scholarly journals Laparoscopic resection of a peritoneal inclusion cyst mimicking an ovarian borderline tumor

Author(s):  
Michihide Maeda ◽  
Hikari Unno ◽  
Yukako Oi ◽  
Sahori Kakuda ◽  
Masahiro Watanabe ◽  
...  
Author(s):  
Payam Katebi Kashi ◽  
George W. Stone ◽  
G. Scott Rose ◽  
Jeffrey A. Welgoss ◽  
Katherine L. Dengle

2011 ◽  
Vol 27 (5) ◽  
pp. 430-431 ◽  
Author(s):  
Victor Ho-Fung ◽  
Camilo E. Jaimes ◽  
Avrum N. Pollock

2019 ◽  
Vol 2019 ◽  
pp. 1-5
Author(s):  
Yoko Fujimoto ◽  
Hironori Takahashi ◽  
Kenji Horie ◽  
Takeo Nakaya ◽  
Toshiro Niki ◽  
...  

We describe a patient with bilateral cystic tumors of the pelvis. The left one rapidly grew during pregnancy and combined with the right one, whose clinical course made diagnosis difficult. A pregnant woman with a history of laparotomy was referred to us due to suspected bilateral pelvic cysts. The left-sided cyst had rapidly grown to 27 cm in diameter and merged with the right cyst, forming a large cyst occupying the entire pelvic cavity in the third trimester. Considering this rapid growth, cesarean section and resection of the cyst were performed at 37th week. The resected cyst consisted of two components: a large unilocular cyst containing serous fluid and a multilocular cyst suggestive of ovarian mucinous cystadenoma in the right ovary. The wall of the former largely lacked lining epithelium, but it was partly continuous with the latter mucinous epithelium. Immunohistochemically, estrogen and progesterone receptors were focally positive in the cyst wall, suggesting that pregnancy-associated sex-hormones may have contributed to the rapid growth of the cyst. We diagnosed this condition as a peritoneal inclusion cyst margining with a right ovarian mucinous cystadenoma. Peritoneal inclusion cyst should be considered in the differential diagnosis of a rapidly growing pelvic mass during pregnancy.


2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Jianjun Xu ◽  
Shaobo Hu ◽  
Suzhen Li ◽  
Weimin Wang ◽  
Xing Zhou ◽  
...  

Abstract Background Hepatic epithelioid hemangioendothelioma (HEHE) is an extremely rare borderline tumor of vascular endothelial origin. Laparoscopic resection of HEHE has never been reported. Methods The clinical data of eleven patients with HEHE (4 women and 7 men) who were diagnosed and treated at the Union Hospital (Wuhan, China), and Wuhan Asia General Hospital (Wuhan, China), between March 2012 and July 2020 were analyzed retrospectively. Results The mean age of HEHE patients was 42.4 ± 13.9 years (range 22–67 years). All patients underwent laparoscopic surgery alone or in combination with radiofrequency ablation. Most tumors showed aggressive growth or metastasis. By immunohistochemistry, tumor cells were positive for CD31, CD34, ERG, PCK, FLi-1, TFE-3, and Ki-67 (labeling index range, 5–15%). In one of the patients, the tumor was accompanied by partial necrosis with a local appearance of epithelioid angiosarcoma. Postoperative adjuvant treatment included chemotherapy, sorafenib, and Huaier granule. As of July 2020, the median follow-up duration was 36 months (range, 9–60 months), with 2 (18.2%) patients experiencing tumor recurrence. Conclusions This is the first report of laparoscopic hepatectomy of HEHE. Curative laparoscopic hepatectomy might be an acceptable treatment for appropriate HEHE patients.


2012 ◽  
Vol 40 (1) ◽  
pp. 51-55 ◽  
Author(s):  
Tomonobu Kanasugi ◽  
Akihiko Kikuchi ◽  
Hideo Omi ◽  
Maki Ikeda ◽  
Akimune Fukushima ◽  
...  

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