Gotowe bibliografie tematyczne / Sex cord stromal tumour

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Gotowa bibliografia na temat „Sex cord stromal tumour”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Sex cord stromal tumour"

Shweta. "Sclerosing Stromal Tumor of Ovary: A Rare Case Report." International Journal of Health Sciences and Pharmacy (IJHSP) 1, no. 2 (2017): 11–15. https://doi.org/10.5281/zenodo.836195.

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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 histom

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Aditi, Sanjay Sakarkar, and Shivaji Unde Mukund. "Retrospective Study of Histopathological Spectrum of Ovarian Sex Cord Stromal Tumours at Tertiary Care Hospital – A Three Year Study." International Journal of Pharmaceutical and Clinical Research 14, no. 8 (2022): 605–9. https://doi.org/10.5281/zenodo.13357540.

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Background: Sex cord-stromal tumours of the ovary are rare tumours as compared to epithelial tumours of the ovary showing variable histological and biological patterns. Adolescence and young adults are the two age groups in which these tumours are frequently found except for adult granulosa cell tumour which is typically found to develop later i.e. at the age of 50 to 55 years. Objectives: This study has been done to find out the frequencies of various subtypes of these tumours and their histopathological spectrum. Methods:

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S.M.Tamaskar. "Ovarian Sex Cord-Stromal Tumours: "Newly Recognised Entities"." PJSR 2, no. 1 (2009): 47–55. https://doi.org/10.5281/zenodo.8279321.

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A sex cord-stromal tumour is one that is composed of granulosa cells, theca cells, Sertoli cells, Leydig cells and fibroblasts of stromal origin, singly or in various combinations. A pseudopapillary pattern has been described recently in granulosa cell tumours. This was seen in both juvenile and adult types. Pseudopapillae develop as a secondary or degenerative phenomenon lacking true stromal cores. The distinction of a granulosa cell tumour from a surface epithelial carcinoma can be aided by the use of Epithelial Membrane Antigen (EMA) which is positive in carcinomas and Inhibin and Calretini

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Syeda Iqra Usman, Veena Maheshwari, Sushant Sahui, and Murad Ahmed. "SCLEROSING STROMAL TUMOR: AN INCIDENTAL FINDING IN PATIENT OF INFERTILLITY." International Journal of Histopathological Interpretation 11, no. 2 (2022): 20–24. http://dx.doi.org/10.56501/intjhistopatholinterpret.v11i2.596.

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Ovarian sex cord stromal tumors are infrequent and represents only 7% of all ovarian neoplasm. Cells of origin of these tumors are primitive sex cords or stromal cells. The stromal cells comprise of theca cells, fibroblasts and Leydig cells whereas the gonadal primitive sex cords include granulosa cells and Sertoli cells. According to recent WHO classification sex cord stromal tumors are further subdivided into pure stromal tumors, pure sex cord tumors and mixed sex cord stromal tumors. Here we are going to discuss a rare case of pure stromal tumors i.e., Sclerosing stromal tumor.

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Permi, Harish S., Shetty K. Padma, Supriya Rai, Lakshmi Manjeera, Neetha Poojary, and Teerthanath S. "AN UNUSUAL CYTOLOGICAL EXPERIENCE OF VIRILISING OVARIAN SERTOU-LEYDIG CELL TUMOR - A RARE CASE REPORT." Journal of Health and Allied Sciences NU 03, no. 01 (2013): 63–65. http://dx.doi.org/10.1055/s-0040-1703636.

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AbstractSertoli-Leydig cell tumor of ovary is a gonadal tumour of the sex cord-stromal type. It is a rare tumor comprising 0.1 to 0.5% of all ovarian tumours. Peritoneal cytology has been well established as a diagnostic and staging tool in the management of the common epithelial tumours of ovary. Germ cell, mesenchymal, and sex-cord stromal tumours are much less frequently encountered in peritoneal specimens, often with cytologic features that may pose diagnostic difficulty and dilemma. We report a case of peritoneal fluid cytology of sertoli leydig cell tumor of ovary in a 20 year old female

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Thomas, Alina Ajoy, Meeta Thomas, Rebecca Mathews, and Lillykutty Pothen. "Ovarian sclerosing stromal tumour in a 39-year-old lady- A case report and review of the literature." Indian Journal of Pathology and Oncology 9, no. 2 (2022): 180–83. http://dx.doi.org/10.18231/j.ijpo.2022.042.

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One of the rarest ovarian sex cord-stromal tumour is Sclerosing Stromal Tumour (SST). It commonly presents as lower abdominal pain and tenderness, with or without a mass, and/or abnormal menses. As the clinical presentation and imaging are like borderline or malignant epithelial tumours and sex cord-stromal tumours, accurate preoperative clinical diagnosis can be a challenge and the diagnosis is usually made following postoperative histopathologic examination. Understanding the clinicopathological characteristics of this tumour is vital for accurate preoperative diagnosis, which can be essenti

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Mahendran, Revathy, and Madurai Padmanaban Kanchana. "Ovarian fibrothecoma with minor sex cord elements: a case report." International Journal of Research in Medical Sciences 8, no. 4 (2020): 1551. http://dx.doi.org/10.18203/2320-6012.ijrms20201358.

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Ovarian fibroma is the most common sex cord stromal tumour of ovary accounting to 1-5% of all ovarian tumours. Minor sex cord elements in ovarian fibroma are a rare entity occupying less than 10% of tumour area. To the best of our knowledge only 20 cases has been reported till date. This case is presented because of its rarity. Authors reported a case of fibrothecoma with minor sex cord elements in a 70yr old postmenopausal women who presented with postmenopausal bleeding with abdominal mass.

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Palmieri, Vincent, Husain Al-Mahmeed, and Peter Metrakos. "Bilateral liver metastases from testicular sex cord-stromal tumour." BMJ Case Reports 12, no. 5 (2019): e228857. http://dx.doi.org/10.1136/bcr-2018-228857.

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A 28-year-old man previously diagnosed and treated for testicular sex cord-stromal tumour (TSCST) presented with symptoms of fever, night sweats and fatigue. Following initial investigations for an infectious aetiology, imaging studies detected two large liver lesions. Histopathological assessment of the tumours revealed that they were metastases from the TSCST for which the patient had radical inguinal orchiectomy and retroperitoneal lymph node dissection 5 years prior. The curative-intent management of the bilobar liver metastases necessitated staged resection due to the chemoresistant and r

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Hoogland, Marije, Ivar Bleumer, and Albert Suurmeijer. "Microcystic stromal tumour of testis." BMJ Case Reports 15, no. 3 (2022): e248498. http://dx.doi.org/10.1136/bcr-2021-248498.

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Within the group of gonadal sex cord-stromal tumours, microcystic stromal tumour (MCST) is a rare entity. In the literature, most case series and reviews discussed MCST arising in the ovary, only one case-report concerned a testicular MCST. We present a Caucasian man in his late 30s, who presented with an MCST in his right testis. The tumour was encapsulated and composed of vaguely lobulated cellular nodules and cystic spaces with bland spindle cells and hyalinised fibrous stroma. By immunohistochemistry, the tumour cells expressed cluster designation 10, androgen receptor, steroidogenic facto

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Balathil, Ranjana, Ajitha Pulpra, Rabiyabi Vethavayal, and Ani Praveen. "Steroid cell tumour-a rare ovarian tumour: a case report." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 13, no. 10 (2024): 2927–29. http://dx.doi.org/10.18203/2320-1770.ijrcog20242834.

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Steroid cell tumours of the ovary are sex cord stromal tumours which are rare, of all ovarian tumours. Case: Here we present a case of 35-year-old lady who presented to us with complaints of amenorrhoea. With thorough history taking, diagnostic workup and postoperative histopathological evaluation found to have a rare kind of ovarian tumor steroid cell tumor.

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Rozprawy doktorskie na temat "Sex cord stromal tumour"

Yance, Viviane dos Reis Vieira. "Contribuição das características clínicas, hormonais e radiológicas para o diagnóstico diferencial dos tumores de ovário produtores de andrógenos e hipertecose do estroma ovariano em mulheres na pós-menopausa." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-24102016-143113/.

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Introdução: Hiperandrogenemia associada a sinais clínicos de virilização na mulher após a menopausa é uma condição rara e pouco estudada. Os tumores ovarianos secretores de andrógenos (TOSA) e a hipertecose do estroma ovariano (HPT) são as etiologias mais frequentes de hiperandrogenismo nesta faixa etária. A diferenciação entre estas duas condições é difícil, pois as manifestações clínicas são semelhantes e caracterizadas por hirsutismo, alopecia androgênica, clitoromegalia, hipertrofia muscular e agravamento da voz. O perfil hormonal das mulheres pós-menopausadas com TOSA e HPT pode não ser u

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郭智. "Sex cord-stromal tumors of the ovary-a clinicopathological study." Thesis, 1987. http://ndltd.ncl.edu.tw/handle/04461838950748750897.

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Książki na temat "Sex cord stromal tumour"

Chapman, Hannah, and Christine Elwell. Ovarian and testicular cancer. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0328.

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Ovarian cancer is the fifth most common cancer in females in the UK. In contrast, testicular cancer is a rare disease: there were 2138 new cases of testicular cancer diagnosed in 2008 in the UK, and only 70 deaths. Ninety per cent of all ovarian cancers are of epithelial origin, although germ cell and sex cord–stromal cell tumours also occur. In contrast, 95% of testicular cancers are germ cell tumours, with stromal cell tumours and lymphomas making up the remaining 5%. This chapter discusses ovarian cancer and testicular cancer, including definitions of the diseases and their etiologies, typi

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Części książek na temat "Sex cord stromal tumour"

Brown, Jubilee, and David M. Gershenson. "Sex Cord-Stromal Tumors." In Rare and Uncommon Gynecological Cancers. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-13492-0_10.

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Nistal, Manuel, and Pilar González-Peramato. "Sex Cord-Stromal Tumors." In Atlas of Peculiar and Common Testicular and Paratesticular Tumors. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-19654-7_3.

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Ganesan, Raji. "Sex Cord–Stromal Tumors." In Pathology of the Ovary, Fallopian Tube and Peritoneum. Springer London, 2014. http://dx.doi.org/10.1007/978-1-4471-2942-4_15.

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Lastra, Ricardo R., and Raji Ganesan. "Sex Cord-Stromal Tumors." In Essentials of Diagnostic Gynecological Pathology. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-39659-5_26.

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Buy, Jean Noel, and Michel Ghossain. "Sex Cord-Stromal Tumors." In Gynecological Imaging. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-31012-6_11.

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Hui, Pei, and Natalia Buza. "Ovarian Sex Cord-Stromal Tumors." In Atlas of Intraoperative Frozen Section Diagnosis in Gynecologic Pathology. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-21807-6_10.

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Vrdoljak-Mozetič, Danijela, and Vesna Mahovlić. "Sex Cord-Stromal Tumors, Cytological Findings." In Encyclopedia of Pathology. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-33286-4_980.

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Barry, Marc, Arpit Rao, and Richard Lauer. "Sex Cord-Stromal Tumors of the Testis." In Rare Genitourinary Tumors. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-30046-7_16.

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Schultz, Kris Ann P., Lindsay Frazier, and Dominik T. Schneider. "Ovarian and Testicular Sex Cord-Stromal Tumors." In Pediatric Germ Cell Tumors. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-38971-9_7.

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Lim, Gkeok Stzuan Diana, and Esther Oliva. "Sex Cord Stromal Tumors of the Ovary." In Diagnostic Pathology of Ovarian Tumors. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-9751-7_14.

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Streszczenia konferencji na temat "Sex cord stromal tumour"

Chopra, Seema. "Sclerosing sex cord stromal tumour of the ovary: A rare variant of ovarian neoplasms in childhood and adolescence." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685321.

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Case Report: 19 yr old unmarried girl c/o abdominal distension, loss of appetite and Irregular menstrual cycles x 5 months. USG: gross ascites, liver, Lobulated isoechoic mass in right adnexa, 7x5 cm, abutting right ovary. CA125: 1297 U/ml. FNAC Degenerated crushed cells & stromal fragments. Few scattered benign oval/spindle cells. Laparoscopy f/b laparotomy: 6 litres of straw colored asciic fluid drained. Uterus, left adnexa normal. Rt ovarian mass 6x7 cm, bilobed, arising from ovary. Solid, stuck in POD Adherent to gut. Right oophrectomy done. CA-125: 22 u/ml on day 6 post op. HPE – Scle

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Iqbal, S. A., H. Shukla, V. Jain, S. Giri, R. Sekhon, and S. Rawal. "Synchronous primary ovarian sex cord tumor and endometrial cancer." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685384.

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Synchronous primary tumors of female genital tract are rare with a rate of about 0.7-1.8% of all gynaecological tumours. Most common primary tumours presenting as synchronous lesions are ovary and endometrium. However, sex cord stromal tumors are rare variety of primary ovarian tumor and synchronous with endometrium is even much rarer. These tumors are detected usually in younger, overweight, nulliparous and perimenopausal female. Synchronous primary tumors of endometrium and ovary have a better prognosis than the either of above alone because these are usually low grade and diagnosed at early

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Kim, SH, A. Da Cruz Paula, EM da Silva, et al. "229 Genetic heterogeneity of ovarian sex cord-stromal tumors." In IGCS Annual 2019 Meeting Abstracts. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/ijgc-2019-igcs.229.

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Savita, Pannu, and Khullar Harsha. "Two interesting cases of granulosa cell tumor: A case report." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685326.

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Introduction: Granulosa cell tumor (GCT) is an ovarian malignancy that arise from granulosa cells of the ovary. This tumour is a type of the sex cord-gonadal stromal tumour. GCT have good prognosis in comparison with other epithelial tumors. Methodology: Two cases of granulosa cell tumors were diagnosed in sir Ganga ram hospital, Rajendernagar, New Delhi in December 2015 and January 2016. The patient’s age, clinical manifestations, radiological and histopathological findings were evaluated. One was in perimenopausal age group and other case was in postmenopausal age group. The clinical manifes

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Introduction: Granulosa cell tumor (GCT) is an ovarian malignancy that arise from granulosa cells of the ovary. This tumour is a type of the sex cord-gonadal stromal tumour. GCT have good prognosis in comparison with other epithelial tumors. Methodology: Two cases of granulosa cell tumors were diagnosed in sir Ganga ram hospital, Rajender Nagar, New Delhi in December 2015 and January 2016. The patient’s age, clinical manifestations, radiological and histopathological findings were evaluated. One was in perimenopausal age group and other case was in postmenopausal age group. The clinical manife

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Ratnaparkhi, R., C. Liao, A. Chan, et al. "299 Increasing incidence of sex cord-stromal tumors in the United States." In IGCS 2020 Annual Meeting Abstracts. BMJ Publishing Group Ltd, 2020. http://dx.doi.org/10.1136/ijgc-2020-igcs.258.

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Fielding, Jordan, and Edgar Martinez-Salazar. "Ovarian stromal and sex cord tumours: reviewing common findings through an uncommon case." In Radiopaedia 2023. Radiopaedia.org, 2023. http://dx.doi.org/10.53347/rposter-1679.

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Hena, Kausar, Manchanda Rahul, Lekhi Anshika, Chitra C. H. Sravani, and Jain Nidhi. "Granulosa cell tumour of ovary in a benign looking adnexal mass: A rare occurrence and its management." In 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685402.

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Granulosa cell tumours are sex cord stromal tumours of the ovary which accounts for 1-2% of all ovarian malignancies. We present a case of a 22 yrs old unmarried girl with chief complaints of dysmenorrhoea for last 4 months. There were no other symptoms and her general physical examination revealed no abnormality. Ultrasonography showed a simple ovarian cyst of 7 x 8 cm in right adnexa with normal Doppler flow and no ascites. Her tumour markers were negative. Per-operative uterus and left sided ovary and upper abdomen was normal. Right ovary showed a simple unilocular cyst of around 8 x 8 cm a

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Bacha, D., A. Ben Amor, A. Sassi, et al. "286 Sex cord-stromal tumour with rhadomyosarcomatous contingent heterologous in A 7-year-old girl treated for xeroderma pigmentosum." In IGCS Annual 2019 Meeting Abstracts. BMJ Publishing Group Ltd, 2019. http://dx.doi.org/10.1136/ijgc-2019-igcs.286.

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Hasenburg, A., H. Plett, P. Harter, et al. "855 Treatment strategies, disease recurrence and survival of women with malignant sex cord-stromal cell tumours in Germany." In ESGO 2021 Congress. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/ijgc-2021-esgo.486.

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