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Type 1a Duodenojejunal Tubular Duplication Cyst with Complex Rotational Anomaly Masquerading as Chronic Anemia.
J Indian Assoc Pediatr Surg
November 2024
Department of Pediatric Surgery, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Enteric duplication cysts and reversed intestinal rotation (RIR) are rare congenital anomalies, with their coexistence being exceptionally uncommon. We report a 4-year-old girl who presented with chronic anemia and intermittent abdominal symptoms since infancy. Detailed workup for medical causes of anemia was inconclusive.
View Article and Find Full Text PDFAdult Intestinal Malrotation with Atypical Presentation: A Case Report and Diagnostic Challenge.
Am J Case Rep
November 2024
Department of Radiology, Faculty of Medicine, Al-Baha University, Al-Baha, Saudi Arabia.
BACKGROUND A congenital defect known as intestinal malrotation, which has only rarely been described in adults, is most frequently identified in children. For life-threatening consequences, such as intestinal ischemia and death, to be avoided, prompt detection is essential. We report a rare case of adult intestinal malrotation to emphasize the difficulty in diagnosis and surgical treatment.
View Article and Find Full Text PDFMultiple Small Bowel Cavernous Hemangiomatosis: Case Report and Literature Review.
Medicina (Kaunas)
October 2024
General Surgery Department, ASST Lodi-Università Statale di Milano, 20122 Milano, Italy.
Article Synopsis
- A 79-year-old woman was admitted to the hospital due to a month-long history of melena (bloody stools) and anemia caused by chronic gastrointestinal bleeding from cavernous hemangiomatosis in the small bowel.
- She underwent two surgical procedures: an initial laparoscopic jejunal-ileal resection followed by a laparotomic duodenojejunal resection due to ongoing anemia.
- Cavernous hemangiomatosis is a rare condition (7-10% of benign small bowel tumors) that often causes bleeding; diagnosis may involve various imaging techniques, and surgical resection is the preferred treatment method when feasible, considering the risks of extensive surgeries.
Obstructed Right Paraduodenal Hernia: An Unusual Cause of Small Bowel Gangrene.
Cureus
September 2024
General Surgery, Topiwala National Medical College and Bai Yamunabai Laxman Nair Charitable Hospital, Mumbai, IND.
Paraduodenal hernias, especially right sided, are extremely rare entities that are difficult to diagnose due to their uncommon presentation. Some may experience small bowel obstruction. Such patients will have a guarded prognosis if complicated by sepsis due to strangulation or perforation.
View Article and Find Full Text PDFParaduodenal hernia with situs inversus abdominalis: A case report.
Int J Surg Case Rep
November 2024
General Surgery Department, Queen Elizabeth Hospital, Kota Kinabalu, Sabah, Malaysia.
Introduction & Importance: Situs Inversus Abdominalis (SIA) & Paraduodenal Hernias (PDH) are extremely rare causes acute surgical emergencies among adults. We present a case of an adult patient with intestinal obstruction secondary to PDH through the fossa of Landzert with concurrent SIA.
Presentation Of Case: A thirteen-year-old Southeast Asian female with situs inversus abdominalis due to Kartagener syndrome presented with bowel obstruction.
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