Articles

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336 results found
Article

Hepatic lymphoma

Hepatic lymphoma is a term given to any form of hepatic involvement with lymphoma. This can be broadly divided into: secondary hepatic involvement with lymphoma: most common by far, many tend to be non-Hodgkin lymphoma (NHL) 1 primary hepatic lymphoma: extremely rare Pathology Risk factors f...
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Yttrium-90 ibritumomab tiuxetan

Yttrium-90 ibritumomab tiuxetan, also known by the trade name Zevalin (Acrotech Biopharma LLC, USA), is a theranostic radiopharmaceutical approved for the treatment of patients with relapsed or refractory low grade or follicular non-Hodgkin lymphoma (NHL). More specifically, it is a radioimmunot...
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Diffuse large B-cell lymphoma

Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma. Epidemiology Associations Diffuse large B-cell lymphoma is sometimes associated with immunodeficiency, including acquired immunodeficiency syndrome. Pathology Classification In the 2016 WHO classifica...
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AIDS-related diffuse large B-cell lymphoma

AIDS-related diffuse large B-cell lymphomas are one of the immunodeficiency-associated CNS lymphomas, and in Western countries represented a dramatic increase in primary CNS lymphoma during the HIV/AIDS epidemic of the 1980s, although the incidence is likely lower in patients treated with antire...
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H-shaped vertebra

H-shaped vertebrae, also known as Lincoln log vertebrae, are a characteristic finding of sharply delimited central endplate depression, classically seen in approximately 10% of patients with sickle cell disease, and results from microvascular endplate infarction (Figure 1) 3. It may occasionall...
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Graft versus host disease

Graft versus host disease (GvHD) is a frequent complication of allogeneic hematopoietic stem cell transplantation, commonly known as bone marrow transplantation. Antirejection drugs have reduced the incidence, although it does still frequently occur.  Pathology Graft versus host disease can pr...
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Aplastic anemia

Aplastic anemia is a rare hematopoietic stem-cell disorder. The condition results in pancytopenia and hypocellular bone marrow. Most cases are acquired, however, there are unusual inherited forms. Pathology Aplastic anemia manifests as a marked reduction in the number of pluripotent hematopoie...
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Diffuse T1 bone marrow signal loss

Diffuse T1 vertebral bone marrow signal loss is associated with replacement of fatty marrow by edema or cellular tissue.  Radiographic features MRI T1-weighted imaging without fat suppression is one of the most important sequences for distinguishing between normal and abnormal bone marrow. Ab...
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Peripheral T cell lymphoma

Peripheral T cell lymphoma is an uncommon, heterogeneous group of lymphoma. It can account for around 5-15% of non-Hodgkin lymphoma (NHL). Terminology The word "peripheral" does not mean involvement in the extremities but refers to tumor cells that arise from lymphoid tissue outside of the bon...
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Spleen

The spleen is an organ of the hematological system and has a role in immune response, storage of red blood cells and hematopoiesis. Gross anatomy The spleen is a wedge-shaped organ lying mainly in the left upper quadrant (left hypochondrium and partly in the epigastrium) and is protected by th...
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Tumor lysis syndrome

Tumor lysis syndrome (TLS) is an entity representing a constellation of laboratory and clinical derangements inclusive of: hyperuricemia hyperphosphatemia hypocalcemia and hyperkalemia It is considered an oncological emergency and can occur following treatment of malignancies with high cell...
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Primary pleural lymphoma

Primary pleural lymphoma is extremely rare, especially in immunocompetent patients. Epidemiology Primary pleural lymphoma accounts for <0.5% of all non-Hodgkin lymphoma 2 and ~2.5% of primary chest wall tumors 4.  Pathology Primary pleural lymphoma may be Hodgkin or non-Hodgkin lymphoma with...
Article

Chronic myelomonocytic leukemia

Chronic myelomonocytic leukemia (CMML) is a relatively rare clonal hematologic disorder. In the World Health Organizatiοn classification, it is listed as a disorder with features of both myelodysplastic syndromes and myeloproliferative neoplasms. Clinical presentation Can be variable but many ...
Article

Lymph node enlargement

Lymph node enlargement (rarely lymphadenomegaly) is often used synonymously with lymphadenopathy, which is not strictly correct. Terminology Lymphadenopathy (or adenopathy) is, if anything, a broader term than lymph node enlargement, referring to any pathology of lymph nodes, not necessarily r...
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Splenic lymphoma

Splenic lymphoma, also termed as lymphomatous involvement of the spleen, represents the most common malignancy to involve the spleen. They are commonly secondary, rarely being primary (referred to as primary splenic lymphoma).   This article focuses on the location-specific primary and secondar...
Article

VEXAS syndrome

VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a severe, treatment-refractory, monogenic, multiorgan, autoinflammatory condition with vasculitic and hematological complications. Epidemiology VEXAS syndrome is likely to be rare, but also likely to be underdiagnosed...
Article

Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a rare multisystem disease with a wide and heterogeneous clinical spectrum and variable extent of involvement.  Terminology Langerhans cell histiocytosis was previously known as histiocytosis X. The newer term is preferred as it is more descriptive of its...
Article

Bing-Neel syndrome

Bing-Neel syndrome is an extremely rare neurological complication of Waldenström macroglobulinemia where there is malignant lymphocyte infiltration into the central nervous system (CNS). Epidemiology The exact incidence is unknown, however, in one study of patients with Waldenström macroglobul...
Article

Sickle cell disease (abdominal manifestations)

Abdominal manifestations of sickle cell disease (SCD) are wide and can involve many organs. For a general discussion, please refer to sickle cell disease. Splenic splenomegaly may occur transiently with the sequestration syndrome, where rapid pooling of blood occurs in the spleen, resulting ...
Article

Primary myelofibrosis

Primary myelofibrosis is a myeloproliferative neoplasm in which the bone marrow is replaced with collagenous connective tissue resulting in progressive fibrosis. It is characterized by: extramedullary hematopoiesis progressive splenomegaly anemia variable change in the number of granulocytes...

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