scholarly journals A CASE OF BRUNNERS GLAND HAMARTOMA CAUSING OBSTRUCTIVE JAUNDICE

2020 ◽  
pp. 41-42
Author(s):  
Unnati Shah

Brunner’s gland hamartoma is a rare benign tumor of duodenum .We present a case of large pedunculated duodenal hamartoma causing obstructive jaundice and significant dilatation of intrahepatic biliary radicles. Duodenal polyp is a rare benign tumor formed from a proliferation of Brunner gland, typically forming polypoid growth in proximal duodenum and can extend up to 3rd part of duodenum. It may be incidental finding but can present in emergency with obstruction and hemorrhage requiring surgical endoscopic resection.

2020 ◽  
Vol 15 (1) ◽  
pp. 237-240
Author(s):  
Bo Yang ◽  
Ke Li ◽  
Runlan Luo ◽  
Zuming Xiong ◽  
Lianwei Wang ◽  
...  

AbstractBackgroundBrunner’s gland adenoma is a rare benign tumor arising from Brunner’s glands. It is mostly small in size, and patients with this tumor are asymptomatic.Case presentationWe report the case of a 63-year-old woman with upper gastrointestinal obstruction for almost 10 years, who was pathologically diagnosed with large Brunner’s gland adenoma of the duodenum. Postoperatively, no sign of recurrence has been noted until now.ConclusionThis study may help clinicians to understand and provide a more accurate diagnosis of Brunner’s gland adenoma.


2020 ◽  
Vol 10 (2) ◽  
Author(s):  
Lubna Kamani ◽  
Ravi Raj ◽  
Rabia Ali ◽  
Faisal Siddiqi

Brunner’s gland hyperplasia (BGH) is an unusual entity that presents with large duodenal polyp or mass and rarely causes gastrointestinal bleeding. It is usually asymptomatic and often an incidental finding during the esophagoduodenoscopy (EGD). However, most of the cases are benign. We encounter a 40 years old man who presented in Emergency Room with melena. EGD revealed solitary, large duodenal polyp in second part of duodenum and later histopathological findings were consistent with BGH.


2006 ◽  
Vol 72 (7) ◽  
pp. 649-654 ◽  
Author(s):  
Vijaykumar G. Patel ◽  
Olufemi A. Babalola ◽  
James K. Fortson ◽  
William L. Weaver

Adrenal myelolipoma is a rare benign tumor composed of mature lipomatous and hemopoietic tissue. Although it is often discovered as an incidental finding on imaging of the abdomen for some other reason or at autopsy, adrenal myelolipoma has been reported to present with symptoms such as flank pain resulting from tumor bulk, necrosis, or spontaneous retroperitoneal hemorrhage. Myelolipomas are hormonally inactive but have also been reported to coexist with other hormonally active tumors of the adrenal gland. They are usually unilateral but may be bilateral and may also develop in extraadrenal sites like the retroperitoneum, thorax, and pelvis. We report a patient with symptomatic adrenal myelolipoma diagnosed on computed tomography scan and confirmed on computed tomography-guided biopsy. The patient underwent surgical resection for symptomatic relief. We also review the literature to evaluate the presentation and optimal management of this rare adrenal tumor that is not encountered by most general surgeons and therefore not well known to most surgeons.


Endoscopy ◽  
2014 ◽  
Vol 46 (S 01) ◽  
pp. E310-E311
Author(s):  
Lucia Sparano ◽  
Pietro Cesari ◽  
Mauro Lovera ◽  
Fausto Zorzi ◽  
Alessandro Paterlini

2008 ◽  
Vol 32 (1) ◽  
pp. 11-14 ◽  
Author(s):  
R. Coriat ◽  
M. Mozer-Bernardeau ◽  
B. Terris ◽  
A. Chryssostalis ◽  
F. Prat ◽  
...  

2000 ◽  
Vol 52 (3) ◽  
pp. 435-436 ◽  
Author(s):  
Eliahu Shemesh ◽  
Shomron Ben Horin ◽  
Iris Barshack ◽  
Simon Bar-Meir

2020 ◽  
Vol 97 (1) ◽  
pp. 103-105
Author(s):  
Kodai Esaki ◽  
Yasusato Matsuda ◽  
Yuki Sugawara ◽  
Shinji Ono ◽  
Hiroaki Onoyama ◽  
...  

2012 ◽  
Vol 75 (4) ◽  
pp. AB250-AB251
Author(s):  
Mingyan Cai ◽  
Ping-Hong Zhou ◽  
Liqing Yao

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