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Background: Idiopathic mesenteric phlebosclerosis (IMP) is a rare condition that causes ischaemic colitis, has various clinical manifestations, and may even be asymptomatic, often resulting in clinical misdiagnosis.
Case Summary: We report the case of a 44-year-old woman with chief complaints of abdominal pain, vomiting and decreased defecation. One year prior, the patient was asymptomatic and therefore misdiagnosed with inflammatory bowel disease based on incidental findings on an abdominal computed tomography (CT) scan. The present abdominal CT scan revealed an intestinal obstruction, diffuse thickening of the entire colon wall and calcification of the mesenteric and colonic veins. Colonoscopy revealed multiple ulcerations and extensive dark purple discolouration of the oedematous mucosa. Colonic transit studies suggested a decrease in colonic motility. IMP was considered the underlying cause of her pseudoileus, which was potentially linked to her consumption of Chinese medicinal teas for more than 30 years. The patient underwent conservative medical treatment, and her symptoms gradually improved. She exhibited no signs of ileus or other significant discomfort at the outpatient follow-up one year after the discontinuation of Chinese herbal tea consumption.
Conclusion: IMP can present with symptoms of pseudoileus as initial complication. Clinicians can use CT and colonoscopy for differential diagnoses.
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http://dx.doi.org/10.12998/wjcc.v13.i25.105028 | DOI Listing |
A 75-year-old woman had been taking a geniposide-containing herbal medicine for 7 years and was admitted to our hospital for nausea, abdominal pain, and distention. CT revealed colonic wall thickening, whereas CS revealed a dark-purple edematous mucosa. Furthermore, biopsy specimens revealed small vein hyalinization.
View Article and Find Full Text PDFWorld J Clin Cases
September 2025
Department of Gastroenterology, Aerospace Center Hospital, Beijing 100049, China.
Background: Idiopathic mesenteric phlebosclerosis (IMP) is a rare condition that causes ischaemic colitis, has various clinical manifestations, and may even be asymptomatic, often resulting in clinical misdiagnosis.
Case Summary: We report the case of a 44-year-old woman with chief complaints of abdominal pain, vomiting and decreased defecation. One year prior, the patient was asymptomatic and therefore misdiagnosed with inflammatory bowel disease based on incidental findings on an abdominal computed tomography (CT) scan.
Acta Chir Orthop Traumatol Cech
June 2025
Ortopedicka klinika 1. lekarske fakulty Univerzity Karlovy a IPVZ, Fakultni nemocnice Na Bulovce, Praha.
Ischemic complications in the supramesocolic anatomical region with the development of acute pancreatitis due to compression of the celiac artery or superior mesenteric artery are rare but potentially serious complications after major spine surgery. A case report of two patients with idiopathic scoliosis who underwent posterior instrumented correction and fusion with subsequent development of acute pancreatitis due to vascular compression of the retroperitoneum is presented. The manifestation of an acute abdomen within 24 hours after the surgery with elevation of pancreatic obstruction enzymes and confirmation of acute pancreatitis on CT angiography with abdominal pain, gastrectasia, and ileus clinical findings.
View Article and Find Full Text PDFCureus
July 2025
Department of Colorectal Surgery, Monash Health, Melbourne, AUS.
Abdominal apoplexy, or idiopathic spontaneous intraperitoneal hemorrhage (ISIH), is a rare and life-threatening condition caused by the rupture of a mesenteric vessel, leading to massive abdominal bleeding and potential hemodynamic shock. This report presents the case of a 62-year-old patient with hypertension and anticoagulant use who arrived at the emergency department with abdominal and unusual chest pain. Initial imaging did not show signs of bleeding, delaying diagnosis until significant hemodynamic deterioration occurred, necessitating a damage control exploratory laparotomy to evacuate hemoperitoneum and ligate the middle colic artery.
View Article and Find Full Text PDFEuropean J Pediatr Surg Rep
January 2025
Department of Pediatric Surgery, Hôpital des Enfants, CHU Toulouse, Toulouse University, Toulouse, Occitanie, France.
Superior mesenteric artery (SMA) syndrome is a rare cause of proximal bowel obstruction in pediatric surgery. We present the management of a rare, idiopathic, and acute form of SMA syndrome in a teenage girl, successfully treated with a robotic approach. A 14.
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