Articles

Articles are a collaborative effort to provide a single canonical page on all topics relevant to the practice of radiology. As such, articles are written and edited by countless contributing members over a period of time. A global group of dedicated editors oversee accuracy, consulting with expert advisers, and constantly reviewing additions.

1,067 results found
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Primary malignancy of the nasopharynx

There are a number of primary malignancies of the nasopharynx: nasopharyngeal carcinoma (squamous cell carcinoma): 70% lymphoma (sinonasal lymphoma): 20% other nasopharyngeal papillary adenocarcinoma adenoid cystic carcinoma mucosal melanoma extramedullary plasmacytoma carcinosarcoma fi...
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Nasopharyngeal carcinoma

Nasopharyngeal carcinomas (NPC) are the most common primary malignancy of the nasopharynx. They are of squamous cell origin. Some types are strongly associated with the Epstein-Barr virus (EBV). Epidemiology Nasopharyngeal carcinoma accounts for ~70% of all primary malignancies of the nasophar...
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Carcinoid tumor

Carcinoid tumors are a type of neuroendocrine tumor that can occur in a number of locations. Carcinoid tumors arise from endocrine amine precursor uptake and decarboxylation (APUD) cells that can be found throughout the gastrointestinal tract as well as other organs (e.g. lung). In general, they...
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Orbital lymphoma

Primary lymphoma of the orbit is one of the most common orbital tumors and accounts for as much as half of all orbital malignancies. It is a B-cell non-Hodgkin lymphoma, and in most cases arises from mucosa-associated lymphoid tissue (MALT). Epidemiology Orbital lymphomas account for only 2% o...
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Gliosarcoma

Gliosarcoma is a classic variant of glioblastoma (along with epithelioid glioblastoma and giant cell glioblastoma) which, although not a distinct diagnosis, remains recognized in the current (2021) WHO classification of CNS tumors as a variant of glioblastoma 9. They are highly malignant (WHO gr...
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Radiation-induced pulmonary fibrosis

Radiation-induced pulmonary fibrosis is the late manifestation of radiation-induced lung disease and is relatively common following radiotherapy for chest wall or intrathoracic malignancies. This article does not deal with the changes seen in the acute phase. Please refer to the article on radi...
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Primary mediastinal large B-cell lymphoma

Primary mediastinal large B-cell lymphoma is a distinct entity, recognized in the WHO classification of lymphoma. Epidemiology Primary mediastinal large B-cell lymphoma accounts approximately 5% of large B-cell lymphoma, which is usually disseminated or found in the abdomen. There appears to b...
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WHO classification of haematolymphoid tumors

The World Health Organization (WHO) classification of haematolymphoid tumors is the most widely used pathologic classification system for hematopoietic and lymphoid neoplasms. The current revision 1, known as the 5th edition, was published in 2022 and supersedes the 4th edition revised published...
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Causes of perfusion defects on a VQ scan

There are several causes leading to a perfusion defect on a VQ scan with an acute pulmonary embolus being only one of them: Vascular causes acute pulmonary embolus previous pulmonary embolus (including fat embolism, thromboembolism, air embolism, tumor) vasculitides affecting the pulmonary v...
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Lymphoma

Lymphoma (historically lymphosarcoma was used for diffuse forms of the disease) is a malignancy arising from lymphocytes or lymphoblasts. Lymphoma can be restricted to the lymphatic system or can arise as extranodal disease. This, along with variable aggressiveness results in a diverse imaging a...
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Teratoma

Teratomas are germ cell tumors that arise from ectopic pluripotent stem cells that fail to migrate from the yolk sac endoderm to the urogenital ridge during embryogenesis. By definition, they contain elements from all three embryological layers: endoderm, mesoderm and ectoderm although frequentl...
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Anterior mediastinal germ cell tumors

Germ cell tumors are one of the causes of an anterior mediastinal mass, and any of the germ cell histologies may be identified. They can therefore be divided histologically into: mediastinal seminoma non-seminomatous germ cell tumors (NSGCT) embryonal carcinoma choriocarcinoma yolk sac tumo...
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Tolosa-Hunt syndrome

Tolosa-Hunt syndrome is an idiopathic inflammatory condition that involves the cavernous sinus and orbital apex and is essentially a clinical diagnosis of exclusion. Epidemiology The estimated incidence of Tolosa-Hunt syndrome is 1 per 1,000,000 person-years with an average age of onset at 41 ...
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Germ cell tumors (mnemonic)

A mnemonic for the differential diagnosis for germ cell tumors is: SECTE Mnemonic S: seminoma E: embryonal cell carcinoma C: choriocarcinoma T: teratoma E: endodermal sinus tumor (yolk sac tumor)
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Von Hippel-Lindau disease

Von Hippel-Lindau (vHL) disease is characterized by the development of numerous benign and malignant tumors in different organs (at least 40 types 1) due to mutations in the VHL tumor suppressor gene on chromosome 3. Epidemiology The disease is rare with an estimated prevalence of 1:35,000-50,...
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Tumors of the chest wall

Tumors of the chest wall are varied, some of which are found most often in this region. They can be divided into benign and malignant tumors and into those which arise in the ribcage and those of soft tissue density. Benign Benign tumors include 1,3,4: soft tissue hemangioma: common lymphan...
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Cancer staging list

Cancer staging involves a number of systems to help direct treatment and aid prognosis. The AJCC TNM staging schema is the most common, but other systems are used for specific malignancies or body parts. Breast breast cancer staging Chest lung cancer staging malignant pleural mesothelioma s...
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WHO classification of thymic tumors

The World Health Organization (WHO) classification of tumors of the thymus is a component of the WHO classification of thoracic tumors, which was published in its 5th edition in 2021 1. It is a pathological classification of thymic epithelial tumors, including thymomas, thymic carcinomas, and ne...
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Metastases to testis

Metastases to testis are a very rare cause of a testicular mass and may be bilateral in up to 15% of patients.  Epidemiology Metastases to the testes are apparent in ~0.04% of autopsy studies in patients with known malignancy. The average age is 57 years, much older than the primary age for pr...
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Testicular cancer

Testicular cancers are the most common malignancy in men between the ages of 20 and 34 years. Epidemiology Testicular cancer is uncommon, accounting for less than 1% of all internal organ malignancies 2. The commonest histology of the tumor varies with the age of affected individuals. Over 90...
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FIGO staging system

The FIGO staging systems are determined by the International Federation of Gynecology and Obstetrics (Fédération Internationale de Gynécologie et d’Obstétrique). In general, there are five stages: stage 0: carcinoma in situ (common in cervical, vaginal, and vulval cancer) stage I: confined to...
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Primary benign cardiac tumors

Primary benign cardiac tumors are much less common than secondary metastatic deposits. However, they are more likely when a cardiac mass is seen outside of the setting of terminal metastatic disease. Tumors include 1,2: cardiac myxoma most common in adults accounts for ~50% of all primary ben...
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Primary cardiac tumors

Primary cardiac tumors are uncommon and comprise only a small minority of all tumors that involve the heart: most are mediastinal or lung tumors that extend through the pericardium and into the heart, or metastases 1. Epidemiology Primary cardiac tumors have an estimated autopsy prevalence of ...
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Male breast cancer

Male breast cancer is exceptionally rare and only accounts for less than 0.25% of male malignancies and ~0.5-1% of all breast cancer (both genders). The diagnosis is sometimes delayed due to the patient's hesitancy to seek advice. Workup from a radiological point of view is the same as for women...
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Breast cancer metastases

Metastases from breast cancer can be a frequent finding in routine oncoradiological practice. Clinical presentation With the universal use and acceptance of screening mammography, the isolated clinical presentation from metastases from breast carcinoma has become rare in clinical practice. His...
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Radial scar

Radial scar, or complex sclerosing lesion, is a rosette-like proliferative breast lesion. It is not related to surgical scarring. Some authors, however, reserve the latter term to lesions over 1 cm 5.  It is an idiopathic process with sclerosing ductal hyperplasia.  Its significance is that it...
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Peripheral primitive neuroectodermal tumor

Peripheral primitive neuroectodermal tumors (pPNET) tend to be large and aggressive retroperitoneal tumors.  Radiographic features The imaging characteristics of peripheral PNETs are non-specific. However, they should be considered in the differential diagnosis of a large, aggressive retroperi...
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Pulmonary metastases

Pulmonary metastases refer to distant tumor spread from a variety of primary tumors to the lungs via the blood or lymphatics. This article primarily describes hematogenous pulmonary metastases while lymphangitic carcinomatosis is discussed separately. Epidemiology Lung metastases are common. ...
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Malignant pleural disease

Malignant pleural disease usually heralds a poor prognosis, whether it represents a primary pleural malignancy or metastatic involvement.  Clinical presentation Clinical presentation is variable. Patients may be asymptomatic or have pleuritic pain. If associated with a sizable pleural effusion...
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Malignant pleural mesothelioma (TNM staging)

Below is the eighth edition of the TNM staging system for malignant pleural mesothelioma, which was published in 2018 1. T - Tumor Tx: primary tumor cannot be assessed T0: no evidence of primary tumor T1 involving ipsilateral parietal pleura (inc. mediastinal and diaphragmatic pleura) +/- v...
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Mesothelioma

Mesothelioma, also known as malignant mesothelioma, is an aggressive malignant tumor of the mesothelium. Most tumors arise from the pleura, and so this article will focus on pleural mesothelioma. Given the presence of the mesothelium in different parts of the body, mesothelioma can arise in var...
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Hodgkin lymphoma (pulmonary manifestations)

Pulmonary manifestations of Hodgkin lymphoma are relatively rare, present in  5-12% of patients at the time of diagnosis. It is relatively more common with the nodular sclerosing subtype. Pulmonary involvement usually indicates stage IV disease.  Radiographic features Bilateral involvement is ...
Article

Calcified mediastinal lymph nodes (differential)

There are numerous causes of calcified mediastinal lymph nodes. Common causes include: infectious granulomatous diseases tuberculosis histoplasmosis sarcoidosis silicosis treated lymphoma Uncommon causes include: Pneumocystis jiroveci (PCP) pneumonia metastases thyroid carcinoma: papi...
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Pheochromocytoma

Pheochromocytomas are an uncommon tumor of the adrenal gland, with characteristic clinical, and to a lesser degree, imaging features. The tumors are said to follow a 10% rule: ~10% are extra-adrenal ~10% are bilateral ~10% are malignant ~10% are found in children ~10% are not associated wit...
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Tuberculosis (intracranial manifestations)

Tuberculosis of the central nervous system can result from either hematogenous spread from distant systemic infection (e.g. pulmonary tuberculosis) or direct extension from local infection (e.g. tuberculous otomastoiditis). Intracranial manifestations of tuberculosis are protean and can affect ...
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POEMS syndrome

POEMS syndrome is the acronymic name for a rare multisystem paraneoplastic disorder including the following features: P: polyneuropathy O: organomegaly E: endocrinopathy M: monoclonal gammopathy S: skin changes Clinical presentation The diagnostic criteria differ from the acronym. Accordi...
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Scleroderma (gastrointestinal manifestations)

Gastrointestinal manifestations of scleroderma can occur in up to 90% of patients with scleroderma 2 with the most common site of gastrointestinal involvement being the esophagus. After skin changes and Raynaud phenomenon, gastrointestinal changes are the third most common manifestation of scler...
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Small cell lung cancer (staging - superseded)

Previously, small cell lung cancer (SCLC) was not staged in the same manner as non-small cell lung cancer (NSCLC), but since 2013 both are staged using the IASLC (International Association for the Study of Lung Cancer) lung cancer staging system (currently in its 8th edition, published in 2016)....
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Small cell lung cancer

Small cell lung cancer (SCLC), also known as oat cell lung cancer, is a subtype of bronchogenic carcinoma separated from non-small-cell lung cancer (NSCLC) as it has a unique presentation, imaging appearances, treatment, and prognosis. Small cell lung cancers are neuroendocrine tumors of the lun...
Article

HIV associated neoplasms

HIV-associated neoplasms are numerous and can be broadly divided into two groups: AIDS-defining malignancies associated but not AIDS defining malignancies AIDS-defining malignancies The development of these malignancies in HIV affected individuals generally implies progression to AIDS...
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Primary uveal malignant melanoma

Malignant uveal melanomas, also referred to as choroidal melanomas, are the most common primary tumor of the adult eye 3.  Epidemiology Malignant melanoma of the uvea is the most common primary intraocular malignancy and is predominantly seen in the White population 5. The incidence of these t...
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Langerhans cell histiocytosis (skeletal manifestations)

The skeleton is the most commonly involved organ system in Langerhans cell histiocytosis (LCH) and is by far the most common location for single-lesion LCH, often referred to as eosinophilic granuloma (EG) (the terms are used interchangeably in this article). For a general discussion of this dis...
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Congenital heart disease chest x-ray (an approach)

With the advent of echocardiography, and cardiac CT and MRI, the role of chest x-rays in evaluating congenital heart disease has been largely relegated to one of historical and academic interest. However, they continue to crop up in radiology exams. In most instances a definite diagnosis cannot ...
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Solitary sclerotic bone lesion

Solitary sclerotic bone (osteosclerotic or osteoblastic) lesions are lesions of bone characterized by a higher density or attenuation on radiographs or computer tomography compared to the adjacent trabecular bone. However, a specific density range has not been specified for those terms 1. Diffe...
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Hepatoblastoma (staging)

As expected there are a number of different staging systems for hepatoblastoma. Staging PRETEXT grouping system of pediatric liver tumors not specific to hepatoblastoma; used in all pediatric liver tumors Intergroup staging system specific for hepatoblastoma (see below) Intergroup staging ...
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Congenital neuroblastoma

Congenital neuroblastoma is defined as neuroblastoma identified within a month of birth, and is divided into: fetal neuroblastoma neonatal neuroblastoma In most cases they present as stage 1, 2 or 4S (see neuroblastoma staging). Fetal neuroblastoma In 90% of cases, fetal neuroblastomas aris...
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Childhood malignancies

Unfortunately the pediatric population is susceptible to malignancies. The most common entities, in overall order of frequency, are 1-4: leukemia/lymphoma: ~35% * acute lymphoblastic leukemia: 23% Hodgkin disease: 5% acute myelogenous leukemia: 4% central nervous system malignancies: ~20% ...
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Neuroblastic tumors

Neuroblastic tumors arise from primitive cells of the sympathetic system and include the following entities: neuroblastoma ganglioneuroblastoma ganglioneuroma These entities represent a spectrum of disease from undifferentiated and aggressive (neuroblastoma) to the well differentiated and la...
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Neuroblastoma (staging)

There are two methods of neuroblastoma staging, one that is based on post-operative patients (INSS) and one developed for pre-treatment patients (INRGSS). Staging International Neuroblastoma Staging System (INSS) This staging system is for post-operative patients and mainly for prognosis 1: ...
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Pleomorphic rhabdomyosarcoma

Pleomorphic rhabdomyosarcoma is a type of rhabdomyosarcoma, and is the least common, accounting for only 5% of all rhabdomyosarcomas. Unlike embryonal and alveolar types, these tumors occur in adults over the age of 40 years 1 and are difficult to distinguish from other pleomorphic sarcomas such...
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Tumors of muscular origin

There are a number of tumors of muscular origin, which overall are relatively uncommon, representing ~2% of benign soft tissue tumors and ~10% of malignant soft tissue tumors 1.  Pathology The tumors can be divided according to the type of muscle fiber: Skeletal muscle origin benign rhabdom...
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Drash syndrome

Drash syndrome, also known as the Denys-Drash syndrome, is associated with an abnormal WT1 gene (Wilms tumor gene) and consists of: Wilms tumor male pseudohermaphroditism progressive glomerulonephritis
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Wilms tumor

Wilms tumor, also known as nephroblastoma, is a malignant pediatric renal tumor. Epidemiology Wilms tumors are the most common pediatric renal mass, accounting for over 85% of cases 1,8 and account for 7% of all childhood cancers 12. They typically occur in early childhood (1-11 years) with pe...
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WAGR syndrome

The WAGR syndrome or complex stands for: Wilms tumors (greatly increased risk) aniridia genitourinary anomalies intellectual retardation (disability) Pathology Genetics Occurs from a mutation related to chromosome 11p13 3 which is in close proximity to the WT1 gene.
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Ewing sarcoma family of tumors

The Ewing sarcoma family of tumors are a group of small round blue cell tumors that are closely histogenetically related, all demonstrating non-random t(11;22)(q24;q12) chromosome rearrangement resulting in the formation of the EWS-ETS fusion gene 1-3.  Terminology Although the literature is l...
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Ewing sarcoma

Ewing sarcomas are the second most common malignant primary bone tumors of childhood after osteosarcoma, typically arising from the medullary cavity with the invasion of the Haversian system. Ewing sarcomas usually present as moth-eaten, destructive, and permeative lucent lesions in the shaft of...
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Synovial sarcoma

Synovial sarcomas are relatively common intermediate-to-high grade malignant soft tissue tumors, often with an initial indolent course, affecting young patients, and most commonly involving the soft tissue surrounding the knees. Epidemiology Synovial sarcomas typically present in adolescents a...
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Krukenberg tumor

Krukenberg tumor, also known as carcinoma mucocellulare, refers to the "signet ring" subtype of metastatic tumor to the ovary. The stomach followed by colon are the two most common primary tumors to result in ovarian metastases, pursued by the breast, lung, and contralateral ovary. Epidemiology...
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Masaoka staging system of thymoma

The Masaoka staging system is commonly adopted for thymomas 1-3, and is the most important determinant of survival following surgical resection 4: stage I: intact thymic capsule stage II: capsular invasion into adjacent mediastinal fat or pleura stage III: macroscopic invasion into adjacent o...
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CNS capillary telangiectasia

CNS capillary telangiectasias are small, asymptomatic low flow vascular lesions of the brain.  Epidemiology As these lesions are asymptomatic, diagnosis usually matches the age of first imaging with MRI, and as such are most frequently found in middle-aged and elderly adults. Their incidence v...
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Undifferentiated pleomorphic sarcoma

Undifferentiated pleomorphic sarcoma (UPS), previously known as malignant fibrous histiocytoma (MFH), is considered the most common type of soft tissue sarcoma. It has an aggressive biological behavior and a poor prognosis. In the majority of cases, undifferentiated pleomorphic sarcoma affects ...
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Primary hepatic lymphoma

Primary hepatic lymphoma (PHL) is very rare, with approximately 100 described cases. If it is being considered as a diagnosis, distant lymphadenopathy, splenomegaly, bone marrow disease, and leukemia should not be present for at least 6 months after the liver tumor has been detected (see: second...
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Kaposi sarcoma

Kaposi sarcoma (KS) is a low-to-intermediate grade mesenchymal tumor that involves the lymphovascular system. The tumor can involve the pulmonary, gastrointestinal, cutaneous and musculoskeletal systems. Although it is often thought of as an AIDS-related condition, it may also be seen in other p...
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Renal cell carcinoma

Renal cell carcinomas (RCC) (historically also known as hypernephroma or Grawitz tumor) are primary malignant adenocarcinomas derived from the renal tubular epithelium and are the most common malignant renal tumor. They usually occur in 50-70-year old patients and macroscopic hematuria occurs in...
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Vertebra plana

Vertebra plana (plural: vertebrae planae), also known as the pancake, silver dollar or coin-on-edge vertebra, is the term given when a vertebral body has lost almost its entire height anteriorly and posteriorly, representing a very advanced compression fracture. Pathology It can occur in a var...
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Askin tumor

The original description of the Askin tumor (by Askin and Rosai in 1979 1), and many studies following it have led to a great deal of confusion. Until recently it has been considered a separate entity or as a type of peripheral primitive neuroectodermal tumor, usually of the chest wall. However...
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Pleuropulmonary blastoma

Pleuropulmonary blastomas are a rare, variably aggressive, childhood primary intrathoracic malignancy. In up to 25% of cases, the mass can be extrapulmonary with attachment to the parietal pleura. They are classified under sarcomatoid carcinomas of the lungs.  Epidemiology Pleuropulmonary blas...
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Dermatomyositis

Dermatomyositis is an autoimmune inflammatory myositis, which like its closely-related condition polymyositis, carries an increased risk of malignancy. Epidemiology There is a recognized female predilection. It has a bimodal age of presentation depending on the variant: juvenile dermatomyosit...
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Brachytherapy

Brachytherapy, also known as sealed source radiotherapy or endocurietherapy, is a form of radiotherapy where a radioactive source is placed, under the guidance of imaging, within or next to the area requiring treatment. This provides localized targeted internal radiation. Brachytherapy has been...
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Localized tenosynovial giant cell tumor

Localized tenosynovial giant cell tumors is a subtype that is most commonly found in the fingers. On imaging, these lesions are commonly demonstrated as localized, solitary, subcutaneous soft tissue nodules, with low T1 and T2 signal and moderate enhancement.  Please see the overview article te...
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Rectal cancer

Rectal cancer, although sharing many of the features of generic colorectal carcinoma (CRC), has different preoperative imaging assessment, with MRI rectum as the mainstay for local staging, and distinct surgical techniques (i.e. total mesorectal excision).  Epidemiology Rectal cancer is genera...
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Rectal cancer (staging)

Staging of rectal cancer uses the TNM staging system and strongly predicts the success, and rate, of local recurrence following rectal cancer resection. MRI is the modality of choice for the staging of rectal cancer, to guide surgical and non-surgical management options. MRI is used at diagnosis...
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Transitional cell carcinoma of the bladder (staging)

Transitional cell carcinoma of the bladder staging uses the TNM system which has replaced the previously widely used Jewett-Strong-Marshall tumor staging system. It is very similar to the staging of TCC of the renal pelvis and staging of TCC of the ureter. TNM staging (8th edition) T Ta: non-...
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Small bowel lymphoma

Small bowel lymphoma is one of the most common small bowel malignancies, accounting for ~25% of all primary small bowel malignancies, and ~40% of all primary gastrointestinal lymphomas. Epidemiology Small bowel lymphoma is most commonly secondary extranodal involvement in widespread systemic l...
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Fibrolamellar hepatocellular carcinoma

Fibrolamellar hepatocellular carcinoma is a distinct histological variant of hepatocellular carcinoma characterized on microscopy by laminated fibrous layers between the tumor cells. It is important as it has different demographics and risk factors compared to "standard" hepatocellular carcinoma...
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Pancreatic metastases

Pancreatic metastases are uncommon and are only found in a minority (3-12%) of patients with widespread metastatic disease at autopsy. They account for only 2-5% of all pancreatic malignancies. Epidemiology Demographics will match those of the primary tumor, but in general, will be in elderly ...
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Raccoon eyes sign (base of skull fracture)

Raccoon eyes sign (or panda eyes in the UK and Ireland) refers to periorbital ecchymosis with sparing of the tarsal plate 3 and is a physical examination finding indicative of a base of skull fracture of the anterior cranial fossa. However it is not pathognomonic for trauma, and there are sever...
Article

Ultrasound appearances of hepatic metastases

Ultrasound appearance of hepatic metastases can have bewildering variation, and the presence of hepatic steatosis can affect the sonographic appearance of liver lesions. Radiographic features Ultrasound Patterns do exist between ultrasound appearance of the hepatic metastases and the likely p...
Article

Hepatic metastases

Hepatic metastases are 18-40 times more common than primary liver tumors 6. Ultrasound, CT, and MRI are helpful in detecting hepatic metastases and evaluation across multiple post-contrast CT series, or MRI pulse sequences are necessary.  Epidemiology The demographics of patients with liver me...
Article

Liver tumors

Liver tumors, like tumors of any organ, can be classified as primary or secondary. Metastases Liver metastases are by far the most common hepatic malignancy, with many of the most common primaries readily seeding to the liver. This is especially the case with gastrointestinal tract tumors, due...
Article

Bethesda criteria of hereditary non-polyposis colorectal cancer

The Bethesda criteria are an alternative to the Amsterdam criteria for the clinical diagnosis of hereditary non-polyposis colorectal cancer (HNPCC).  Diagnosis of HNPCC is made if any of the following criteria are fulfilled: Amsterdam criteria are met 2 or more HNPCC related malignancies  pa...
Article

Linitis plastica

Linitis plastica is a descriptive term usually referring to the appearance of the stomach, although the rectum can also be described this way. The appearance is said to be reminiscent of an old leather water-bottle. Pathology The underlying cause is usually a scirrhous adenocarcinoma with diff...
Article

Gastrointestinal stromal tumor

Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. They account for ~5% of all sarcomas and are mostly found within the stomach and mid-distal small bowel. They respond remarkably well to chemotherapy. Terminology Previously these tumo...
Article

Paragangliomas of the head and neck

Paragangliomas of the head and neck are rare, representing <0.5% of all head and neck tumors. They arise in a number of locations along the carotid sheath and middle ear including the carotid bifurcation, vagal ganglia, jugular bulb, and tympanic plexus. For a general discussion of the patholog...
Article

Pancreatic cancer (staging)

Staging of pancreatic cancer (i.e. ductal adenocarcinoma) is traditionally performed according to the American Joint Committee on Cancer (AJCC) / Union for International Cancer Control (IUCC) TNM system.  In the 2017 new edition (8th edition) AJCC published various major changes including exocr...
Article

Pancreatic ductal adenocarcinoma

Pancreatic ductal adenocarcinoma (PDAC) makes up the vast majority (~90%) of all pancreatic neoplasms and remains a disease with a very poor prognosis and high morbidity. Epidemiology Pancreatic cancer accounts for 22% of all deaths due to gastrointestinal malignancy, and 5% of all cancer deat...
Article

Maxillary antral carcinoma

Maxillary antral carcinomas are an uncommon head and neck malignancy. They usually present late despite growing large since they remain confined to the maxillary sinus and produce no symptoms. Epidemiology Most commonly affects patients over 45 and has a strong male predilection (M:F = 5:1). M...
Article

Cerebral ring enhancing lesions

The differential for peripheral or ring enhancing cerebral lesions includes: cerebral abscess tuberculoma neurocysticercosis metastasis glioblastoma subacute infarct/hemorrhage/contusion demyelination (incomplete ring) tumefactive demyelinating lesion (incomplete ring) radiation necrosi...
Article

Optic nerve enlargement

Enlargement of the optic nerves is uncommon. Swelling of the optic nerves has a surprisingly broad differential. Etiology neoplastic optic nerve glioma optic nerve meningioma leukemia orbital lymphoma metastases juvenile xanthogranuloma medulloepithelioma involvement by retinoblastoma ...
Article

Tram-track sign (orbit)

Tram-track sign refers to the parallel thickening and enhancement around the optic nerve, and is most frequently seen in the setting of optic nerve meningioma. It may, however, also be seen in 1: orbital pseudotumor perioptic neuritis orbital sarcoidosis orbital leukemia orbital lymphoma o...
Article

Sunburst appearance (bone)

Sunburst or sunray appearance describes two separate findings in the bone: a periosteal reaction and a trabeculation pattern. It should not be confused with the sunburst sign of meningioma vascularity.  Sunburst periosteal reaction Sunburst periosteal reaction reflects aggressive periostitis. ...
Article

Cervical lymph node (staging)

Cervical lymph node staging refers to evaluating regional nodal metastasis from primary cancer of the head and neck. The following article reflects the 8th edition of the TNM staging system published by the American Joint Committee on Cancer, which is used for staging starting January 1, 2018 1,...
Article

Papillary tumor of the pineal region

Papillary tumors of the pineal region are one of five pineal parenchymal tumors under the current (2021) WHO classification of CNS tumors with intermediate natural history and a grade of 2 or 3.  Epidemiology Papillary tumors of the pineal region are seen in a wide range of ages, reported from...

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