cutaneous hodgkin’s lymphoma is a rare disease (0.5% to 3.4%) which tends to be in the setting of an advanced disease and has a poor prognosis. treatment of patients with cutaneous involvement of hodgkin’s lymphoma is according to dissemination of disease (systemic or localized therapy). the majority of data in this context are based on individual case reports or literature reviews. we have rep...

abstract background involvement of lacrimal apparatus by non hodgkin lymphoma as a first manifestation is extremely rare and only three cases have been reported in children. the purpose of this report is to determine the clinical characteristic of patient with primary involvement of lacrimal apparatus with lymphoma. case presentation a 7-year-old girl with history of tearing, gradually progress...

introduction: a study was made conserning 142 patients who were suffering from gastrointestinal lymphoma, were seen at the department of hematology and oncology, esfahan medical school, during the period 1982-2002. method: all patients had laparotomy, and biopsy of the site lesion. histopathological subtypes were done in the international working formulation. stage groupings were done applying ...

in this study we surveyed the average survival time of the treated hodgkin's lymphoma patients and also the side effects and malignancies occurring secondary to the treatment. this is a retrospective study of patients referring to ahwaz's shafa hospital in a period of 10 years diagnosed with hodgkin's lymphoma without any age restriction. after gathering all their data, we calculated their surv...

background: the clinical presentation of non-hodgkin lymphoma (nhl) varies tremendously depending upon the type of lymphoma and the areas of involvement. nhl can rarely present as an abdominal mass compressing the inferior vena cava. the clinical presentation due to obstruction of inferior vena cava has often been called the inferior vena cava syndrome (ivcs). it can present acutely or chronica...

Langerhans cell histiocytosis (LCH) is a rare neoplasm defined as the proliferation of bone marrow langerhans cells, which is a kind of dendritic cells. The major pathological features of LCH are expression of CD1a and S100 as well as Birbeck granules. Its presentation can differ from a mild bone lesion to a multi-systemic evolved malignant neoplasm; however, the latter outcome is almost rare. ...

Cancer is a complex group of diseases with multiple eventual causes. The underlying causes are not fully known. Thus, learning more about the known causes of cancer is an important issue. Moreover, among these factors, infection and its association to cancers is controversial. Although, it seems that the genome instability of the cells can initiate cancer development. The purpose of this review...

Introduction: Primary gastric lymphoma (PGL) is a rare tumor, whose differential diagnosis may become complicated without precise immunohistochemistry (IHC) and genetic analysis. Case Presentation: A 33-year-old woman presented with gastric cancer and had undergone gastrectomy without precise IHC and staging in another center. Inappropriate IHC after surgery showed diffuse large B-cell lymphom...

background: expression of epstein-barr virus latent member protein-1 (ebv lmp-1) and loss of p16 protein expression are documented in lymphoma, indicating a relationship between them, but this relationship is not clear and sometimes contradictory. thus, this study was conducted to examine the relationship between the loss of p16 and ebv lmp-1 expression in jordanian patients diagnosed with lymp...

  Background and Objective: Inflammatory pseudotumor  is a lesion composed of proliferating spindle cells with mixed inflammatory infiltrates. Some authors have proposed the name inflammatory myofibroblastic tumor as a proper descriptive term rather than the vague inflammatory pseudotumor. The aim of this study was to verify the myofibroblastic origin of spindle cells in idiopathic orbital inf...