Duodenal duplication cyst in an adult: a rare case.
Duodenal duplication cysts are rare congenital anomalies, found commonly in infants and children. In rare instances they can occur in adults, often manifesting clinically as pancreatitis. We here present one such case of an 18-year-old female, who presented with symptoms of duodenal obstruction, wei...
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Department of Surgery, UKM Medical Centre
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oai:generic.eprints.org:77002016-12-14T06:44:55Z http://journalarticle.ukm.my/7700/ Duodenal duplication cyst in an adult: a rare case. Raghunath P, Neha K, Sakshi S, Rajgopal S, Kuladeepa AV, Duodenal duplication cysts are rare congenital anomalies, found commonly in infants and children. In rare instances they can occur in adults, often manifesting clinically as pancreatitis. We here present one such case of an 18-year-old female, who presented with symptoms of duodenal obstruction, weight loss and pancreatitis. She was diagnosed as having a duodenal duplication cyst (DDC) on a CT scan. She made a good recovery after a total cyst excision. This case report aims to highlight the importance of clinicians having duplication cysts in their list of differential diagnoses as these cases are often under-diagnosed due to their rare occurrences. Department of Surgery, UKM Medical Centre 2014-01-01 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/7700/1/13._MS1159_%2857-59%29.pdf application/pdf en http://journalarticle.ukm.my/7700/2/ Raghunath P, and Neha K, and Sakshi S, and Rajgopal S, and Kuladeepa AV, (2014) Duodenal duplication cyst in an adult: a rare case. Journal of Surgical Academia, 4 (1). pp. 57-59. ISSN 2231-7481 http://jsurgacad.com/ |
repository_type |
Digital Repository |
institution_category |
Local University |
institution |
Universiti Kebangasaan Malaysia |
building |
UKM Institutional Repository |
collection |
Online Access |
language |
English English |
description |
Duodenal duplication cysts are rare congenital anomalies, found commonly in infants and children. In rare instances they can occur in adults, often manifesting clinically as pancreatitis. We here present one such case of an 18-year-old female, who presented with symptoms of duodenal obstruction, weight loss and pancreatitis. She was diagnosed as having a duodenal duplication cyst (DDC) on a CT scan. She made a good recovery after a total cyst excision. This case report aims to highlight the importance of clinicians having duplication cysts in their list of differential diagnoses as these cases are often under-diagnosed due to their rare occurrences. |
format |
Article |
author |
Raghunath P, Neha K, Sakshi S, Rajgopal S, Kuladeepa AV, |
spellingShingle |
Raghunath P, Neha K, Sakshi S, Rajgopal S, Kuladeepa AV, Duodenal duplication cyst in an adult: a rare case. |
author_facet |
Raghunath P, Neha K, Sakshi S, Rajgopal S, Kuladeepa AV, |
author_sort |
Raghunath P, |
title |
Duodenal duplication cyst in an adult: a rare case. |
title_short |
Duodenal duplication cyst in an adult: a rare case. |
title_full |
Duodenal duplication cyst in an adult: a rare case. |
title_fullStr |
Duodenal duplication cyst in an adult: a rare case. |
title_full_unstemmed |
Duodenal duplication cyst in an adult: a rare case. |
title_sort |
duodenal duplication cyst in an adult: a rare case. |
publisher |
Department of Surgery, UKM Medical Centre |
publishDate |
2014 |
url |
http://journalarticle.ukm.my/7700/ http://journalarticle.ukm.my/7700/ http://journalarticle.ukm.my/7700/1/13._MS1159_%2857-59%29.pdf http://journalarticle.ukm.my/7700/2/ |
first_indexed |
2018-09-07T10:05:22Z |
last_indexed |
2018-09-07T10:05:22Z |
_version_ |
1610942746753761280 |