scholarly journals Primary amyloidosis involving the gastrointestinal tract, mesentery and omentum: A case report

2021 ◽  
Vol 22 (4) ◽  
Author(s):  
Guihua Duan ◽  
Min Qi ◽  
Qiang Guo ◽  
Zhengji Song
2015 ◽  
Vol 24 (2) ◽  
pp. 235-239 ◽  
Author(s):  
Jan Ulrych ◽  
Vladimir Fryba ◽  
Helena Skalova ◽  
Zdenek Krska ◽  
Tomas Krechler ◽  
...  

Heterotopic pancreas is a congenital pathology of the gastrointestinal tract, particularly rare in the esophagus. Both symptomatology and findings during preoperative examinations are non-specific and therefore do not often lead to an accurate diagnosis, which is usually revealed only by histopathological assessment of a resected specimen. We report an unusual case of a patient suffering from severe dysphagia caused by heterotopic pancreas in the distal esophagus with chronic inflammation and foci of premalignant changes. This article also reviews 14 adult cases of heterotopic pancreas in the esophagus previously reported in the literature, with the aim of determining the clinical features of this disease and possible complications including rare premalignant lesions and malignant transformation. Especially with regard to those complications, we suggest that both symptomatic and incidentally found asymptomatic lesions should be resected.


2021 ◽  
Author(s):  
Bahareh Ebrahimi ◽  
Seyed Vahid Hosseini ◽  
Neda Haghighat ◽  
Nader Moeinvaziri ◽  
Masoud Amini ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Faruk Karateke ◽  
Ebru Menekşe ◽  
Koray Das ◽  
Sefa Ozyazici ◽  
Pelin Demirtürk

Crohn's disease may affect any segment of the gastrointestinal tract; however, isolated duodenal involvement is rather rare. It still remains a complex clinical entity with a controversial management of the disease. Initially, patients with duodenal Crohn' s disease (DCD) are managed with a combination of antiacid and immunosuppressive therapy. However, medical treatment fails in the majority of DCD patients, and surgical intervention is required in case of complicated disease. Options for surgical management of complicated DCD include bypass, resection, or stricturoplasty procedures. In this paper, we reported a 33-year-old male patient, who was diagnosed with isolated duodenal Crohn’s diseases, and reviewed the surgical options in the literature.


2006 ◽  
Vol 130 (2) ◽  
pp. 201-204 ◽  
Author(s):  
Payal Kapur ◽  
Dinesh Rakheja ◽  
Michael Bastasch ◽  
Kyle H. Molberg ◽  
Venetia R. Sarode

Abstract Primary thymic mucinous adenocarcinoma is extremely rare; to our knowledge, only 2 cases have been reported to date. We describe a third case of primary mucinous adenocarcinoma of the thymus in a 41-year-old man who presented with an anterior mediastinal mass with subsequent metastasis to the lung. The initial diagnosis was of metastatic mucinous adenocarcinoma, but extensive clinical workup of the patient failed to reveal a primary tumor elsewhere in the body. The specific identification of mucinous adenocarcinoma as a primary thymic neoplasm can be difficult or impossible. Morphologic and immunophenotypic similarities to mucinous adenocarcinomas of the gastrointestinal tract can pose diagnostic challenges for surgical pathologists, especially in small biopsy specimens.


Author(s):  
Fareeha Farooqui ◽  
Sehrish Latif ◽  
Humera Naz Altaf ◽  
Sania Waseem ◽  
Sohaib Khan ◽  
...  

Abstract Mucinous cystadenoma is a rare tumor of appendix it accounts for only 0.4% of the gastrointestinal tract malignancies and is reported rarely in literature. Therefore the surgical management is not yet established. Here we report a case of a 65 year old female who presented with a dragging sensation and a feeling of mass in right iliac fossa. Her computed tomography (CT) suggested an abscess formation of the parietal peritoneum. She was planned for laparotomy and upon exploration a mass was found arising from tip of retroperitoneal appendix. Whole of the appendix was studded with mucoid material. Limited right hemicolectomy was performed and histopathology of appendix showed mucinous cystadenoma with no evidence of malignant changes. Patient remained uneventful and was discharged on 4th post operative day. The unusual presentation of retroperitoneal pseudomyxoma without any intraperitoneal pathology, prompted us to report this case. Continuous...


2016 ◽  
Vol 38 (2) ◽  
Author(s):  
Marco Gasparella ◽  
Maurizio Marzaro ◽  
Mario Ferro ◽  
Carlo Benetton ◽  
Vittorina Ghirardo ◽  
...  

Meckel’s diverticulum is a common anomaly of the gastrointestinal tract. The most common complications of Meckel’s diverticulum are inflammation, bleeding and obstruction. We present a 12-year-old boy with bowel obstruction due to phytobezoar in a Meckel’s diverticulum. We describe diagnostic difficulties and our surgery approach comparing it to the literature.


2017 ◽  
Vol 45 (12) ◽  
pp. 1137-1141 ◽  
Author(s):  
Takashi Kato ◽  
Shin Ichihara ◽  
Hiroko Gotoda ◽  
Shunji Muraoka ◽  
Terufumi Kubo ◽  
...  

1991 ◽  
Vol 30 (6) ◽  
pp. 597-599 ◽  
Author(s):  
Toshio ITOH ◽  
Shinichiro OHASHI ◽  
Takeshi TSUJINO ◽  
Mutsumi TAKENAKA ◽  
Hitoshi KODAMA ◽  
...  

2015 ◽  
Vol 9 (1) ◽  
Author(s):  
Woo-Ram Moon ◽  
Do-Sik Moon ◽  
JoA Kim ◽  
Young-min Yoon ◽  
Byung-Seok Choi ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document