Sclerosing stromal tumour of the ovary

Fotedar, Vikas; Gupta, Manoj Kumar; Seam, Rajeev Kumar; Tiwari, Abhijeet

doi:10.1080/20742835.2012.11441198

Cited by 3 publications

(16 citation statements)

References 1 publication

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“…Similar results have been reported with the disappearance of menstrual irregularity with excision of the tumour. 2,8,9 This could be a rare case of hormonally active SST. Hormonal assay was not done because SST was least suspected in the mesentery.…”

Section: 45mentioning

confidence: 96%

“…The commonest symptom is menstrual irregularity which is reported to disappear after surgical excision of the tumour. 2,8,9 Other symptoms include pelvic pain, and non specific pain related to ovarian mass. The tumours may, in rare cases, cause masculinisation, anovulation and infertility.…”

Section: 45mentioning

confidence: 99%

“…2,[8][9][10] In this case the patient presented with irregular menses and secondary infertility. Complete excision of the tumour resulted in normalisation of the menses and subsequent conception and delivery.…”

Section: 45mentioning

confidence: 99%

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Extra gonadal sclerosing stromal tumour in the transverse mesocolon

Mensah¹,

Kyei²,

Ohene-Yeboah³

et al. 2016

Ghana Medical Journal

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SUMMARYSclerosing stromal tumour (SST) is a rare benign sex cord stromal tumour of the ovary. We report a case of sclerosing stromal tumour of the mesentery in a 32-year-old Para one who presented with intra abdominal mass, menstrual irregularity and secondary infertility. Histopathology and immunohistochemistry of the completely excised tumour was consistent with sclerosing stromal tumour, immunoreactive only to vimentin. No ovarian tissue was found in the sectioned tumour. Her menses became regular and she conceived 3 months after complete excision and delivered after 9 months. Hormonal assay was not done because SST was least suspected. From literature this is the first case of SST in the transverse mesocolon reported in the West African subregion, and may probably be one of the rare cases of hormonally active SST.

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Section: 45mentioning

confidence: 96%

Section: 45mentioning

confidence: 99%

See 1 more Smart Citation

Extra gonadal sclerosing stromal tumour in the transverse mesocolon

Mensah¹,

Kyei²,

Ohene-Yeboah³

et al. 2016

Ghana Medical Journal

View full text Add to dashboard Cite

show abstract

“…Sclerosing stromal tumor (SST) is a rare subtype of ovarian sex cord stromal tumor occurring predominantly in the second and third decades of life . Reported cases followed a benign course and recurrence has not been reported .…”

Section: Introductionmentioning

confidence: 99%

“…This tumor is usually unilateral and the most frequent presentation is menstrual irregularities. The other symptoms including pelvic pain, non‐specific symptoms related to ovarian mass, hirsutism and masculinization …”

Section: Introductionmentioning

confidence: 99%

Extragonadal sclerosing stromal tumor: A rare case report

Mokhtari

Akbarzadeh‐Jahromi

Aslani

et al. 2013

J of Obstet and Gynaecol

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Sclerosing stromal tumor is a rare, benign, sex cord stromal tumor of the ovary. We report a case of extragonadal sclerosing stromal tumor in a 45-year-old woman who presented with menstrual irregularity and vague pelvic pain. Imaging studies showed a well-defined mass between the posterior wall of the bladder and uterus, suspected of being a pedunculated leiomyoma. The histopathological and immunohistochemical study was consistent with sclerosing stromal tumor. No ovarian tissue was found on representative sectioning. This is the first case of sclerosing stromal tumor in an extragonadal location.

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Sclerosing Stromal Tumor: A Rare Ovarian Neoplasm

Bairwa¹,

Satarkar²,

Kalhan³

et al. 2017

Iran J Pathol

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Ovarian sex cord-stromal tumors are relatively infrequent neoplasms that account for approximately 8% of all primary ovarian neoplasm. Sex cord-stromal tumors of the ovary include granulosa cell tumors, fibrothecomas, Sertoli-Leydigcell tumors, steroid cell tumors, and sclerosing stromal tumors (SST). Sclerosing stromal tumors account for 2% to 6% of ovarian stromal tumors. Despite the rarity of this particular neoplasm, it is not always possible to predict the presence of this tumor preoperatively on the basis of clinical and sonographic findings. Histopathological and immunohistochemical (IHC) examinations confirm the diagnosis. Herein, the clinical findings and histopathological features of SST are described in a 24-year-old female.

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Sclerosing stromal tumour of the ovary

Cited by 3 publications

References 1 publication

Extra gonadal sclerosing stromal tumour in the transverse mesocolon

Extra gonadal sclerosing stromal tumour in the transverse mesocolon

Extragonadal sclerosing stromal tumor: A rare case report

Sclerosing Stromal Tumor: A Rare Ovarian Neoplasm

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