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Relevant bibliographies by topics / Sclerosing stromal tumour

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Academic literature on the topic 'Sclerosing stromal tumour'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Sclerosing stromal tumour"

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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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Silva, R., N. Sousa, N. B. Charepe, P. Pinto, M. D. Bernardo, and D. Djokovic. "VP04.14: Sclerosing stromal tumour." Ultrasound in Obstetrics & Gynecology 58, S1 (2021): 107–8. http://dx.doi.org/10.1002/uog.24074.

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Ashida, Y., T. Suzuki, G. Shimizu, H. Yanase, T. Anjiki, and K. Kadota. "Sclerosing Stromal Tumour in a Cow." Journal of Veterinary Medicine Series A 42, no. 1-10 (1995): 27–34. http://dx.doi.org/10.1111/j.1439-0442.1995.tb00352.x.

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4

Fotedar, V., M. K. Gupta, R. K. Seam, and A. Tiwari. "Sclerosing stromal tumour of the ovary." Southern African Journal of Gynaecological Oncology 4, no. 2 (2012): 66–68. http://dx.doi.org/10.1080/20742835.2012.11441198.

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Kawamura, Nobuko, Itsuma Kamoi, and Ritsuo Shigyo. "Sclerosing stromal tumour of the ovary." British Journal of Radiology 60, no. 718 (1987): 1031–33. http://dx.doi.org/10.1259/0007-1285-60-718-1031.

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Joty, Fahmida Sharmin, Farhana Dewan, Fahmida Khan Lima, Bipul Biswas, and Eva Rani Nondi. "Sclerosing Stromal Tumour of Ovary- A Case Report." Bangladesh Journal of Obstetrics & Gynaecology 30, no. 1 (2016): 56–58. http://dx.doi.org/10.3329/bjog.v30i1.30510.

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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. Approximately 100 cases reported since first described in 1973. It typically present with pelvic/abdominal pain and tenderness, mass, and/or abnormal menses, and with hormonal activity reported predominantly in postmenarchal females. Only 5 cases of these tumors have been reported in premenarchal girls.We report a case of a 18-year-old girl who developed a sclerosing stromal tumor of ovary and presented with excessive menstruation, pelv

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Ali, Aun, Madeeha Shahid, Shazadi Neelum Agha, Hurais Malik, Sidra Farishta, and Muhammad Hudaib. "A Rare Case of High-Grade Intracholecystic Papillary Neoplasm in the Gallbadder." Journal of Bahria University Medical and Dental College 13, no. 04 (2023): 308–10. http://dx.doi.org/10.51985/jbumdc2023210.

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ICPN is described as a grossly apparent, intraluminal developing mass-forming tumour that is histologically lined by epithelia that exhibit papillary/villous lesions as well as tubular structures with fine fibrovascular stalks and little intervening stroma. In addition, the term "ICPN with stromal invasion" also refers to ICPNs that exhibit microscopically discernible stromal invasion without nodular sclerosing reaction in the wall

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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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9

Rahman, Papiya, Sadia Afroz, Ummey Salma Shabnam, Umama Tun Nesa Emita, Bishnu Pada Dey, and Ferdousy Begum. "Ovarian sclerosing stromal tumour: Report of a new entity with immunohistochemical study." Bangladesh Journal of Medical Science 22, no. 3 (2023): 712–17. http://dx.doi.org/10.3329/bjms.v22i3.65337.

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Sclerosing stromal tumour (SST) is a rare benign sex cord stromal tumour occurring in women in their second and third decades. Patients usually present with menstrual irregularity and pelvic pain. Microscopically, this tumour is characterized by epithelioid and spindle cells arranged in pseudolobules separated by areas with fibrous deposition of various amount. Presence of ‘staghorn like’ proliferating vasculature is the hallmark feature of this tumour. The main differential diagnoses are thecoma and fibroma. Immunohistochemistry can be used to differentiate these tumours. This relatively new

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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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<strong>Background:</strong> 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. <strong>Objectives:</strong> This study has been done to find out the frequencies of various subtypes of these tumours and their histopathological spectrum. <strong>Methods:</strong>

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Book chapters on the topic "Sclerosing stromal tumour"

1

Mocellin, Simone. "Ovarian Sclerosing Stromal Tumor." In Soft Tissue Tumors. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-58710-9_195.

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Zhao, Shuhui. "Ovarian Sclerosing Stromal Tumor." In MRI of Gynaecological Diseases. Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-3644-1_18.

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"Sclerosing Stromal Tumor." In Diagnostic Pathology: Soft Tissue Tumors. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37675-4.50201-5.

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"Sclerosing Stromal Cell Tumor." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-46875-3_102059.

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Jong Kim, Chan, and Young Jong Woo. "Sclerosing Stromal Tumor of the Ovary with Masculinizing in a Premenarchal Girl." In The Endocrine Society's 92nd Annual Meeting, June 19–22, 2010 - San Diego. Endocrine Society, 2010. http://dx.doi.org/10.1210/endo-meetings.2010.part3.p14.p3-682.

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Conference papers on the topic "Sclerosing stromal tumour"

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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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Müller, J., M. Stanik, R. Schatz, et al. "Sclerosing stromal tumor of the ovary: clinicopathological and immunhistochemical characteristics of eight cases." In Kongressabstracts zur 16. Jahrestagung der Mitteldeutschen Gesellschaft für Frauenheilkunde und Geburtshilfe e.V. (MGFG). Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1769880.

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Aguiar, Valentina Barros Braccini de, Betina Vollbrecht, Fernanda Wagner, Letícia Sarah de Azevedo, and Paula Paim Grippa. "Post-radiation morphea as a complication of treatment for invasive ductal carcinoma: a case report." In XXVI Brazilian Mastology Congress. Mastology, 2024. https://doi.org/10.29289/259453942024v34s2066.

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Introduction: Invasive ductal carcinoma (IDC) is the most common histological type of breast cancer, accounting for between 80% and 90% of cases. Treatment typically involves surgical removal of the tumor. Depending on the staging of the disease, hormonal therapy, chemotherapy, or radiotherapy (RT) may be necessary. Although RT has proven to be an excellent therapy for IDC, significantly reducing local recurrence and increasing survival rates, only about 10% of cases are without complications. Post-radiation morphea (PRM), also known as localized scleroderma, is a rare complication associated

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