scholarly journals An adult case of a retroperitoneal isolated enteric duplication cyst with the imaging changes over time

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Mayu Inomata ◽  
Kengo Kai ◽  
Takuto Ikeda ◽  
Akiko Ichihara ◽  
Rie Masuda ◽  
...  

Abstract Background Adult cases of retroperitoneal isolated enteric duplication cyst (IEDC) are rare, with only 17 case reports in the relevant literature. We herein present a case, which was characterized by changes in intra-cystic density on computed tomography (CT), which was safely resected by laparoscopic surgery. Case presentation The patient was a 60-year-old male who received abdominal CT to investigate the cause of increased serum CA19-9 levels. CT revealed a unilocular cystic mass located in the lower right retroperitoneum. The size increased from 5 to 10 cm in three and a half years and the CT value decreased from 101 Hounsfield Units (HU) to 20 HU. We performed laparoscopic surgical resection, because the possibility that the enlargement of the lesion represented malignant transformation could not be denied. The large cystic mass firmly adhered to the appendix and its mesentery via the retroperitoneum, the appendix was resected en bloc with the cystic lesion. Microscopically, it had no communication with the appendix, and had an intestinal wall structure of muscularis mucosae and muscularis propria. The final pathological diagnosis was IEDC in the retroperitoneal space. There was no histological evidence of malignancy. Conclusion When we encounter a retroperitoneal cystic lesion, we should consider the possibility of malignancy to determine the treatment strategy and perform a careful operation without breaking the cyst wall, irrespective of the preoperative diagnosis.

2020 ◽  
pp. 1-1
Author(s):  
Priyanka Pant ◽  
Samindra Nath Basak

A 16 year old adolescent boy with painless abdominal distension. Computed Tomography showed large multiloculated abdomino pelvic cystic lesion compressing adjacent structures without any communication to the stomach, pancreas, small and large gut.


2013 ◽  
Vol 18 (5) ◽  
pp. 1054-1058 ◽  
Author(s):  
Alexander S. Chiu ◽  
David Bluhm ◽  
Shu-Yan Xiao ◽  
Irving Waxman ◽  
Jeffrey B. Matthews

2019 ◽  
Vol 54 ◽  
pp. 83-86
Author(s):  
Shinsuke Nakashima ◽  
Terumasa Yamada ◽  
Go Sato ◽  
Takaaki Sakai ◽  
Yoshinao Chinen ◽  
...  

1983 ◽  
Vol 76 (5) ◽  
pp. 670-671 ◽  
Author(s):  
PATRICIA YOUNGBLOOD ◽  
BERNARD I. BLUMENTHAL

2020 ◽  
Vol 05 (02) ◽  
pp. 73-76
Author(s):  
Shubha H V ◽  
Archana Shetty ◽  
Vijaya C ◽  
Venkatachalapathy V

2017 ◽  
Vol 2017 ◽  
pp. 1-4 ◽  
Author(s):  
Shigeo Iijima

Enteric duplication cysts are rare congenital anomalies that are prenatally diagnosed through antenatal ultrasonography (US). In female patients, however, attention must be paid since these formations might be confused with ovarian cysts. Herein, we present a case of a low birth weight female infant with an enteric duplication cyst. A cystic lesion was detected in the right abdomen of the fetus on antenatal US and magnetic resonance imaging (MRI). Serial US and MRI examinations performed after birth showed a single cyst that wandered from side to side in the abdomen; the initial diagnosis was thought to be an ovarian cyst. During laparotomy, however, it was found to be an enteric duplication cyst with volvulus. To our knowledge, there has been no report of an enteric duplication cyst presenting as a wandering abdominal mass. Our experience indicates that early intervention is necessary for patients who have a wandering abdominal mass to avoid complications and urgent surgery, whether it is an ovarian cyst or an enteric duplication cyst.


2004 ◽  
Vol 24 (2) ◽  
pp. 98-100 ◽  
Author(s):  
Thierry Rousseau ◽  
Stéphanie Couvreur ◽  
Eve Senet-Lacombe ◽  
Christine Durand ◽  
Eve Justrabo ◽  
...  

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Murphy R. Mastin ◽  
Leah A. Swanson ◽  
Thomas C. Smyrk ◽  
Carilyn N. Wieland ◽  
Ruifeng Guo

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