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Oman Medical Journal. 2017; 26 (3): 335-338
en Inglés | IMEMR | ID: emr-188552

RESUMEN

Primary hepatic lymphoma [PHL] presenting with obstructive jaundice is rare and can mimic a preoperative diagnosis of cholangiocarcinoma. We should consider PHL in patients with radiological hepatic disease with normal serum alpha-fetoprotein and carcinoembryonic antigen levels, and elevated lactate dehydrogenase


We present the case of a 67-year-old male with no significant medical history presented with abdominal pain, jaundice, fever, and abnormal liver function tests. Abdominal sonography and computed tomography scan suggested a diagnosis of obstructive jaundice and cholangitis due to cholangiocarcinoma [Klatskin tumor]


A subsequent liver biopsy diagnosed PHL, and the patient was treated with combination chemotherapy, including rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone [R-CHOP]. PHL should be considered in patients presenting with biliary obstruction


Asunto(s)
Humanos , Masculino , Anciano , Linfoma , Neoplasias Hepáticas , Ictericia Obstructiva/diagnóstico , alfa-Fetoproteínas , Antígeno Carcinoembrionario , Quimioterapia Combinada , Biopsia
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