| _version_ | 1866901635138060288 |
|---|---|
| author | Afreen Munir*, Arun pandian, Haja Sherief Sheik, T. Sivakumar |
| author_facet | Afreen Munir*, Arun pandian, Haja Sherief Sheik, T. Sivakumar |
| contents | <div> <p><strong><span>Abstract: </span></strong></p> <p><em><span>Wilkie's syndrome is an uncommon condition resulting from the superior mesenteric artery (SMA) at its origin exerting extrinsic compression on the duodenum's third segment. The non-specific and fluctuating symptoms include postprandial symptoms include weight loss, anorexia, early satiety, nausea, vomiting, and stomach pain.</span></em></p> <p><strong><em><span>Objectives:</span></em></strong><em><span> To aware diagnose and manage a rare case of Wilkie's Syndrome</span></em></p> <p><strong><em><span>Methodology:</span></em></strong><em><span> We brought in a female patient, 29 years old who previously experienced bilious vomiting, nausea, and cramping and pain in her abdomen. She had experienced a similar ailment for the previous year.Initial results fromUGD scanning reveal a duodenal air bubble.Duodenoscopy,which display the third and fourth segments of the duodenum dilated.UGD scanning reveal a duodenal air bubble. Duedenoscopy, which displays the third and fourth segments of duodenum dilated. No evidence of a lesion in the first or second portion of duodenum is seen on an upper GI scopy. Stomach was found to be normal, ruling out GERD. Following a laparoscopic (roux en y) Duodenojejunostomy, the patient's intraoperative results were in line with the diagnosis. <br>There were no complications during the surgery or the recovery period, and the patient was released on the sixth day following surgery.</span></em></p> <p><strong><em><span>Conclusion: </span></em></strong><em><span>Wilkie's Syndrome is an uncommon illness. There have only been 500 cases worldwide to date. In long-term instances, surgery is the preferred course of treatment because non-surgical methods run the risk of deadly consequences such as severe malnourishment, imbalanced electrolytes, gastric rupture, spontaneous upper gastrointestinal bleeding, or abrupt cardiac collapse.</span></em></p> <p><strong><em><span>Keywords: Wilkie’s </span></em></strong><span><em><span>syndrome, post-prandial abdominal pain, Roun en Y duodenojejunostomy, intestinal obstruction, superior mesenteric artery syndrome</span></em></span></p> </div> |
| format | Recurso digital |
| id | zenodo_https___doi_org_10_5281_zenodo_13947856 |
| institution | Zenodo |
| language | |
| publishDate | 2024 |
| publisher | Zenodo |
| record_format | zenodo |
| spellingShingle | SUPERIOR MESENTERIC ARTERY SYNDROME/ WILKIE SYNDROME –A CASE REPORT Afreen Munir*, Arun pandian, Haja Sherief Sheik, T. Sivakumar <div> <p><strong><span>Abstract: </span></strong></p> <p><em><span>Wilkie's syndrome is an uncommon condition resulting from the superior mesenteric artery (SMA) at its origin exerting extrinsic compression on the duodenum's third segment. The non-specific and fluctuating symptoms include postprandial symptoms include weight loss, anorexia, early satiety, nausea, vomiting, and stomach pain.</span></em></p> <p><strong><em><span>Objectives:</span></em></strong><em><span> To aware diagnose and manage a rare case of Wilkie's Syndrome</span></em></p> <p><strong><em><span>Methodology:</span></em></strong><em><span> We brought in a female patient, 29 years old who previously experienced bilious vomiting, nausea, and cramping and pain in her abdomen. She had experienced a similar ailment for the previous year.Initial results fromUGD scanning reveal a duodenal air bubble.Duodenoscopy,which display the third and fourth segments of the duodenum dilated.UGD scanning reveal a duodenal air bubble. Duedenoscopy, which displays the third and fourth segments of duodenum dilated. No evidence of a lesion in the first or second portion of duodenum is seen on an upper GI scopy. Stomach was found to be normal, ruling out GERD. Following a laparoscopic (roux en y) Duodenojejunostomy, the patient's intraoperative results were in line with the diagnosis. <br>There were no complications during the surgery or the recovery period, and the patient was released on the sixth day following surgery.</span></em></p> <p><strong><em><span>Conclusion: </span></em></strong><em><span>Wilkie's Syndrome is an uncommon illness. There have only been 500 cases worldwide to date. In long-term instances, surgery is the preferred course of treatment because non-surgical methods run the risk of deadly consequences such as severe malnourishment, imbalanced electrolytes, gastric rupture, spontaneous upper gastrointestinal bleeding, or abrupt cardiac collapse.</span></em></p> <p><strong><em><span>Keywords: Wilkie’s </span></em></strong><span><em><span>syndrome, post-prandial abdominal pain, Roun en Y duodenojejunostomy, intestinal obstruction, superior mesenteric artery syndrome</span></em></span></p> </div> |
| title | SUPERIOR MESENTERIC ARTERY SYNDROME/ WILKIE SYNDROME –A CASE REPORT |
| url | https://doi.org/10.5281/zenodo.13947856 |