Articles

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337 results found
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Red blood cells

Red blood cells (RBCs), also known as erythrocytes (or rarely haematids), are cells that carry oxygen by means of hemoglobin, and form part of the cellular component of blood as it circulates throughout the body. These extremely common cells are typically made in the bone marrow in a process cal...
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Trousseau syndrome

Trousseau syndrome is an inconsistently defined entity which broadly represents the association between thromboembolism and malignancy, often prior to or concomitantly with the diagnosis of the underlying malignancy 1. The syndrome has been variably defined to include entities such as migratory...
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Hematopoietic stem cell transplantation (abdominal complications)

Abdominal complications of hematopoietic stem cell transplantation can occur early (0-100 days) or late (>100 days) post-transplant.  Complications Early bacterial infections, e.g. pseudomembranous colitis fungal infections, often affecting the esophagus or as hepatic/splenic microabscesses ...
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Secondary involvement of the pleura with lymphoma

Secondary involvement of the pleura with lymphoma (secondary pleural lymphoma) is very common, occurring in ~20% of lymphomas. It may be a result of an extension of lymphoma into the visceral or parietal pleura or be a complicating pleural effusion and is a poor prognostic factor.  Epidemiology...
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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...
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Hepatosplenomegaly

Hepatosplenomegaly is simply the simultaneous presence of a pathologically-enlarged liver (hepatomegaly) and spleen (splenomegaly). Pathology Etiology Infection Many infections can produce a mild concurrent enlargement of the liver and spleen. This list is by no means exhaustive. viral EBV...
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Primary ovarian lymphoma

Primary ovarian lymphoma (POL) refers to the involvement of the ovary with lymphoma but without the involvement of any other site. It is an extremely rare yet well-recognized condition. Epidemiology Primary ovarian lymphoma accounts for ~1.5% of ovarian tumors 5. Pathology The rarity of this...
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Pancreatic lymphoma

Pancreatic lymphoma is most commonly a B-cell subtype of non-Hodgkin lymphoma Epidemiology Pancreatic lymphoma is typically seen in middle-aged patients with a mean age of around 55 years old and is more common in immunocompromised patients. Clinical presentation Symptoms are often non-speci...
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Sézary syndrome

Sézary syndrome (SS) is a type of primary cutaneous T-cell lymphoma.  Clinical presentation It is clinically characterized by an extensive erythematous rash covering most of the body as well as the presence of malignant lymphocytes in the blood. History and etymology It is named after Albert...
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Hemolytic uremic syndrome

Hemolytic uremic syndrome (HUS) is a multisystem thrombotic microangiopathic disease characterized by the triad of renal failure, hemolytic anemia and thrombocytopenia. It is the most common cause of renal failure in infancy and childhood requiring dialysis.  There are two forms of this syndrom...
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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 ...
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Primary bone lymphoma

Primary bone (skeletal/osseous) lymphoma (PBL) is a less common manifestation of lymphoma than secondary involvement from disseminated lymphoma. It is rare, accounting for <5% of bone tumors and <1% of non-Hodgkin lymphoma. Terminology PBL is defined as the presence of lymphoma isolated to one...
Article

Idiopathic hypereosinophilic syndrome

Idiopathic hypereosinophilic syndrome (IHES) is a leukoproliferative disorder and refers to a situation when there is an unexplained prolonged eosinophilia with associated organ system dysfunction.  Pathology Individuals have prolonged raised total leukocyte counts with raised eosinophil count...
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Cyanosis

Cyanosis (plural: cyanoses) is a physical sign represented by bluish discolouration of the skin. It indicates there is reduced oxygen bound to red blood cells in the bloodstream. Diagnosis of the underlying cause of cyanosis is based on a thorough history and physical examination. Pathology Et...
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Transient abnormal myelopoiesis

Transient abnormal myelopoiesis (TAM) is a phenomenon that can happen in the fetuses or neonates with trisomy 21. The condition can mimic leukemia. Epidemiology The estimated incidence is at ~10% of newborns with trisomy 21 3. Radiographic features Antenatal ultrasound In the context of kno...
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Birbeck granules

Birbeck granules refer to unusual rod-shaped structures specific to Langerhans cells. Their origin and function remain undetermined. Langerin is a crucial component within Birbeck granules. History and etymology Birbeck granules were first described by Michael S Birbeck in 1961 3. Related pat...
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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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Hyperimmunoglobulin IgE syndrome

Hyperimmunoglobulin E (hyper IgE) syndrome (HIES), also known as Job syndrome, consists of a heterogeneous group of complex hereditary combined B- and T-cell immune deficiency diseases characterized by recurrent Staphylococcus aureus chest infections, characteristic coarse facial appearance and ...
Article

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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Lymphoplasmacytic lymphoma

Lymphoplasmacytic lymphoma (LPL) is an uncommon type of B-cell non-Hodgkin lymphoma. In this condition, the affected tissues (usually bone marrow) become infiltrated by small lymphocytes, plasmacytoid lymphocytes, and plasma cells.  Some publications state this condition synonymous with Waldens...

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