Plasmablastic lymphoma is a rare and a relatively new entity that was first described in the jaws and the oral cavity of HIV-AIDS patients. We report a case of plasmablastic lymphoma involving the liver in an AIDS patient. Plasmablastic lymphoma is considered a diffuse large B-cell lymphoma with a unique phenotype and predilection for the oral cavity. The case presented had a unique hepatic les...

Different hepatic and biliary tract disorders may occur with celiac disease. Some have been hypothesized to share genetic or immunopathogenetic factors, such as primary biliary cirrhosis, primary sclerosing cholangitis, and autoimmune hepatitis. Other hepatic changes in celiac disease may occur with malnutrition resulting from impaired nutrient absorption, including hepatic steatosis. In additi...

Primary hepatic non-Hodgkin's lymphoma (NHL) is an extremely rare disease that is commonly neglected as a possible diagnosis. The present study reports the case of a middle-aged male with chronic hepatitis B in which primary hepatic NHL and rectal cancer occurred simultaneously. A large solitary tumor in the left lobe of the liver was incidentally detected on routine examination prior to the la...

Systemic EBV+ T cell lymphoma of childhood manifests as a rapidly progressive, life-threatening disorder with fulminant clinical course. Of obscure aetiology, systemic may arise in concurrence primary Epstein Barr viral infection wherein infiltrating lymphocytes demonstrate monoclonal rearrangements within receptor (TCR) genes. delineates virus infected cytotoxic CD8+ or activated CD4+ cells an...

Primary hepatic extranodal mucosa-associated lymphoid tissue (MALT) lymphoma is seen extremely rare compromising 0,016% among non-Hodgkin lymphomas. Association of chronic inflammatory conditions or infectious processes mostly hepatitis B virus (HBV) infection has been reported by scarce number case presentations. Whereas MALT accompanied echinococcus granulosus was described only in one primar...

Citation: Taylor DF, Cho RS, Hall J, Walton D, Womeldorph CM (2016) Hepatic Dysfunction as Presenting Manifestation of Hodgkin’s lymphoma. J Gastroenterol Compl 1(1): 103 Volume 1 | Issue 1 Journal of Gastroenterology and Its Complications Introduction Hepatic dysfunction is rarely the presenting feature of malignancy, however it is important to recognize early on as the quick institution of ch...

Systemic EBV+ T cell lymphoma of childhood manifests as a rapidly progressive, life-threatening disorder with fulminant clinical course. Of obscure aetiology, systemic may arise in concurrence primary Epstein Barr viral infection wherein infiltrating lymphocytes demonstrate monoclonal rearrangements within receptor (TCR) genes. delineates virus infected cytotoxic CD8+ or activated CD4+ cells an...

We present a case of a 60-year-old woman with history of follicular lymphoma in remission presenting for an 18F-fluorodeoxyglucose positron emission tomography/computed tomography for suspected recurrence. Imaging showed widespread hypermetabolic lymphadenopathy consistent with lymphoma recurrence. A 3-month 18F-fluorodeoxyglucose positron emission tomography/computed tomography follow-up after...

Primary hepatic lymphoma (PHL) is an uncommon lymphoid tumor with varied clinical features and treatment outcome. In the present study, the case of a 56-year-old patient with PHL and no clinical presentation was reported. During a routine physical examination, multiple hypodense nodules were incidentally detected in right lobes of the liver and hepatic portal in an abdominal computed tomography...