Jejunal duplication presenting with perforation peritonitis: Complication of a rare congenital malformation in an elderly female
نویسندگان
چکیده
Intestinal duplication is a rare congenital malformation that usually detected or becomes symptomatic in early paediatric age and rarely reported adults. The ileum the most frequent site, while jejunum involved. Features are often nonspecific, hence difficult to diagnose. Ultrasonography preferred imaging method. surgical procedure determined depending on presentation. We present case of an adult female presenting with perforation peritonitis. Intraoperatively, approximately 6 cm length communicating jejunal tubular over mesenteric margin was found, involving segment normal jejunum. Resection anastomosis carried out. This presentation proposed further insight into enteric their clinical presentations, along emphasis how why this entity missed preoperatively came out be intra-operative surprise.
منابع مشابه
Nosocomial Jejunal Mucormycosis - an Unusual Cause of Perforation Peritonitis
Mucormycosis is a rare but highly invasive opportunistic fungal infection. Gastrointestinal disease although uncommon is highly fatal. We report a case of jejunal mucormycosis in a 24 year old undernourished female with preceding surgical intervention for acute intestinal obstruction of tubercular etiology. On 8th post-operative day, she developed oozing from suture line, prompting e...
متن کاملA Rare Association of Congenital Asplenia with Jejunal Arteriovenous Malformation
BACKGROUND Isolated congenital asplenia is a poorly understood and rare form of primary immunodeficiency, often associated with life-threatening infections. CASE REPORT We encountered a unique case of a 22-year-old asplenic male who presented with severe iron-deficiency anemia secondary to occult gastrointestinal bleeding since age 15. Our extensive work-up confirmed jejunal arteriovenous malfo...
متن کاملAcalvaria: An Extremely Rare Congenital Skull Malformation
Acalvaria defined as absent skull bones, is an extremely rare congenital anomaly with only a handful of cases reported in literature. In this report we presented a male newborn case of acalvaria referred to our hospital (Shahid Motahari hospital of Urmia, Iran). The condition per se has been described as having high mortality rate. Very few living cases, less than ten, have been reported till now.
متن کاملA Case of Liposarcoma With Peritonitis Due to Jejunal Perforation
A 21-year-old man, who had been treated for congenital dilatation of the bile duct 13 years previously, presented with an acute abdomen. The physical examination suggested peritonitis, and an emergent laparotomy was performed. A perforation was foundin the jejunum approximately 100 cm distal to the ligament of Treitz, followed by resection of a 60-cm jejunal segment. No tumorous lesions were fo...
متن کاملA rare cause of faecal peritonitis: jejunal perforation in a patient undergoing treatment for pulmonary tuberculosis
Abdominal tuberculosis (TB) is a rare but well-documented cause of faecal peritonitis, occasionally occurring in cases where the diagnosis has been delayed, thus resulting in progressive disease. Frequently occurring in the ileo-caecal region, it requires commencement of anti-tubercular regimen and can necessitate surgical intervention. We present a rare case of faecal peritonitis in a young im...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: International journal of case reports in surgery
سال: 2023
ISSN: ['2708-1508', '2708-1494']
DOI: https://doi.org/10.22271/27081494.2023.v5.i1a.76