Log in

Relevant bibliographies by topics / Sclerosing stromal tumour / Journal articles

To see the other types of publications on this topic, follow the link: Sclerosing stromal tumour.

Journal articles on the topic 'Sclerosing stromal tumour'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Sclerosing stromal tumour.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

2

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

8

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

Abstract:

<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>

APA, Harvard, Vancouver, ISO, and other styles

11

Latincic, Stojan, Natasa Colovic, Marjan Micev, and Radoje Colovic. "Pendular stromal tumour of the stomach with dominant PDGFRA immunoexpression: Case report and short literature review." Srpski arhiv za celokupno lekarstvo 140, no. 3-4 (2012): 216–20. http://dx.doi.org/10.2298/sarh1204216l.

Full text

Abstract:

Introduction. Gastrointestinal stromal tumours are most frequent mesenchimal tumours of the gastrointestinal tract that originate from Cajal?s interstitial cells that are most frequently CD-117 positive. Stromal tumours of the stomach are the most frequent mesenchimal tumours of the gastrointestinal tract. Such tumours are usually sessile, but rarely pendular when they can be easily removed with a limited local excision of the stomach wall around the pedicle. Major stomach resections are rarely necessary. Case Outline. In a 54-year-old woman with abdominal pain and fever of unknown aetiology,

APA, Harvard, Vancouver, ISO, and other styles

12

De Silva, M. V. C., and L. R. Amarasekera. "Sclerosing stromal tumour of the ovary: a case report." Ceylon Journal of Medical Science 39, no. 2 (1996): 57. http://dx.doi.org/10.4038/cjms.v39i2.4898.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Mensah, Samuel, Ishmael Kyei, Michael Ohene –Yeboah, and Ernest Adjei. "Extra gonadal sclerosing stromal tumour in the transverse mesocolon." Ghana Medical Journal 50, no. 1 (2016): 57. http://dx.doi.org/10.4314/gmj.v50i1.9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Karabulut, A., N. Karabulut, and M. Akbulut. "Ovarian sclerosing stromal tumour with elevated CA19-9 levels." Journal of Obstetrics and Gynaecology 35, no. 2 (2014): 215–16. http://dx.doi.org/10.3109/01443615.2014.940289.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Deen, Suha, Ashu Loona, and David O’Neill. "Ovarian Sclerosing Stromal Tumour Presenting with Pseudo-Meigs' Syndrome." International journal of Gynecology, Obstetrics and Neonatal Care 2, no. 1 (2015): 31–33. http://dx.doi.org/10.15379/2408-9761.2015.02.01.7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

17

LIFSCHITZ-MERCER, B., M. OPEN, I. KUSHNIR, N. JACOB, B. CASPI, and B. CZERNOBILSKY. "Hyaline globules and progesterone receptors in an ovarian sclerosing stromal tumour." Histopathology 27, no. 2 (1995): 195–97. http://dx.doi.org/10.1111/j.1365-2559.1995.tb00031.x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Singh, Rajinder, Yasmin Muhammed, Ajay Shanker Sharma, and Jasbir Singh. "Gastrointestinal stromal tumour-sclerosing epithelioid a rare variant: A case report." International Journal of Clinical and Diagnostic Pathology 6, no. 2 (2023): 87–89. http://dx.doi.org/10.33545/pathol.2023.v6.i2b.522.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Pinto, Karen, and Runjan Chetty. "Gene of the month: TFE 3." Journal of Clinical Pathology 73, no. 11 (2020): 691–94. http://dx.doi.org/10.1136/jclinpath-2020-206899.

Full text

Abstract:

Transcription factor enhancer 3 (TFE3), on the short arm of chromosome Xp11.23 and its protein, belongs to the microphthalmia transcription family (MiTF) of transcription factors. It shares close homology with another member of the family, MiTF which is involved in melanocyte development. When a cell is stressed and/or starved, TFE3 protein translocates into the nucleus. TFE3 gene fusions with multiple different partner genes occur in several tumours with resultant nuclear expression of TFE3 protein. The main tumours associated with TFE3 gene fusions are: renal cell carcinoma, alveolar soft pa

APA, Harvard, Vancouver, ISO, and other styles

20

Costa, C., A. Costa, P. Baptista, and V. Paiva. "Sclerosing stromal tumour of the ovary associated with Meigs' syndrome and elevated CA125." Journal of Obstetrics and Gynaecology 30, no. 7 (2010): 747–48. http://dx.doi.org/10.3109/01443615.2010.498532.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Chaurasia, J. K., N. Afroz, V. Maheshwari, and M. Naim. "Sclerosing stromal tumour of the ovary presenting as precocious puberty: a rare neoplasm." Case Reports 2014, mar31 1 (2014): bcr2013201124. http://dx.doi.org/10.1136/bcr-2013-201124.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Özdemir, Özhan, MustafaErkan Sari, Ertugrul Sen, Aslihan Kurt, AyseBurcu Ileri, and CemalResat Atalay. "Sclerosing stromal tumour of the ovary: A case report and the review of literature." Nigerian Medical Journal 55, no. 5 (2014): 432. http://dx.doi.org/10.4103/0300-1652.140391.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Kutuk, M. S., M. T. Ozgun, S. Uludag, I. S. Serin, and H. Akgun. "A case of ovarian sclerosing stromal tumour concomitant with endometrial adenocarcinoma in a postmenopausal woman." Journal of Obstetrics and Gynaecology 33, no. 1 (2012): 97–98. http://dx.doi.org/10.3109/01443615.2012.717990.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Tenkumo, C., U. Hanaoka, K. Kanenishi, and T. Hata. "EP19.10: HDliveFlow silhouette mode with HDlive silhouette mode for diagnosis of sclerosing stromal tumour of the ovary." Ultrasound in Obstetrics & Gynecology 52 (October 2018): 271. http://dx.doi.org/10.1002/uog.20068.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Serinelli, S., G. de la Roza, and D. J. Zaccarini. "A case of TFE-3-positive non-neoplastic pseudodecidualized endometrium presenting as a cervical mass." American Journal of Clinical Pathology 156, Supplement_1 (2021): S109—S110. http://dx.doi.org/10.1093/ajcp/aqab191.233.

Full text

Abstract:

Abstract Introduction/Objective TFE-3 gene encodes a transcription factor that promotes the expression of genes involved in cell growth and proliferation. Its overactivation can result in oncogenic activity. Although TFE-3 seems to be almost universally expressed in normal tissues, this expression should be at very low levels and strong nuclear expression of TFE-3 is seen almost exclusively in tumors containing or lacking the TFE-3 gene fusion. These include renal cell carcinoma, alveolar soft part sarcomas, epithelioid hemangioendotheliomas, PEComas, granular cell tumour, solid pseudopapillar

APA, Harvard, Vancouver, ISO, and other styles

26

Ismail, S. I. M. F., and S. A. Adams. "A large sclerosing stromal tumour of the ovary presenting with irregular uterine bleeding: First case report from the UK." Journal of Obstetrics and Gynaecology 30, no. 3 (2010): 322–23. http://dx.doi.org/10.3109/01443611003638881.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Devi P., Lekshmi, Cicy P. J., Sansho E. U., Deepa S., and Laila Raji N. "Spindle cell lesions of breast: a retrospective analysis with emphasis on diagnostic challenges." International Journal of Advances in Medicine 4, no. 6 (2017): 1627. http://dx.doi.org/10.18203/2349-3933.ijam20175179.

Full text

Abstract:

Background: Spindle cell lesions of breast comprise a rare group of complex entities which may be reactive, benign or malignant. Though definitive diagnosis is difficult especially in small biopsies, it is of utmost importance since the management differs. Precise knowledge of the lesions in this group, thorough sampling, clinic radiological correlation and ancillary techniques will aid in making the correct diagnosis. Review of literature showed only a few extensive studies on spindle cell lesions in breast, especially from South India.Methods: Our research is a descriptive histopathological

APA, Harvard, Vancouver, ISO, and other styles

28

Caro Cuenca, T., A. Sanz Zorrilla, F. Leiva-Cepas, and M. Medina Pérez. "Sclerosant ovary stromal tumor. Differential diagnostic challenge." ACTUALIDAD MEDICA 105, no. 105(811) (2020): 222–25. http://dx.doi.org/10.15568/am.2020.811.cc01.

Full text

Abstract:

We present the case of a stromal ovarian sclerosing tumor in a woman of the third decade of life. These tumors derive from the stroma-sexual cords of the ovary, have a low incidence and exhibit a benign behavior. the available literature is reviewed to date, given the importance of proper differential diagnosis.

APA, Harvard, Vancouver, ISO, and other styles

29

Rana, R., S. U. Kafle, K. K. Jha, M. Singh, and P. Gautam. "Sclerosing Stromal Tumor of Ovary: A Case Report." Birat Journal of Health Sciences 1, no. 1 (2017): 83–86. http://dx.doi.org/10.3126/bjhs.v1i1.17107.

Full text

Abstract:

A case of 32 year old female of pelvic pain for one month and with past history of hysterectomy performed two year back. Clinical examination revealed palpable abdominal pelvic mass. Ultrasonography showed right pelvic mass arising from right adnexa measuring 15cm x 15 cm, predominantly solid with some cystic areas. The patient was suspected of having a malignant ovarian tumor and hence operated. A histopathological diagnosis revealed sclerosing stromal tumor of ovary. Sex cord-stromal tumors account for approximately 8% of all ovarian tumor and prevalence of sclerosing stromal tumor of ovary

APA, Harvard, Vancouver, ISO, and other styles

30

Fathima, S., and K. Mansheim. "Review of Sclerosing stromal tumor: A relatively rare ovarian neoplasm." American Journal of Clinical Pathology 158, Supplement_1 (2022): S90. http://dx.doi.org/10.1093/ajcp/aqac126.188.

Full text

Abstract:

Abstract Introduction/Objective Sclerosing stromal tumor (SST) is sex cord stromal tumor which is rare primary ovarian neoplasm. Because its clinical presentation and imaging findings accurate preoperative clinical diagnosis can be difficult. We report three cases of a sclerosing stromal tumor of ovary and histopathological presentation. Methods/Case Report Our patients had an age ranged from 27-40 years with primary ovarian neoplasm and as incidental in 64-year-old patient. Radiologically lobulated and heterogeneously enhancing, partially calcified masses with nodular rind of avid enhancement

APA, Harvard, Vancouver, ISO, and other styles

31

Khanna, Menka, Ashish Khanna, and Mridu Manjari. "Sclerosing Stromal Tumor of Ovary: A Case Report." Case Reports in Pathology 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/592836.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

32

Herlina, Heni Maulani, and Nursanti Apriyani. "The Relationship of Fibroblast Activation Protein (FAP) Expression to Clinicopathologic Factors of Papillary Thyroid Carcinoma." Majalah Patologi Indonesia 30, no. 3 (2021): 286–94. http://dx.doi.org/10.55816/mpi.v30i3.478.

Full text

Abstract:

BackgroundPapillary thyroid carcinoma is the most common subtype among thyroid cancers. The interaction between cancer cells and tumormicroenvironment plays roles in cancer proliferation and invasiveness. One of important components of tumor microenvironmentthat could stimulate tumor proliferation and invasiveness is activated fibroblast, known as carcinoma associated fibroblasts (CAFs).The aim of this research is to analysed FAP expression is associated with clinicopathologic characteristics.MethodsThis retrospective descriptive observational study with serial cases design was conducted in 40

APA, Harvard, Vancouver, ISO, and other styles

33

Gwin, Katja, Adrián Mariño-Enríquez, Maritza Martel, and Miguel Reyes-Múgica. "Sclerosing Stromal Tumor: An Important Differential Diagnosis of Ovarian Neoplasms in Childhood and Adolescence." Pediatric and Developmental Pathology 12, no. 5 (2009): 366–70. http://dx.doi.org/10.2350/08-10-0545.1.

Full text

Abstract:

Sclerosing stromal tumors are an uncommon type of benign ovarian sex cord-stromal tumor. Histologically, they are characterized by a cellular pseudolobular pattern, composed of fibroblasts and round cells separated by densely collagenous or markedly edematous hypocellular tissue and prominent vascularity. Although the usual age of presentation is in the 2nd and 3rd decades, sclerosing stromal tumor can occur in adolescence or premenarchal girls. Clinical symptoms include premature menarche, menstrual irregularities, abdominal discomfort, and rarely, ascites. Imaging studies frequently reveal s

APA, Harvard, Vancouver, ISO, and other styles

34

Kalita, Lachit, Abhijit Kalita, and Munmun Harlalka. "A Rare Case Report of Serous Cystadenoma with Coexisting Sclerosing Stromal Tumor of Ovary." Annals of Pathology and Laboratory Medicine 10, no. 7 (2023): C78–82. http://dx.doi.org/10.21276/apalm.3256.

Full text

Abstract:

Various forms of collision tumors have been reported in literature before. Ovarian tumors also exhibit different histological components at times. The epithelial neoplasm of ovary in coexistence with sertoli leydig cell tumor, granulosa cell tumor, cystic teratoma and stromal tumor with minor sex cord elements are known to exist. However, literature related to association of serous neoplasm of ovary with sclerosing stromal tumor is not known. We report a case of serous cystadenoma with coexisting sclerosing stromal tumor in a 31-year-old lady which is probably one of the first case reports of

APA, Harvard, Vancouver, ISO, and other styles

35

Naidu, Anjani, Betty Chung, Mitchell Simon, and Ian Marshall. "Bilateral Sclerosing Stromal Ovarian Tumor in an Adolescent." Case Reports in Radiology 2015 (2015): 1–4. http://dx.doi.org/10.1155/2015/271394.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

36

Nguyen, Minh, Namarig Soumit, Abdul Waheed, Jack Sees, and Erum Azhar. "A Rare Case of Sclerosing Stromal Tumor of the Ovary Presenting in Pregnancy: A Diagnostic Dilemma on Presentation." Case Reports in Obstetrics and Gynecology 2019 (December 31, 2019): 1–4. http://dx.doi.org/10.1155/2019/3927971.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

37

Atram, Manisha, Anshu, Satish Sharma, and Nitin Gangane. "Sclerosing stromal tumor of the ovary." Obstetrics & Gynecology Science 57, no. 5 (2014): 405. http://dx.doi.org/10.5468/ogs.2014.57.5.405.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Kawauchi, Shigeto, Takahiro Tsuji, Tsunehisa Kaku, Toshiharu Kamura, Hitoo Nakano, and Masazumi Tsuneyoshi. "Sclerosing Stromal Tumor of the Ovary." American Journal of Surgical Pathology 22, no. 1 (1998): 83–92. http://dx.doi.org/10.1097/00000478-199801000-00011.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Tiltman, A. J. "Sclerosing Stromal Tumor of the Ovary." International Journal of Gynecological Pathology 4, no. 4 (1985): 362–69. http://dx.doi.org/10.1097/00004347-198512000-00009.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Marelli, Guido, Silvestro Carinelli, Andrea Mariani, Luigi Frigerio, and Augusto Ferrari. "Sclerosing stromal tumor of the ovary." European Journal of Obstetrics & Gynecology and Reproductive Biology 76, no. 1 (1998): 85–89. http://dx.doi.org/10.1016/s0301-2115(97)00151-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Khan, Shazia, Virendra Singh, I. D. Khan, and Sujatha Panda. "Sclerosing stromal cell tumor of ovary." Medical Journal Armed Forces India 74, no. 4 (2018): 386–89. http://dx.doi.org/10.1016/j.mjafi.2017.09.007.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Green, Gretchen E., Peter E. Schwartz, and Shirley M. McCarthy. "Sclerosing Stromal Tumor of the Ovary." Journal of Women's Imaging 7, no. 1 (2005): 50–53. http://dx.doi.org/10.1097/01.jwi.0000156344.04127.a0.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

44

Awamleh, Ahlam A., and Bayardo Perez-Ordoñez. "Sclerosing Angiomatoid Nodular Transformation of the Spleen." Archives of Pathology & Laboratory Medicine 131, no. 6 (2007): 974–78. http://dx.doi.org/10.5858/2007-131-974-santot.

Full text

Abstract:

Abstract Sclerosing angiomatoid nodular transformation (SANT) is a recently recognized nonneoplastic vascular lesion of the spleen with fewer than 30 cases described. Microscopically, SANT consists of multiple well-circumscribed vascular/ angiomatoid nodules showing plump endothelial cell and extravasated erythrocytes. The nodules are surrounded by a variable lymphoplasmacytic infiltrate, spindle cells, and collagenous stroma. The vascular nodules display a complex mixture of endothelial phenotypes resembling splenic sinusoids (CD34−/CD31+/CD8+), capillaries (CD34+/ CD31+/CD8−), and small vein

APA, Harvard, Vancouver, ISO, and other styles

45

Longquan, Xiang, and Henry Mwakyoma. "SCLEROSING EPITHELIOID FIBROSARCOMA." Professional Medical Journal 22, no. 03 (2015): 370–73. http://dx.doi.org/10.29309/tpmj/2015.22.03.1359.

Full text

Abstract:

Sclerosing epithelioid fibrosarcoma (SEF) is a rare subtype of Fibrosarcomaand was first reported in 1995. This tumour is rarely encountered and can easily be mistaken byclinicians for other diagnoses. This paper reports one case of SEF and review related literature.Objectives: To determine the clinical pathologic characteristics and discuss differentialdiagnosis of sclerosing epithelioid fibrosarcoma (SEF). Methods: One case of SEF was studiedby clinical analysis, light microscopy and the review of the literature. Results: The patient wasan adult and had a tumor located in the subcutaneous ti

APA, Harvard, Vancouver, ISO, and other styles

46

Turcan, Didem, Funda Canaz, Evrim Yılmaz, Sare Kabukçuoğlu, and Melih Velipaşaoğlu. "Overin Sklerozan Stromal Tümörü / Sclerosing Stromal Tumor of the Ovary." Osmangazi Journal of Medicine 39, no. 2 (2017): 75–79. http://dx.doi.org/10.20515/otd.330022.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Díaz-Flores, Lucio, Ricardo Gutiérrez, Maria Pino García, et al. "Cd34+ Stromal Cells/Telocytes in Normal and Pathological Skin." International Journal of Molecular Sciences 22, no. 14 (2021): 7342. http://dx.doi.org/10.3390/ijms22147342.

Full text

Abstract:

We studied CD34+ stromal cells/telocytes (CD34+SCs/TCs) in pathologic skin, after briefly examining them in normal conditions. We confirm previous studies by other authors in the normal dermis regarding CD34+SC/TC characteristics and distribution around vessels, nerves and cutaneous annexes, highlighting their practical absence in the papillary dermis and presence in the bulge region of perifollicular groups of very small CD34+ stromal cells. In non-tumoral skin pathology, we studied examples of the principal histologic patterns in which CD34+SCs/TCs have (1) a fundamental pathophysiological r

APA, Harvard, Vancouver, ISO, and other styles

48

Quist, Sven R., Maximilian Eckardt, André Kriesche, and Harald P. Gollnick. "Expression of Potential Dermal Progenitor Cell Markers in the Tumour and Stroma of Skin Adnexal Malignant and Benign Tumours." Stem Cells International 2019 (April 1, 2019): 1–10. http://dx.doi.org/10.1155/2019/9320701.

Full text

Abstract:

Stem cells are multipotent cells that maintain the skin epidermis including skin appendages such as hair follicle, sebaceous glands, and sweat glands. There is evidence that reciprocal signalling between the epidermis and the dermis plays an important role in skin development, homeostasis, wound repair, and skin cancer. The origin of skin cancer that derive from skin appendages is still controversial, including basal cell carcinoma and even more of rare tumours such as sebaceous carcinomas and whether those tumours originate from resident tissue stem cells. To investigate whether markers repor

APA, Harvard, Vancouver, ISO, and other styles

49

Uner, Meral, and Alp Usubutun. "Sclerosing Stromal Tumor Mimicking a Pregnancy Luteoma: Case Report of a Diagnostically Challenging Entity Further Complicated by the Presence of Metastatic Signet Ring Cell Carcinoma From the Stomach." International Journal of Surgical Pathology 25, no. 8 (2017): 739–44. http://dx.doi.org/10.1177/1066896917716303.

Full text

Abstract:

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 immu

APA, Harvard, Vancouver, ISO, and other styles

50

Kadiroğulları, Pınar, and Kerem Doğa Seçkin. "Sclerosing stromal tumor: a rare ovarian neoplasm." Journal of the Turkish-German Gynecological Association 23, no. 1 (2022): 68–70. http://dx.doi.org/10.4274/jtgga.galenos.2021.2021.0097.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!