scholarly journals A rare case of sclerosing stromal tumor of ovary with Meigs syndrome presenting with torsion

2014 ◽  
Vol 5 (4) ◽  
pp. 116-118
Author(s):  
Ketaki K Junnare ◽  
Pramod Tajne ◽  
Pushpalata R Naphade

A young primi para presented with a large solid ovarian mass with ascites and hydrothorax. She had raised CA 125 levels. She developed torsion of the mass after admission. At laparotomy the tumor was subjected to frozen section. The tumor was benign sclerosing stromal tumor of ovary. Uterus and normal ovary could be conserved. DOI: http://dx.doi.org/10.3126/ajms.v5i4.9518 Asian Journal of Medical Sciences 2014 Vol.5(4); 116-118

2013 ◽  
Vol 40 (3) ◽  
pp. 883-886 ◽  
Author(s):  
Maral Mokhtari ◽  
Mojgan Akbarzadeh-Jahromi ◽  
Fatemeh Sari-Aslani ◽  
Bahareh Hamedi ◽  
Mandana Bagheri ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Menka Khanna ◽  
Ashish Khanna ◽  
Mridu Manjari

Sclerosing stromal tumor (SST) is an extremely rare and distinctive sex cord stromal tumor which occurs predominantly in the second and third decades of life. We report a case of a 32-year-old woman who developed a sclerosing stromal tumor of ovary and presented with irregular menstruation and pelvic pain. Her hormonal status was normal but CA-125 was raised. She was suspected to have a malignant tumor on computed tomography and underwent bilateral salpingo-oopherectomy. It is therefore necessary to keep in mind the possibility of sclerosing stromal tumor in a young woman.


2006 ◽  
Vol 32 (6) ◽  
pp. 619-622 ◽  
Author(s):  
Nan Hee Jung ◽  
Tak Kim ◽  
Hai Joong Kim ◽  
Kyu Wan Lee ◽  
Nak Woo Lee ◽  
...  

2019 ◽  
Vol 2019 ◽  
pp. 1-4
Author(s):  
Minh Nguyen ◽  
Namarig Soumit ◽  
Abdul Waheed ◽  
Jack Sees ◽  
Erum Azhar

Sclerosing stromal tumor (SST) is a rare benign neoplasm of the ovary. There are only a few cases of sclerosing stromal tumor of the ovary during pregnancy that have been reported in the literature. The presenting symptoms are nonspecific, including pelvic pain or menstrual irregularities. We describe a case of a young 22-year-old pregnant woman who presented with pelvic pain in the second trimester. On imaging she was found to have a 12 cm left adnexal mass with solid features on MRI. The patient underwent exploratory laparotomy and removal of the mass that was attached to the left ovary via a stalk with preservation of the left ovary. The frozen section diagnosis was “sex cord stromal tumor, favor benign”. The final pathology confirmed the diagnosis of the sclerosing stromal tumor of the ovary where characteristic features of SST including a heterogenous, pseudolobular growth pattern with hypercellular and hypocellular areas were identified along with prominent luteinized stromal cells attributed to pregnancy. In this case report and review of literature, we emphasize consideration of this rare ovarian tumor in the differential diagnosis for a young pregnant woman who presents with pelvic pain.


2017 ◽  
Vol 25 (8) ◽  
pp. 739-744
Author(s):  
Meral Uner ◽  
Alp Usubutun

Sclerosing stromal tumors of the ovary are very rare. We report the case of a 29-year-old pregnant woman who presented with a history of preterm labor and gestational hypertension. A huge mass measuring 30 cm in greatest dimension was recognized on the right ovary during cesarean section. Signet ring cell infiltration was seen during intraoperative frozen section consultation. She underwent a right salpingo-oophorectomy, and the permanent diagnosis was sclerosing stromal tumor infiltrated by signet ring cells. Pregnancy-related changes were seen in tumor morphology. Signet ring cells were immunoreactive with antibodies MUC5ac, MUC2, and EMA. Thus, stromal cells were immunoreactive with antibodies inhibin and calretinin. Endoscopic biopsy of the stomach showed a signet ring cell carcinoma, from which the metastasis had originated. This is the first reported case in the literature, and is notable for its challenging differential diagnosis, which included a pregnancy luteoma and primary signet ring stromal tumor of the ovary.


2019 ◽  
Vol 4 (3) ◽  
pp. 127-130
Author(s):  
Malihe Hasanzadeh ◽  
Fereshteh Bazmi ◽  
Parnian Malakuti ◽  
◽  
◽  
...  

Author(s):  
Priyanka Kathuria ◽  
Garima Yadav ◽  
Pratibha Singh

The aim of this study is to report a rare case of ovarian cystadenofibroma with even scarcely observed mucinous type histopathological variant and to discuss the modalities which can contribute to prevent misdiagnosing it as a malignant tumor that may inappropriately lead to aggressive surgical interventions. A 40-year-old female presented with pain in lower abdomen and dysmenorrhea of 3 months duration and a large right adnexal mass which had all the features suggestive of malignancy in pre-operative investigations and even on gross overview and cut section. On the contrary histopathology reports confirmed its benign nature and reported it as mucinous cystadenofibroma. Role of Preoperative MRI and intraoperative frozen section cannot be overemphasized in distinguishing ovarian cystadenofibroma from malignant tumors, which can avoid an unnecessary extensive surgery.


2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Anjani Naidu ◽  
Betty Chung ◽  
Mitchell Simon ◽  
Ian Marshall

Sclerosing stromal tumor of the ovary is a rare, benign, sex cord stromal tumor occurring predominantly in younger women in the 2nd and 3rd decades of life. It typically presents unilaterally with only 2 previously reported cases of bilateral presentation. Common clinical presentations include pelvic or abdominal pain, a mass, or menstrual changes. Although occasionally presenting with hormonal manifestations, virilization as a result of androgen production by the tumor is rare. Here we present an extremely rare case of a sclerosing stromal ovarian tumor in a 14-year-old patient with bilateral presentation and with clinical and biochemical evidence of hyperandrogenemia.


2006 ◽  
Vol preprint (2007) ◽  
pp. 1
Author(s):  
Odette Hall ◽  
Judy Pascasio ◽  
Jennifer Morrissette ◽  
Christopher Newton ◽  
Marshall Schwartz ◽  
...  

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