Gouverneur's syndrome | |
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Specialty | Urology |
Gouverneur's syndrome is characterised by vesicointestinal fistula with associated suprapubic pain, urinary frequency, pain on passing urine, and tenesmus. [1] [2] It is named after French physician R. Gouverneur. [3]
Interstitial cystitis (IC), also known as bladder pain syndrome (BPS), is a type of chronic pain that affects the bladder and pelvic floor. Together with CP/CPPS, it makes up urologic chronic pelvic pain syndrome (UCPPS). Symptoms include feeling the need to urinate right away, needing to urinate often, and pain with sex. IC/BPS is associated with depression and lower quality of life. Many of those affected also have irritable bowel syndrome and fibromyalgia.
Ehlers–Danlos syndromes are a group of rare genetic connective-tissue disorders. Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation. These can be noticed at birth or in early childhood. Complications may include aortic dissection, joint dislocations, scoliosis, chronic pain, or early osteoarthritis.
A fistula is an abnormal connection between two hollow spaces, such as blood vessels, intestines, or other hollow organs.
Mirizzi's syndrome is a rare complication in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common hepatic duct, resulting in obstruction and jaundice. The obstructive jaundice can be caused by direct extrinsic compression by the stone or from fibrosis caused by chronic cholecystitis (inflammation). A cholecystocholedochal fistula can occur.
Bruit, also called vascular murmur, is the abnormal sound generated by turbulent flow of blood in an artery due to either an area of partial obstruction or a localized high rate of blood flow through an unobstructed artery.
The VACTERL association refers to a recognized group of birth defects which tend to co-occur. Note that this pattern is a recognized association, as opposed to a syndrome, because there is no known pathogenetic cause to explain the grouped incidence.
Reactive arthritis, formerly known as Reiter's syndrome, is a form of inflammatory arthritis that develops in response to an infection in another part of the body (cross-reactivity). Coming into contact with bacteria and developing an infection can trigger the disease. By the time the patient presents with symptoms, often the "trigger" infection has been cured or is in remission in chronic cases, thus making determination of the initial cause difficult.
Vesicovaginal fistula (VVF) is a subtype of female urogenital fistula (UGF).
A vesicointestinal fistula is a form of fistula between the bladder and the bowel.
Acrodermatitis enteropathica is an autosomal recessive metabolic disorder affecting the uptake of zinc through the inner lining of the bowel, the mucous membrane. It is characterized by inflammation of the skin (dermatitis) around bodily openings (periorificial) and the tips of fingers and toes (acral), hair loss (alopecia), and diarrhea. It can also be related to deficiency of zinc due to other, i.e. congenital causes.
In nephrology, vascular access steal syndrome is a syndrome caused by ischemia resulting from a vascular access device that was installed to provide access for the inflow and outflow of blood during hemodialysis.
Abdominal angina is abdominal pain after eating that occurs in individuals with ongoing poor blood supply to their small intestines known as chronic mesenteric ischemia. Although the term angina alone usually denotes angina pectoris, angina by itself can also mean "any spasmodic, choking, or suffocative pain", with an anatomic adjective defining its focus; so, in this case, spasmodic pain in the abdomen. Stedman's Medical Dictionary Online defines abdominal angina as "intermittent abdominal pain, frequently occurring at a fixed time after eating, caused by inadequacy of the mesenteric circulation resulting from arteriosclerosis or other arterial disease. Synonym: intestinal angina."
Benjamin Syndrome is a type of multiple congenital anomaly/intellectual disability (MCA/MR) syndrome. It is characterized by hypochromic anemia with intellectual disability and various craniofacial and other anomalies. It can also include heart murmur, dental caries and splenic tumors.
Édouard Brissaud was a French physician and pathologist. He was taught by Jean Martin Charcot at Pitié-Salpêtrière Hospital. He had interests in a number of medical disciplines including motion disturbances, anatomy, neurology and psychiatry. He died of a brain tumour, aged 57.
A preauricular sinus is a common congenital malformation characterized by a nodule, dent or dimple located anywhere adjacent to the external ear. Frequency of preauricular sinus differs depending the population: 0.1–0.9% in the US, 0.9% in the UK, and 4–10% in Asia and parts of Africa.
Parkes Weber syndrome (PWS) is a congenital disorder of the vascular system. It is an extremely rare condition, and its exact prevalence is unknown. It is named after British dermatologist Frederick Parkes Weber, who first described the syndrome in 1907.
Olga Imerslund was a renowned Norwegian paediatrician, best known for her contribution to identification and naming of the Imerslund-Gräsbeck syndrome.
Katharine Krom Merritt was an American physician specializing in pediatrics. The Kasabach–Merritt syndrome is named after Haig Kasabach and her. She was also a member of the International Society for the History of Medicine (ISHM).
Friedrich Wilhelm Erich Leschke was a German internist.