Articles

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More than 200 results
Article

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...
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Occipital condyle syndrome

Occipital condyle syndrome describes the concurrence of unilateral occipital pain and ipsilateral hypoglossal nerve palsy, which localises to pathology affecting an occipital condyle. While occipital condyle syndrome can have many potential causes, it nearly always represents a manifestation of ...
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Intramedullary spinal metastasis

Intramedullary spinal metastases are rare, occurring in ~1% of autopsied cancer patients, and are less common than leptomeningeal metastases. Intramedullary lesions may result from: growth along the Virchow-Robin spaces haematogenous dissemination direct extension from the leptomeninges Epi...
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CA 19-9

CA 19-9 (carbohydrate antigen 19-9 or cancer antigen 19-9) is a serum antigen (monosialoganglioside) that has increased diagnostic use in the management of several malignancies, mainly of hepatopancreaticobiliary origin. It is non-specific, however, and can rise in both malignant and non-maligna...
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Angiomatoid fibrous histiocytoma

Angiomatoid fibrous histiocytomas (AFH) or angiomatoid fibrous malignant histiocytomas are neoplasms of intermediate biologic potential and are classified as soft tissue tumours of uncertain differentiation. Epidemiology Angiomatoid fibrous histiocytomas a rare and account for about 0.3% of al...
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Choriocarcinoma

Choriocarcinoma is an aggressive, highly vascular tumour. When it is associated with gestation, it is often considered part of the spectrum of gestational trophoblastic disease; it is then termed gestational choriocarcinoma. When it occurs in the absence of preceding gestation, it is termed non-...
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Incidentaloma

An incidentaloma is a radiological neologism to denote a lesion found incidentally and of dubious clinical significance. Although it can refer to any incidental lesion (e.g. pituitary 3, thyroid 4), it is most often used to denote an incidental adrenal lesion, which is commonly an adrenal adenom...
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Jugulodigastric lymph nodes

The jugulodigastric lymph nodes, also known as subdigastric lymph nodes, are deep cervical nodes located below the posterior belly of the digastric muscle and anterior to the internal jugular vein. They are located in neck node level IIa and receive lymphatic drainage from the tonsils, pharynx,...
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Prostate Imaging-Reporting and Data System (PI-RADS)

PI-RADS (Prostate Imaging–Reporting and Data System) is a structured reporting scheme for multiparametric prostate MRI in the evaluation of suspected prostate cancer in treatment naive prostate glands. This article reflects version 2.1 (v2.1), published in 2019 and developed by an internationall...
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CSF alpha-fetoprotein

Alpha-fetoprotein (AFP) in the cerebrospinal spinal fluid (CSF) has been reported as a tumour marker for some intracranial tumours with yolk sac elements, and teratoma 1. Interpretation Elevation intracranial yolk sac tumour intracranial embryonal carcinoma congenital CNS tumours with yolk ...
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Fibrolamellar hepatocellular carcinoma

Fibrolamellar hepatocellular carcinoma is a distinct histological variant of hepatocellular carcinoma characterised on microscopy by laminated fibrous layers between the tumour cells. It is important as it has different demographics and risk factors compared to "standard" hepatocellular carcinom...
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Malignant peritoneal mesothelioma

Malignant peritoneal mesothelioma is an uncommon primary tumour of the peritoneal lining. It shares epidemiological and pathological features with - but is less common than - its pleural counterpart, which is described in detail in the general article on mesothelioma. Other abdominal subtypes (a...
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Bing-Neel syndrome

Bing-Neel syndrome is an extremely rare neurological complication of Waldenström macroglobulinaemia 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 macroglobu...
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Ewing sarcoma

Ewing sarcomas are the second most common malignant primary bone tumours 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 o...
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WHO classification of tumours of bone

The World Health Organisation (WHO) classification of bone tumours is the most widely used pathologic classification system for such disorders. The revision, part of the 5th edition of the WHO series, was published in 2020 and is reflected in the article below 1. Classification Chondrogenic tu...
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WHO classification of thymic tumours

The World Health Organisation (WHO) classification of tumours of the thymus is a component of the WHO classification of thoracic tumours, which was published in its 5th edition in 2021 1. It is a pathological classification of thymic epithelial tumours, including thymomas, thymic carcinomas, and...
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CDKN2A/p16

CDKN2A (cyclin-dependent kinase inhibitor 2A) is a tumour suppressor gene that encodes for the p16 protein, involved in the CDK4/6–RB1 cell-cycle pathway 5.  p16 is a widely used immunohistochemical marker indicating expression of the cell cycle protein, which is upregulated by human papillomav...
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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 tumour varies with the age of affected individuals. Over 9...
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Malignant peripheral nerve sheath tumour

Malignant peripheral nerve sheath tumours (MPNSTs) are forms of peripheral nerve sheath tumours occurring either de novo or arising from pre-existing tumours (e.g. neurofibromas, schwannomas etc.). Approximately half of such tumours are seen in individuals with neurofibromatosis type I (NF1), in...
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WHO classification of haematolymphoid tumours

The World Health Organisation (WHO) classification of haematolymphoid tumours is the most widely used pathologic classification system for haematopoietic and lymphoid neoplasms. The 5th edition 1 was published in 2022 and supersedes the 4th edition revised published in 2016. Classification Mye...

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