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A mesenteric cyst (MeSH C04.182.473) is a cyst in the mesenterium, and is one of the rarest abdominal tumors, with approximately 822 cases reported since 1507. [1] The incidence is between 1 per 100,000 to 1 per 250,000 hospital admissions. [1] Tillaux's triad named after the French surgeon Paul Jules Tillaux can be
Mesenteric pseudocyst, or pseudomesenteric cyst [1]) is a mass in the abdomen that is devoid of any epithelial lining. [2] They are caused either due to trauma or infection. [ 2 ] [ 3 ] The term mesenteric pseudocyst was first used by Ros et al in 1987.
Macrocystic have cysts greater than 2 cubic centimetres (0.12 cu in), and microcystic lymphatic malformation have cysts that are smaller than 2 cubic centimetres (0.12 cu in). [2] These malformations can occur at any age and may involve any part of the body, but 90% occur in children less than 2 years of age and involve the head and neck.
The extracolonic tumors may include osteomas of the skull, thyroid cancer, epidermoid cysts, fibromas, [4] as well as the occurrence of desmoid tumors in approximately 15% of affected individuals. Desmoid tumors are fibrous tumors that usually occur in the tissue covering the intestines and may be provoked by surgery to remove the colon.
With correct treatment, most cases of amoebic and bacterial dysentery subside within 10 days, and most individuals achieve a full recovery within two to four weeks after beginning proper treatment. If the disease is left untreated, the prognosis varies with the immune status of the individual patient and the severity of disease.
The narrow mesentery predisposes some cases of malrotation to midgut volvulus, a twisting of the entire small bowel that can obstruct the mesenteric blood vessels leading to intestinal ischemia, necrosis, and death if not promptly treated. The fibrous Ladd's bands can constrict the duodenum, leading to intestinal obstruction.
Omphalomesenteric duct cysts (ODC), also known as an omphalomesenteric duct remnant or vitelline cyst, are developmental defects relating to the closure of the omphalomesenteric duct. It usually disintegrates within six weeks of gestation, but remnants of the cyst can sometimes be found along the intestines or umbilicus. Any remnants can be ...
Enteric duplication cysts, sometimes simply called duplication cysts, are rare congenital malformations of the gastrointestinal tract. [1] They most frequently occur in the small intestine, particularly the ileum, but can occur anywhere along the gastrointestinal tract. [1] They may be cystic or tubular in conformation. [2]