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Clinical Approach to Neuroendocrine Neoplasm Associated With Ovarian Teratoma.

Authors :
Opalińska M
Sowa-Staszczak A
Olearska H
Ulatowska-Bialas M
Gilis-Januszewska A
Hubalewska-Dydejczyk A
Source :
Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2021 Nov 30; Vol. 12, pp. 770266. Date of Electronic Publication: 2021 Nov 30 (Print Publication: 2021).
Publication Year :
2021

Abstract

Background: Neuroendocrine neoplasms are a heterogeneous group of cancers that develop from enterochromaffin cells of the diffuse endocrine system, with an increase in incidents over the last years. Ovarian neuroendocrine tumors (NET) are rare neoplasms, comprising 0.1% of all ovarian neoplasms and less than 5% of all neuroendocrine tumors. They may arise alone (as monodermal, specialized teratoma - ovarian carcinoid) or as a part of other ovarian lesion: cystic mature or immature teratomas. Due to the rarity and limited amount of such cases reported in the literature, there is no consensus on diagnostic and therapeutic procedures in this group of patients.<br />Materials and Methods: The group of 10 patients at the age of 19 to 77 years (mean 42.8 ± 17.9), diagnosed with unilateral NET within ovarian teratoma were analyzed. The histopathological type of tumor, progression free survival after surgical treatment and presence of hormonally active syndrome were assessed.<br />Results: 70% (n=7) of patients was diagnosed with mature cystic teratomas containing NET component and 30% (n=3) with monodermal teratoma (strumal carcinoid). All cases of monodermal teratomas were found in women at premenopausal age. Determined Ki67 ranged from 2% to 9%. Ninety percent of lesions (n=9) stained positive for synaptophysin and chromogranin, while markers: CK20, CK7, TTF-1 and CDX2 were negative in all cases, which ruled out their metastatic nature. None of the patients presented with carcinoid syndrome. All followed-up patients remain progression-free, which confirms surgical intervention being a crucial and sufficient method of treatment.<br />Conclusions: The prognosis and clinical behavior of NETs associated with ovarian teratomas are good with long progression-free survival.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest<br /> (Copyright © 2021 Opalińska, Sowa-Staszczak, Olearska, Ulatowska-Bialas, Gilis-Januszewska and Hubalewska-Dydejczyk.)

Details

Language :
English
ISSN :
1664-2392
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in endocrinology
Publication Type :
Academic Journal
Accession number :
34917031
Full Text :
https://doi.org/10.3389/fendo.2021.770266