Mesenteric lipitis is a rare mesenteric lesion, mainly manifested clinically as abdominal pain and abdominal mass. Dgder described the pathological process of this disease in 1960, pointing out that the disease is caused by a widespread thickening of the mesentery due to nonspecific inflammation, followed by fibrosis, hence it is also known as mesenteric lipomatosis, mesenteric lipogranuloma, primary mesenteric liposclerosis, solitary mesenteric lipodystrophy, retractile mesenteritis, Weber-Christian disease, and idiopathic contractile mesenteritis, etc.
Most patients with this disease have a history of trauma and abdominal surgery, so the occurrence of the disease may be related to abdominal trauma, abdominal surgery, infection, allergy, and other factors. There are many defects that can lead to this disease, and the lesions mainly invade the mesentery, and are more common at the root of the mesentery, and can also spread to the intestinal wall, but are often more limited. Patients generally manifest anorexia, weakness, and weight loss, mainly presenting with abdominal pain, more common in the lower right abdomen, and pain in the left abdomen and upper abdomen can also occur, but less common. The disease has a self-limiting tendency, and general supportive treatment can alleviate the symptoms of the patient.