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 continuously improved upon by countless contributing members. Our dedicated editors oversee each edit for accuracy and style. Find out more about articles.
73 results found
Article
Carotidynia
Carotidynia, also known as Fay syndrome, is a rare syndrome characterized by neck pain in the region of the carotid bifurcation.
It was classified by the International Headache Society (IHS) in 1988 as an idiopathic neck pain syndrome associated with tenderness over the carotid bifurcation with...
Article
Eagle syndrome
Eagle syndrome refers to symptomatic elongation of the styloid process or calcified stylohyoid ligament 1,2. It is often bilateral. In most cases, the cause is unknown; however, the condition is sometimes associated with disorders causing heterotopic calcification such as abnormal calcium/phosph...
Article
Inferior vena cava obstruction
Inferior vena cava obstruction, also known as inferior vena cava syndrome, refers to the clinical manifestations occurring as a result of any blockage in the inferior vena cava. It can occur due to external compression, thrombosis of inferior vena cava or iatrogenic placement of filters 1. Certa...
Article
Cerebral hyperperfusion syndrome
Cerebral hyperperfusion syndrome is a rare complication seen after treatment of long-standing severe carotid stenosis by carotid endarterectomy or carotid artery stenting. It is believed to be the result of failure of normal cerebral blood flow autoregulation.
Terminology
Cerebral hyperperfus...
Article
Marfan syndrome
Marfan syndrome is a multisystem connective tissue disease caused by a defect in the protein fibrillin 1, encoded by the FBN1 gene. Cardiovascular involvement with aortic root dilatation and dissection is the most feared complication of the disease.
Epidemiology
The estimated prevalence is aro...
Article
Terson syndrome
Terson syndrome refers to intraocular hemorrhage in patients with intracranial hemorrhage.
Terminology
The traditional definition of Terson syndrome was vitreous hemorrhage associated with subarachnoid hemorrhage. However, there is also a broader definition which captures intraocular hemorrhag...
Article
Anterior choroidal artery syndrome
Anterior choroidal artery syndrome is a rare entity caused by cerebral infarction in the anterior choroidal artery territory.
Clinical presentation
In its complete form, the syndrome is characterized by the triad of 7:
contralateral hemiplegia
contralateral hemisensory loss
contralateral ho...
Article
Acute coronary syndrome
Acute coronary syndrome (ACS) is a group of cardiac diagnoses along a spectrum of severity due to the interruption of coronary blood flow to the myocardium, which in decreasing severity are:
ST elevation myocardial infarction (STEMI)
non-ST elevation myocardial infarction (NSTEMI)
unstable an...
Article
Drug rash with eosinophilia and systemic symptoms syndrome
The drug rash with eosinophilia and systemic symptoms (DRESS) syndrome typically manifests as a skin rash, fever, lymph nodal enlargement with variable internal organ involvement, and represents a hypersensitivity reaction to medication.
Clinical presentation
Clinical presentation can be vari...
Article
Parkes Weber syndrome
Parkes Weber syndrome or less commonly F P Weber syndrome is a traditional eponymous denomination of a certain type of angiodysplasia, that would nowadays rather be called a mixed hemolymphatic congenital vascular malformation (CVM) with arteriovenous (AV) shunting, based on the Hamburg classifi...
Article
Superior mesenteric artery syndrome
Superior mesenteric artery (SMA) syndrome, also known as Wilkie syndrome, cast syndrome or aortomesenteric duodenal compression syndrome, is a rare acquired vascular compression disorder in which acute angulation of the superior mesenteric artery (SMA) results in compression of the third part of...
Article
Moyamoya syndrome
Moyamoya syndrome, also termed the moyamoya pattern or phenomenon, is due to numerous conditions that can cause arterial occlusion of the circle of Willis, with resultant collaterals, and appearances reminiscent of moyamoya disease.
These conditions include 1-4 :
vessel wall abnormalities
int...
Article
Carney complex
Carney complex (not to be confused with the Carney triad) is a rare multiple endocrine neoplasia syndrome characterized by 1-4:
cardiac myxoma
often multiple
seen in two-thirds of patients with Carney complex
skin pigmentation (blue nevi): especially of the face, trunk, lips, and sclera
M...
Article
Familial multiple cavernous malformation syndrome
The familial multiple cavernous malformation syndrome, or familial cerebral cavernous malformation syndrome, is uncommon, accounting for only a minority of cavernous malformations.
Epidemiology
It has been more frequently reported in patients of Hispanic descent 1.
Diagnosis
The definition o...
Article
Achenbach syndrome
Achenbach syndrome, also known as paroxysmal finger hematomas or acute idiopathic blue finger, is a rare disorder characterized by spontaneous rupture of digital arteries with resultant hematomas 1-3.
Epidemiology
Achenbach syndrome is more common in women, typically in middle to older age (30...
Article
Williams syndrome
Williams syndrome (WS), sometimes called Williams-Beuren syndrome, is characterized by some or all of the following features:
craniofacial dysmorphism (e.g. elfin facies)
oral abnormalities
short stature (50% of cases)
mild to moderate intellectual disability
supravalvular aortic stenosis ...
Article
Wyburn-Mason syndrome
Wyburn-Mason syndrome (also known as Bonnet-Dechaume-Blanc syndrome) is a rare, nonhereditary neurocutaneous disorder that typically presents with unilateral vascular malformations that primarily involve the brain, orbits and facial structures. It is currently classified as a cerebrofacial arter...
Article
Superior vena cava obstruction
Superior vena cava obstruction (SVCO) can occur from extrinsic compression, intrinsic stenosis, or thrombosis of the superior vena cava. Malignancies are the main cause and are considered an oncologic emergency. Superior vena cava syndrome (SVCS) refers to the clinical syndrome with symptoms tha...
Article
Klippel-Trénaunay syndrome
Klippel-Trénaunay syndrome is a very rare congenital disorder that is characterized by a triad of venous malformations, cutaneous capillary malformations, and limb overgrowth. It is considered an angio-osteo-hypertrophic syndrome.
Terminology
The name Klippel-Trénaunay-Weber syndrome is mislea...
Article
Arterial tortuosity syndrome
Arterial tortuosity syndrome (ATS) is a very rare autosomal recessive connective tissue disease. It is similar to Ehlers-Danlos syndrome (EDS), the major differentiator being the general tortuous nature of the larger arteries.
Clinical presentation
It presents similarly to other collagen disor...
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