scholarly journals Co-existence of acute appendicitis and inflammatory myofibroblastic tumor of the small intestine: A case report

2015 ◽  
Vol 4 (3) ◽  
pp. 217-220 ◽  
Author(s):  
Nurcan Unver ◽  
Ganime Coban ◽  
Oyku Izel Onaran ◽  
Enver Kunduz ◽  
Adnan Arslan ◽  
...  
2016 ◽  
Vol 10 (1) ◽  
Author(s):  
Alexandra Oeconomopoulou ◽  
Yvelise de Verney ◽  
Katerina Kanavaki ◽  
Kalliopi Stefanaki ◽  
Kitty Pavlakis ◽  
...  

2010 ◽  
Vol 67 (12) ◽  
pp. 1021-1024 ◽  
Author(s):  
Snezana Pavlovic ◽  
Dejan Janjic ◽  
Suncica Mihajlovic ◽  
Natalija Stefanovic ◽  
Miljana Pavlovic ◽  
...  

Background. Meckel?s diverticulum (MD) is a congenital anomaly of the small intestine. It results from incomplete obliteration and resorption of the proximal omphaloenteric duct connecting yolk sac with primitive gut in the fetal period. Case report. A case of 20-year old female with ectopic pancreatic rests in a MD was reported. She was hospitalized with clinical signs of acute appendicitis. During surgery an inflamated Meckel?s diverticulum was found and a clinoid resection of the diverticulum was performed. Histologic examination revealed pancreatic tissue in the removed diverticulum. Endocrine cells (EC) were detected with Masson staining and aberrant pancreatic tissue with immunocytochemical LSAB2 method using pan cytokeratin as epithelial marker. Conclusion. Most of MD are asymptomatic and accessory finding during laparothomias for different causes, but complications of undiagnozed MD can be serious (diverticulitis, perforation with peritonitis or intestinal obstruction caused by invagination). In unclear cases, additional cytochemical and immunocytochemical diagnostics could be done.


F1000Research ◽  
2017 ◽  
Vol 6 ◽  
pp. 677
Author(s):  
Julie Leganger ◽  
Rikke Raagaard Soerensen ◽  
Jacob Rosenberg ◽  
Jakob Burcharth

Introduction: Inflammatory myofibroblastic tumors (IMTs) are uncommon mesenchymal lesions classified by WHO as neoplasms of uncertain behavior. Morphologically, IMTs are composed of proliferating spindled myofibroblastic cells accompanied by a marked - usually chronic - inflammatory infiltrate. The etiology is unknown, but several theories have been suggested, including an association with Wilms’ tumor. IMTs are rarely diagnosed in adults and have been reported in various organs. IMTs are considered benign but with a potential to recur at their primary site. Case report: A 44-year-old female experienced intermittent severe abdominal pain, loose stools and a visible abdominal bulge. In early childhood the patient had been treated for a Wilms’ tumor. At admission Meckel’s diverticulitis was suspected, but during surgery a tumor in the terminal ileum, creating a conglomerate of small intestinal loops, was observed and completely resected.  The pathology report characterized the tumor as a histologically benign inflammatory myofibroblastic tumor. Postoperatively, the patient experienced several complications including an anastomotic leakage and subsequent formation of an abscess and transcutaneous fistula. Discussion: IMTs rarely arise in the small intestine, and to our knowledge the manifestation of a small intestine conglomerate has not been described previously. Making the diagnosis is difficult, and numerous differential diagnoses were possible in this case. Approximately 8-25% of IMTs in the gastrointestinal tract recur locally. Complete surgical resection is the treatment of choice, and re-excision is the preferred therapy for local recurrence.  To our knowledge, no guidelines concerning follow-ups are available. Conclusion: IMTs in the terminal ileum can mimic Meckel’s diverticulitis and present with symptoms of obstructive ileus due to the formation of a conglomerate of small intestinal loops. Furthermore, IMTs should be considered as a diagnostic possibility in patients with a past medical history of Wilms’ tumor.


2020 ◽  
Vol 56 ◽  
pp. 101423
Author(s):  
Rina Harada ◽  
Masahiro Ohtaki ◽  
Naoki Hashizume ◽  
Akihiro Takeshi ◽  
Eishiro Murai ◽  
...  

2016 ◽  
Vol 22 ◽  
pp. 44-46 ◽  
Author(s):  
Abdolhamid Amouei ◽  
Fatemeh Ehsani ◽  
Marzie Vaghefi ◽  
Seyed Mostafa Tabatabai ◽  
Pouria Yazdian Anari

F1000Research ◽  
2017 ◽  
Vol 6 ◽  
pp. 677
Author(s):  
Julie Leganger ◽  
Rikke Raagaard Soerensen ◽  
Jacob Rosenberg ◽  
Jakob Burcharth

Introduction: Inflammatory myofibroblastic tumors (IMTs) are uncommon mesenchymal lesions classified by WHO as neoplasms of uncertain behavior. Morphologically, IMTs are composed of proliferating spindled myofibroblastic cells accompanied by a marked - usually chronic - inflammatory infiltrate. The etiology is unknown, but several theories have been suggested, including an association with Wilms’ tumor. IMTs are rarely diagnosed in adults and have been reported in various organs. IMTs are considered benign but with a potential to recur at their primary site. Case report: A 44-year-old female experienced intermittent severe abdominal pain, loose stools and a visible abdominal bulge. In early childhood the patient had been treated for a Wilms’ tumor. At admission Meckel’s diverticulitis was suspected, but during surgery a tumor in the terminal ileum, creating a conglomerate of small intestinal loops, was observed and completely resected.  The pathology report characterized the tumor as a histologically benign inflammatory myofibroblastic tumor. Postoperatively, the patient experienced several complications including an anastomotic leakage and subsequent formation of an abscess and transcutaneous fistula. Discussion: IMTs rarely arise in the small intestine, and to our knowledge the manifestation of a small intestine conglomerate has not been described previously. Making the diagnosis is difficult, and numerous differential diagnoses were possible in this case. Approximately 8-25% of IMTs in the gastrointestinal tract recur locally. Complete surgical resection is the treatment of choice, and re-excision is the preferred therapy for local recurrence.  To our knowledge, no guidelines concerning follow-ups are available. Conclusion: IMTs in the terminal ileum can mimic Meckel’s diverticulitis and present with symptoms of obstructive ileus due to the formation of a conglomerate of small intestinal loops. Furthermore, IMTs should be considered as a diagnostic possibility in patients with a past medical history of Wilms’ tumor.


2001 ◽  
Vol 45 (4) ◽  
pp. 417
Author(s):  
Jong Myeong Yang ◽  
Kyu Soon Kim ◽  
Soon Tae Kwon ◽  
Jong Chul Kim ◽  
Kyu Sang Song

Kanzo ◽  
2012 ◽  
Vol 53 (5) ◽  
pp. 272-277 ◽  
Author(s):  
Hisashi Kosaka ◽  
Nobukazu Kuroda ◽  
Norihiro Nakai ◽  
Koichiro Ohashi ◽  
Kazuhiro Suzumura ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Zhicheng Zhang ◽  
Xiaowei Huang ◽  
Qian Chen ◽  
Demin Li ◽  
Qi Zhou ◽  
...  

Abstract Background Small intestine duplication cysts (SIDCs) are rare congenital anatomical abnormalities of the digestive tract and a rare cause of hematochezia. Case presentation We describe an adult female presented with recurrent hematochezia. The routine gastric endoscope and colonic endoscope showed no positive findings. Abdominal CT scan indicated intussusception due to the "doughnut" sign, but the patient had no typical symptoms. Two subsequent capsule endoscopes revealed a protruding lesion with bleeding in the distal ileum. Surgical resection was performed and revealed a case of SIDC measuring 6 * 2 cm located inside the ileum cavity. The patient remained symptom-free throughout a 7-year follow-up period. Conclusion SIDCs located inside the enteric cavity can easily be misdiagnosed as intussusception by routine radiologic examinations.


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