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Quoted phrase not found in phrase index: "Juvenile type ovarian granulosa cell tumor"
Page 1
Ovarian sex cord-stromal tumours and their mimics.
Young RH. Young RH. Pathology. 2018 Jan;50(1):5-15. doi: 10.1016/j.pathol.2017.09.007. Epub 2017 Nov 11. Pathology. 2018. PMID: 29132723 Review.
The most common malignant form, the adult granulosa cell tumour, may grossly simulate various surface epithelial neoplasms. ...Thorough sampling generally resolves this differential and if not immunohistochemistry aids. Although the adult granulosa …
The most common malignant form, the adult granulosa cell tumour, may grossly simulate various surface epithelial neo …
Gynecological neoplasms associated with paraneoplastic hypercalcemia.
Lim D, Oliva E. Lim D, et al. Semin Diagn Pathol. 2019 Jul;36(4):246-259. doi: 10.1053/j.semdp.2019.01.003. Epub 2019 Feb 1. Semin Diagn Pathol. 2019. PMID: 30772079 Review.
Approximately 5% of gynecological malignancies are associated with paraneoplastic hypercalcemia. Awareness of its association with certain tumor types allows for earlier disease detection and facilitates monitoring of treatment response and disease recurrence. We review th …
Approximately 5% of gynecological malignancies are associated with paraneoplastic hypercalcemia. Awareness of its association with certain …
Paediatric ovarian tumours and their associated cancer susceptibility syndromes.
Goudie C, Witkowski L, Vairy S, McCluggage WG, Foulkes WD. Goudie C, et al. J Med Genet. 2018 Jan;55(1):1-10. doi: 10.1136/jmedgenet-2017-104926. Epub 2017 Nov 24. J Med Genet. 2018. PMID: 29175835 Review.
Non-epithelial ovarian tumours are rare neoplasms that occasionally arise in childhood and adolescence. ...Specifically, juvenile granulosa cell tumours, Sertoli-Leydig cell tumours, sex cord tumours with annul …
Non-epithelial ovarian tumours are rare neoplasms that occasionally arise in childhood and adolescence. ...Specifically …
Ovarian sex-cord stromal tumours and small cell tumours: Pathological, genetic and management aspects.
Boussios S, Moschetta M, Zarkavelis G, Papadaki A, Kefas A, Tatsi K. Boussios S, et al. Crit Rev Oncol Hematol. 2017 Dec;120:43-51. doi: 10.1016/j.critrevonc.2017.10.007. Epub 2017 Oct 16. Crit Rev Oncol Hematol. 2017. PMID: 29198337 Review.
They include malignancies of germ cell origin, sex cord-stromal cell origin, and a variety of extremely rare ovarian cancers, such as small-cell carcinomas and sarcomas. ...In this article, it is provided an overview of the current knowledge on the inc …
They include malignancies of germ cell origin, sex cord-stromal cell origin, and a variety of extremely rare ovarian ca …
Ovarian tumors: a survey of selected advances of note during the life of this journal.
Young RH. Young RH. Hum Pathol. 2020 Jan;95:169-206. doi: 10.1016/j.humpath.2019.09.002. Epub 2019 Oct 22. Hum Pathol. 2020. PMID: 31654691 Review.
The author reviews highlights of advances in knowledge concerning ovarian tumor pathology since the time of an essay in the first issue of this Journal written by Dr Robert E. ...The current review considers the neoplasms in essentially the same order as was …
The author reviews highlights of advances in knowledge concerning ovarian tumor pathology since the time of an essay in the fi …
Stage I juvenile granulosa cell tumors of the ovary: A multicentre analysis from the MITO-9 study.
Bergamini A, Ferrandina G, Candotti G, Taccagni G, Scarfone G, Bocciolone L, Cassani C, Marinaccio M, Pignata S, Candiani M, Mangili G. Bergamini A, et al. Eur J Surg Oncol. 2021 Jul;47(7):1705-1709. doi: 10.1016/j.ejso.2021.02.003. Epub 2021 Feb 9. Eur J Surg Oncol. 2021. PMID: 33583630
OBJECTIVE: Juvenile type granulosa cell tumor (JGCTs) are extremely rare, mainly diagnosed in young women and pre-pubertal girls at stage I disease. ...The aim of this study is to add on the experience of the MITO group (Multicenter Italian Tria …
OBJECTIVE: Juvenile type granulosa cell tumor (JGCTs) are extremely rare, mainly diagnosed in young women …
Granulosa cell tumor of testis: clinicopathological correlation of a rare tumor.
Rane SU, Menon S, Desai S, Bakshi G, Joshi A. Rane SU, et al. Indian J Pathol Microbiol. 2014 Oct-Dec;57(4):564-73. doi: 10.4103/0377-4929.142665. Indian J Pathol Microbiol. 2014. PMID: 25308008
BACKGROUND: Granulosa cell tumor of testis is a rare tumor accounting for less than 4% of adult testicular tumors though they account for nearly 30% of childhood testicular tumors. ...Morphology and immunohistochemistry were classical in …
BACKGROUND: Granulosa cell tumor of testis is a rare tumor accounting for less than 4% of adult testicular tu …
Detection of FOXL2 C134W Mutation Status by a Novel BaseScope In Situ Hybridization Assay is Highly Sensitive and Specific for Adult Granulosa Cell Tumors.
Hammer PM, Wang A, Beard C, Zdravkovic S, Tenney T, Liang B, Das I, Bremer R, Wang LC, McCluggage WG, Stewart CJR, Howitt BE. Hammer PM, et al. Mod Pathol. 2023 Nov;36(11):100318. doi: 10.1016/j.modpat.2023.100318. Epub 2023 Aug 25. Mod Pathol. 2023. PMID: 37634867
Adult granulosa cell tumors (AGCTs) are a molecularly distinct group of malignant ovarian sex cord-stromal tumors (SCSTs) characterized by a nearly ubiquitous c.402C>G/p.C134W mutation in FOXL2 (hereafter referred to as "C134W"). ...We descri …
Adult granulosa cell tumors (AGCTs) are a molecularly distinct group of malignant ovarian sex cord-stromal tu …
Atypical Presentation of Granulosa Cell Tumor in an Adolescent: A Case Report.
Morrison A, Pressey JG, VandenHeuvel K, Streich-Tilles T. Morrison A, et al. J Pediatr Adolesc Gynecol. 2023 Dec;36(6):553-555. doi: 10.1016/j.jpag.2023.06.007. Epub 2023 Jun 22. J Pediatr Adolesc Gynecol. 2023. PMID: 37354988
BACKGROUND: Granulosa cell tumors (GCTs) frequently present with elevated levels of estrogen and inhibin. Most diagnoses in the pediatric and adolescent population are juvenile-type GCTs; adult-type GCTs in this population are rare. CASE: …
BACKGROUND: Granulosa cell tumors (GCTs) frequently present with elevated levels of estrogen and inhibin. Most diagnose …
Ovarian Granulosa Cell Tumor Initially Presenting as a Giant Liver Mass Radiologically Mimicking Primary Cystic Cholangiocarcinoma.
Qian X, Cong Z, Lai J. Qian X, et al. In Vivo. 2023 Mar-Apr;37(2):734-737. doi: 10.21873/invivo.13135. In Vivo. 2023. PMID: 36881092 Free PMC article.
BACKGROUND: Ovarian granulosa cell tumor (GCT) is a rare type of malignant sex-cord stromal tumor, with adult and juvenile types. ...CONCLUSION: To the best of our knowledge, this is the first documented case of ovarian g …
BACKGROUND: Ovarian granulosa cell tumor (GCT) is a rare type of malignant sex-cord stromal tumor, …
52 results