Immunohistochemistry micrograph of androgen receptors on a HGSC tumour sample
High-grade serous carcinoma (HGSC) is a type of tumour that arises from the serous epithelial layer in the abdominopelvic cavity and is mainly found in the ovary. HGSCs make up the majority of ovarian cancer cases[1] and have the lowest survival rates.[2]
HGSC is distinct from low-grade serous carcinoma (LGSC) which arises from ovarian tissue, is less aggressive and is present in stage I ovarian cancer where tumours are localised to the ovary.
Although originally thought to arise from the squamous epithelial cell layer covering the ovary, HGSC is now thought to originate in the Fallopian tube epithelium. HGSC is much more invasive than LGSC with a higher fatality rate - although it is more sensitive to platinum-based chemotherapy,[3][4] possibly due to its rapid growth rate. In rare cases, HGSCs can develop from LGSCs,[5] but generally the two types arise independently of each other.
^Santillan, A.; Kim, Y.w.; Zahurak, M.l.; Gardner, G.j.; Giuntoli, R.l.; Shih, I.m.; Bristow, R.e. (2007-05-01). "Differences of chemoresistance assay between invasive micropapillary/low-grade serous ovarian carcinoma and high-grade serous ovarian carcinoma". International Journal of Gynecological Cancer. 17 (3): 601–606. doi:10.1111/j.1525-1438.2007.00820.x. ISSN1525-1438. PMID17504374. S2CID21579941.
^Schmeler, Kathleen M.; Sun, Charlotte C.; Bodurka, Diane C.; Deavers, Michael T.; Malpica, Anais; Coleman, Robert L.; Ramirez, Pedro T.; Gershenson, David M. (2008-03-01). "Neoadjuvant chemotherapy for low-grade serous carcinoma of the ovary or peritoneum". Gynecologic Oncology. 108 (3): 510–514. doi:10.1016/j.ygyno.2007.11.013. ISSN1095-6859. PMID18155273.
^Dehari, Reiko; Kurman, Robert J.; Logani, Sanjay; Shih, Ie-Ming (2007-07-01). "The development of high-grade serous carcinoma from atypical proliferative (borderline) serous tumors and low-grade micropapillary serous carcinoma: a morphologic and molecular genetic analysis". The American Journal of Surgical Pathology. 31 (7): 1007–1012. doi:10.1097/PAS.0b013e31802cbbe9. ISSN0147-5185. PMID17592266. S2CID37905442.