstico por imagen , Neoplasias del Pene/virología , Sarcoma de Kaposi/diagnóstico por imagen , Sarcoma de Kaposi/virología , Neoplasias del Cuello Uterino/diagnóstico por imagen , Neoplasias del Cuello Uterino/virología
2.
J Pediatr Hematol Oncol ; 36(1): 62-5, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23619114

RESUMEN

We report the case of a 2-year-old Lebanese male child, known to have congenital factor XIII (FXIII) deficiency, who presented to the emergency department with somnolence and projectile vomiting without any head trauma. He has been on a prophylactic dose of 10 IU/kg of FXIII concentrate every 4 weeks since birth, but he missed his last 2 doses due to shortage of supply. Imaging studies showed an epidural hematoma with a midline shift. The child was started on 20 IU/kg of FXIII replacement, and a left parietal craniotomy was performed immediately. He tolerated the surgery well with an uneventful postoperative course. Previous DNA analysis carried out for the family members detected a small deletion (c.1475-1476delGA) in exon 12 in this child and his eldest brother. This mutation has been previously reported once in another Lebanese child with FXIII deficiency who presented with spontaneous splenic rupture. To the best of our knowledge, this is the first case of acute nontraumatic spontaneous epidural hematoma in a child with congenital FXIII deficiency. Furthermore, patients on FXIII replacement therapy have less bleeding events, thus lifelong adherence to the prophylaxis is essential to decrease the morbidities and the mortalities associated with FXIII deficiency, most notably intracranial hemorrhages.


Asunto(s)
Deficiencia del Factor XIII/complicaciones , Hematoma Epidural Craneal/sangre , Hematoma Epidural Craneal/etiología , Preescolar , Servicios Médicos de Urgencia , Factor XIII/genética , Factor XIII/uso terapéutico , Deficiencia del Factor XIII/tratamiento farmacológico , Deficiencia del Factor XIII/genética , Hematoma Epidural Craneal/cirugía , Humanos , Masculino
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