Multilocular peritoneal inclusion cyst with extensive xanthogranulomatous stromal changes: A differential diagnosis of cystic pelvic tumors in women

2000 ◽  
Vol 4 (5) ◽  
pp. 308-310 ◽  
Author(s):  
Hermann Brustmann
Author(s):  
Payam Katebi Kashi ◽  
George W. Stone ◽  
G. Scott Rose ◽  
Jeffrey A. Welgoss ◽  
Katherine L. Dengle

2020 ◽  
Vol 13 (4) ◽  
pp. 369-383
Author(s):  
Ju. V. Nosova ◽  
A. E. Solopova ◽  
G. N. Khabas ◽  
A. V. Asaturova

Introduction. Most pelvic tumors originate from reproductive organs. Even using the up-to-date imaging techniques, radiologists experience difficulties in determining the source of the lesion since a wide range of tumors look similar to each other on the distorted backdrop of pelvic anatomy, large invasive formations, and an active inflammatory reaction of the pelvic peritoneum.Aim: to evaluate “pitfalls” in the preoperative noninvasive diagnosis of female pelvic tumors by applying the clinical diagnostic tools.Materials and methods. Four rare clinical cases were analyzed; all of them posed difficulties in interpreting the diagnostic examination due to their atypical characteristics. There were 2 cases of ovarian cancer, initially identified by an experienced team of radiologists as benign pelvic pathology. Also, there were fibroids with degeneration, marked proliferative activity, and a massive inflammatory reaction of the peritoneum – that was diagnosed as a malignant ovarian tumor. Tumor biopsies were examined using morphological and immunohistochemical methods (with the р16, Ki-67, p53, CD 117, S 100, CD 34 markers). Immunohistochemical (IHC) studies were performed with formalin-fixed paraffin materials using the avidin-biotin-peroxidase method. Antibodies to estrogen receptor (ER), progesterone receptor (PR), cytokeratin 7 (CK7), cytokeratin 20 (CK20) and Wilms tumor protein 1 (WT1) were also used.Results. A thorough analysis of the clinical picture and a joint multidisciplinary discussion (gynecologist, oncologist, radiologist, etc.) made it possible to avoid diagnostic errors.Conclusion. These observations demonstrate the difficulties of differential diagnosis between ovarian metastases of uterine cancer and primary multiple ovarian and uterine cancer, as well between leiomyosarcoma and uterine myoma with high mitotic activity. Obviously, the change in diagnosis calls for a change in the treatment strategy.


2021 ◽  
Vol 12 (1) ◽  
pp. 95-98
Author(s):  
I. D. Pokladov ◽  
O. N. Chernova ◽  
A. V. Vazhenin ◽  
R. E. Shtentsel

Pelvic tumors are quite common. Of these, angiofibromas are very rare. It is causes difficulties in differential diagnosis. But getting the right diagnosis is important, given the great similarity with other, often malignant tumors. According to the literature, the average size of angiofibromas does not exceed 12 cm. We present the case of a patient with an unusually large angiofibroma.


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.


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