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JYMS : Journal of Yeungnam Medical Science

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Case report
Synchronous ileal inflammatory fibroid polyp and Meckel’s diverticulum found during laparoscopic surgery for adult intussusception
Sung Il Kang, Mi Jin Gu
Yeungnam Univ J Med. 2020;37(3):226-229.   Published online December 18, 2019
DOI: https://doi.org/10.12701/yujm.2019.00388
  • 8,480 View
  • 100 Download
  • 5 Crossref
AbstractAbstract PDF
We present a rare case of synchronous ileal inflammatory fibroid polyp and Meckel’s diverticulum detected during laparoscopic surgery for adult intussusception. A 48-year-old woman presented with sudden onset of severe abdominal pain. Abdominal computed tomography revealed a segment of ileocecal intussusception. Thus, laparoscopic exploration was performed, which revealed an ileal mass with an outpouching closed luminal structure in the distal ileum. Two abnormal structures were resected via mini-laparotomy, and the patient was discharged without postoperative complications. Histopathological examination confirmed an ileal inflammatory fibroid polyp and Meckel’s diverticulum with ectopic pancreatic tissue.

Citations

Citations to this article as recorded by  
  • Intestinal intussusception of Meckel’s diverticulum, a case report and literature review of the last five years
    Dora Sandoval Schaedlich, Pedro Custodio de Mello Borges, Arnaldo Lacombe, Renato Alonso Moron
    einstein (São Paulo).2023;[Epub]     CrossRef
  • A Rare Cause of Colonic Obstruction: Inflammatory Fibroid Polyp
    Sevinc Dagistanli, Nermin Gunduz, Osman Sibic, Suleyman Sonmez
    Cureus.2022;[Epub]     CrossRef
  • Case Report: Ileo-Ileal Intussusception Secondary to Inflammatory Fibroid Polyp: A Rare Cause of Intestinal Obstruction
    Claudio Guerci, Francesco Colombo, Gloria Goi, Pietro Zerbi, Barbara Pirrò, Piergiorgio Danelli
    Frontiers in Surgery.2022;[Epub]     CrossRef
  • Adult intussusception: a challenge to laparoscopic surgery?
    Mingze Sun, Zhongmin Li, Zhenbo Shu, Qi Wu, Xue Liu
    PeerJ.2022; 10: e14495.     CrossRef
  • Adult Jejuno-jejunal intussusception due to inflammatory fibroid polyp
    Yi-Kai Kao, Jian-Han Chen
    Medicine.2020; 99(36): e22080.     CrossRef
Case Reports
Adult intussusception caused by inverted Meckel's diverticulum treated with operation.
Sung Yun Lee, Jae Yoon Jeong, Seung Hyun Hong, Seung Min Woo, Su Heui Lee, Hyun Joo You, Dong Won Kim
Yeungnam Univ J Med. 2016;33(2):116-119.   Published online December 31, 2016
DOI: https://doi.org/10.12701/yujm.2016.33.2.116
  • 2,204 View
  • 10 Download
AbstractAbstract PDF
Intussusception is a serious disease where part of the intestine slides into an adjacent part of the intestine. Adult intussusception is mainly due to benign or malignant neoplasm. Therefore, in most cases of adult intussusception, treatment by surgery would be preferable to conservative therapy. However, we report on a 28-year-old female patient who underwent intussusception operation delayed 3 months. Abdominal computed tomography 3 months ago showed a small bowel intussusception measuring 20 cm long. Three months later, the previously identified small bowel intussusception appeared without change. The patient underwent surgery, and ectopic gastric mucosa was observed in the biopsy. Therefore, Meckel's diverticulum was diagnosed.
A Case of Eosinophilic Bronchitis Associated with Tracheal Diverticulum.
Seung Hoon Yoo, Jae Ho Chung, Byung Soo Kang, Won Sik Kang, Won Jun Koh, Min Kyung Lee, Chan Sub Park
Yeungnam Univ J Med. 2011;28(2):192-195.   Published online December 31, 2011
DOI: https://doi.org/10.12701/yujm.2011.28.2.192
  • 1,838 View
  • 1 Download
AbstractAbstract PDF
Tracheal diverticulum is relatively rare. It results from congenital or acquired weakness of the tracheal wall. Most cases are asymptomatic, but when symptoms are present, they are usually nonspecific. A 54-year-old man complained of sputum lasting for several months. Chest computed tomography showed an air-containing cystic structure in the trachea. Fiberoptic bronchoscopy demonstrated ostium arising from the right posterolateral wall at the trachea. Reported herein is a case of eosinophilic bronchitis associated with tracheal diverticulum.
2 cases of male urethral diverticulum combined with stone.
Hyun Chul Shin, Young Soo Kim, Tong Choon Park
Yeungnam Univ J Med. 1992;9(2):416-421.   Published online December 31, 1992
DOI: https://doi.org/10.12701/yujm.1992.9.2.416
  • 1,588 View
  • 2 Download
AbstractAbstract PDF
Male urethral diverticulum is uncommon lesion, furthermore calculus formation within the male urethral diverticulum is very rare. Generally, urethral diverticula are classified as congenital and acquired. The majority of male urethral diverticula are acquired and approximately 10 to 20 per cent are congenital. Acquired urethral diverticula in the male may arise from many sources, including infection (prostatic abscess, infection of periurethral glands, hematoma or schistosomiasis), obstruction (stricture, impacted stone, Cunningham clamp or condom catheter) and trauma (instrumentation, external injury and pelvic fracture). Calculi formation is more common in the acquired diverticulum owing to stagnation of urine and infection. These calculi in the diverticulum usually are solitary and may attain considerable size with predisposing factors, 1) a ureteral or bladder calculus that is lodged in the urethra 2) urethral trauma or stricture, 3) calcification around a foreign body or hair. The treatment of urethral diverticulum combined with stone is excision of the diverticula with removal of stone. We treated two cases of urethral diverticulum combined with stone in the male, and report with review of literature.
Congenital Left Ventricular Diverticulum.
Jong Young Kim, Jung Ho Kim, Jin Gon Jun
Yeungnam Univ J Med. 1990;7(2):181-187.   Published online December 31, 1990
DOI: https://doi.org/10.12701/yujm.1990.7.2.181
  • 1,659 View
  • 1 Download
AbstractAbstract PDF
Congenital diverticulosis of the left ventricle is an extremely are rare maldevelopment. We report a 9 year old girl with probable isolated left ventricular diverticulum in whom the diagnosis was made by cross sectional echocardiography and by angiography.

JYMS : Journal of Yeungnam Medical Science
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