Primary Hepatic Lymphoma: A Complex and Challenging Diagnosis
نویسندگان
چکیده
منابع مشابه
Primary Hepatic Lymphoma: A Challenging Diagnosis
Introduction. Primary hepatic lymphoma is an unusual malignancy and is very difficult to diagnose promptly. An intrigue case presenting with cholestatic jaundice is reviewed and main disease characteristics are further discussed. Case Report. A 70-year-old male presented with dull right upper quadrant abdominal pain and mild cholestatic jaundice. Initial evaluation revealed mildly elevated live...
متن کامل1 Hepatic Lymphoma Diagnosis
Hematopathology is a rapidly evolving subspecialty in which diagnosis often involves integration of morphology, immunophenotyping, cytogenetics, and molecular data. Many of the recent changes are highlighted in the 2016 revision to the 4th edition of the WHO classification of tumours of hematopoietic and lymphoid tissue. Lineage (i.e. B-cell, T-cell, NK-cell) and maturation (immature vs. mature...
متن کاملPrimary Hepatic Diffuse Large B-Cell Lymphoma in a Patient with Scleroderma
Primary Hepatic Lymphoma (PHL) is rare and possibly associated with viral hepatitis and autoimmune diseases. Scleroderma could exceptionally be complicated by lymphoma. We describe PHL occurring in a 52-year-old female suffering scleroderma for eight years, with no history of cytotoxic or high-dose glucocorticoid therapy. CT scan, performed to work-up abdominal discomfort, constipation, and ...
متن کاملPrimary Hepatic Lymphoma
Primary hepatic lymphoma (PHL) is confined to the liver with no evidence of lymphomatous involvement in other lymphoid structures. It is a very rare malignancy representing less than 1 % of all extra nodal lymphomas. The exact cause of PHL is unknown, but it seems that there is a strong association between hepatitis C virus (HCV) and PHL. The majority of PHL patients are middle-aged men who usu...
متن کاملa rare presentation of primary hepatic lymphoma :a case report
primary hepatic lymphoma (phl) was a rare malignancy usually presenting with abdominal pain, malaise, hepatomegaly, b-symptoms, fatigue, nausea, vomiting and jaundice. it mostly involves liver without any palpable lymphadenopathy and leukemia in peripheral blood smear. on july 22, 2014, a 64 year old man presented with abdominal pain localizing in right upper quadrant and fullness from 2 years ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Medical Journal of Shree Birendra Hospital
سال: 2017
ISSN: 2091-0193,2091-0185
DOI: 10.3126/mjsbh.v16i1.17677