Abstract #1007: Androgen Secreting Benign Ovarian Tumor: A Case Report and Review of the Literature

2016 ◽  
Vol 22 ◽  
pp. 231
Author(s):  
Richa Bhattarai ◽  
Bidur Dhakal ◽  
Kelly Wood
Keyword(s):  
Case Report ◽  
Ovarian Tumor ◽  
Review Of The Literature ◽  
Benign Ovarian Tumor

Cystic struma ovarii, a rare form of ovarian tumor – a case report, and review of the literature

2007 ◽  
Vol 148 (48) ◽  
pp. 2285-2287 ◽  
Author(s):  
Gabriella Östör ◽  
Ildikó Tóth ◽  
Zsuzsanna Hrubyné Tóth ◽  
Sándor Bazsa
Keyword(s):  
Case Report ◽  
Ovarian Tumor ◽  
Ca 125 ◽  
Struma Ovarii ◽  
Review Of The Literature ◽  
Rare Form

Az ovarialis strumák a petefészek-teratomák kevesebb mint 3%-át adják. Megjelenhet bennük a pajzsmirigy szinte minden betegsége, és előfordulhat malignitás is. A szerzők esetében egy 31 éves nő bal oldali petefészekcisztáját távolították el, amely az ovariumcarcinoma klinikai tüneteit mutatta, úgymint nagy hasi térfoglalás, ascites, emelkedett szérum-CA 125-szint. A szövettani diagnózis benignus struma ovarii volt. A posztoperatív pajzsmirigyműködés normális maradt.

scholarly journals Meigs' syndrome with elevated CA 125: case report

2003 ◽  
Vol 121 (5) ◽  
pp. 210-212 ◽  
Author(s):  
Sabas Carlos Vieira ◽  
Leonardo Halley Carvalho Pimentel ◽  
José Carlos Castelo Branco Ribeiro ◽  
Argemiro Ferreira de Andrade Neto ◽  
Jerúsia Oliveira Ibiapina de Santana
Keyword(s):  
Case Report ◽  
Pleural Effusion ◽  
Ovarian Tumor ◽  
Frozen Section ◽  
Transvaginal Ultrasound ◽  
Elevated Serum ◽  
Ca 125 ◽  
Brazilian Woman ◽  
Thoracic Drainage ◽  
Benign Ovarian Tumor

CONTEXT: Meigs' syndrome consists of a benign ovarian tumor accompanied by ascites and hydrothorax. Elevated serum CA 125 levels in postmenopausal women with solid adnexal masses, ascites and pleural effusion are highly suggestive for malignant ovarian tumor. However, patients with Meigs' syndrome can also have elevated serum CA 125 levels. The authors report a case of Meigs' syndrome with elevated CA 125 level. OBJECTIVE: This is a case report of Meigs' syndrome with elevated CA 125 level. CASE REPORT: A 65-year-old Brazilian woman had presented progressive dyspnea, weight loss and decline in general condition over the 7 months preceding admission to our service. In another hospital, the patient had been submitted to thoracic drainage due to pleural effusion. With recurrence of the pleural effusion and increase in abdominal volume due to ascites and a pelvic mass, the patient sought our service. Transvaginal ultrasound showed an extensive adnexal solid mass of 16.4 x 10.8 cm located in the pelvis without exact limits, and the serum CA 125 level was elevated. With a preoperative diagnosis of ovarian carcinoma, the patient was submitted to exploratory laparotomy, which revealed a left ovarian tumor. The frozen section diagnosis was thecoma. Total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed. The histology of the specimen confirmed the diagnosis of thecoma. The patient was asymptomatic with a normal serum CA 125 level 20 months after the operation.

Ovarian Serous Cystadenofibroma - A Rare Case Report

2020 ◽  
pp. 23-25
Author(s):  
OJS Admin
Keyword(s):  
Case Report ◽  
Ovarian Tumor ◽  
Rare Case ◽  
Middle Age ◽  
Young Age ◽  
Benign Ovarian Tumor ◽  
Rare Case Report

The uncommon benign ovarian tumor in young age is ovarian cystadenofibroma. It mostly affects women in their middle age.

scholarly journals Contralateral Ovarian Metastasis of Clear-Cell Renal Carcinoma: A Rare Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-3
Author(s):  
Fatih Uruc ◽  
Serkan Akan ◽  
Aytaç Sahin ◽  
Caglar Yildirim ◽  
Ahmet Urkmez
Keyword(s):  
Case Report ◽  
Ovarian Tumor ◽  
Rare Case ◽  
Renal Carcinoma ◽  
Clear Cell ◽  
Ovarian Metastasis ◽  
Review Of The Literature ◽  
Clear Cell Renal Carcinoma ◽  
Cell Renal Carcinoma ◽  
Rare Case Report

Renal cell carcinoma (RCC) constitutes 2-3% of all types of cancers. RCCs metastasize into lungs (50–60%), lymph nodes (36%), bones (30–40%), liver (30–40%), and brain (5%) in respective percentages. RCC rarely metastasizes into ovary. Only 25 cases of ovarian tumor, which metastasized into kidneys, have been presented. In the literature, a kidney-ovary axis has been defined, and its interrelationship begins with embryological life. With this case report, we aimed both to present a very rarely seen metastasis of RCC into contralateral ovary and also to review the literature.

Mixed Ovarian Tumor Composed of Brenner Tumor and Adult-Type Granulosa Cell Tumor: A Case Report of a Very Rare Mixed Ovarian Tumor and a Review of the Literature

2017 ◽  
Vol 26 (4) ◽  
pp. 382-387
Author(s):  
Judit Tamás ◽  
Ildikó Vereczkey ◽  
Erika Tóth ◽  
Erzsébet Csernák ◽  
Katalin Purcsi ◽  
...  
Keyword(s):  
Case Report ◽  
Granulosa Cell ◽  
Ovarian Tumor ◽  
Granulosa Cell Tumor ◽  
Cell Tumor ◽  
Ovarian Tumors ◽  
Review Of The Literature ◽  
Adult Type ◽  
Histologic Subtype ◽  
Brenner Tumor

A combination of ovarian tumors with the same histogenetic origin but different histologic subtype is relatively common, whereas a co-occurrence of tumors with different histogenetic origin is rare. We report a case of mixed ovarian tumor composed of Brenner tumor and adult-type granulosa cell tumor, a combination that to the best of our knowledge has not been reported in the literature until now.

scholarly journals Isolated subcutaneous implantation of a borderline ovarian tumor: A case report and review of the literature

2016 ◽  
Vol 7 (2) ◽  
pp. 270 ◽  
Author(s):  
Malgorzata Banys-Paluchowski ◽  
Borsu Yeganeh ◽  
Jutta Luettges ◽  
Achim Maibach ◽  
Ruediger Langenberg ◽  
...  
Keyword(s):  
Case Report ◽  
Ovarian Tumor ◽  
Borderline Ovarian Tumor ◽  
Review Of The Literature ◽  
Subcutaneous Implantation

scholarly journals Sclerosing Stromal Tumor of Ovary: A Rare Case Report

2017 ◽  
pp. 11-15
Author(s):  
Shweta ◽  
Kuladeepa Ananda Vaidhya ◽  
Sukesh
Keyword(s):  
Case Report ◽  
Blood Vessels ◽  
Ovarian Tumor ◽  
Rare Case ◽  
Rare Tumour ◽  
Stromal Tumors ◽  
Benign Ovarian Tumor ◽  
Ovarian Tumours ◽  
Rare Case Report ◽  
Sclerosing Stromal Tumor

Sclerosing stromal tumour (SST) is a rare benign ovarian tumor of the sex cord stromal type, occurring predominantly in the second and third decades of life. This tumour is characterized microscopically by having a pseudolobular pattern with cellular areas separated by hypocellular densely hyalinised, edematous stroma interspersed with few prominent blood vessels. Histopathological features which differentiate it from other stromal tumors. We are presenting this case because of its rarity and its simulation with various other ovarian tumours; here we have made an effort to highlight the his tomorphological features and microscopic differential diagnoses of this rare tumour

Management of a Giant Ovarian Tumor More Than 30 kg: A Case Report and Review of the Literature

2018 ◽  
Vol 34 (5) ◽  
pp. 243-247 ◽  
Author(s):  
Munetoshi Akazawa ◽  
Toshiaki Saito ◽  
Rina Nagayama ◽  
Kazuya Ariyoshi ◽  
Masao Okadome
Keyword(s):  
Case Report ◽  
Ovarian Tumor ◽  
Review Of The Literature
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