Endometrioid Borderline Ovarian Tumor: Clinical Characteristics, Prognosis, and Managements.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 12 01 2022
accepted: 27 04 2022
pubmed: 20 5 2022
medline: 11 8 2022
entrez: 19 5 2022
Statut: ppublish

Résumé

Endometrioid borderline ovarian tumor (EBOT) is a rare subtype of borderline ovarian malignancies. This study was designed to determine the prognosis of a series of EBOT. This is a retrospective review of patients with EBOT treated in or referred to our institutions and a centralized, histological review by a reference pathologist. Data on the clinical characteristics, management (surgical and medical), and oncologic outcomes of patients were required for inclusion. Forty-eight patients were identified. Median age was 52 years (range 14-89). Fourteen patients underwent a conservative surgery and 32 a bilateral salpingo-oophorectomy (unknown in 2 cases). Two patients had bilateral tumors. Forty-three patients had stage I disease, and five patients had stage II disease (10%). Stromal microinvasion and intraepithelial carcinoma was observed in 6 (12%) and 13 (27%) patients respectively. Endometriosis was histologically associated in 12 patients (25%). Synchronous endometrial disease was found in 7 (24%) of 29 patients with endometrial histological evaluation. The median follow-up was 72 months (range 6-146). Two patients developed a recurrence after cystectomy in form of borderline disease (5%). No death related to EBOT occurred. Peritoneal restaging surgery should be performed if not realized initially, because 5% of EBOTS are diagnosed at stage II-III. Fertility-sparing surgery seems a safe option in selected patients. Because synchronous endometrial diseases, including endometrial carcinoma are frequent, systematic hysterectomy (or endometrial sampling in case of fertility-sparing surgery) is mandatory. Prognosis is generally excellent. Recurrence is a rare event (6%), but it can occur in the form of invasive disease.

Sections du résumé

BACKGROUND BACKGROUND
Endometrioid borderline ovarian tumor (EBOT) is a rare subtype of borderline ovarian malignancies. This study was designed to determine the prognosis of a series of EBOT.
METHODS METHODS
This is a retrospective review of patients with EBOT treated in or referred to our institutions and a centralized, histological review by a reference pathologist. Data on the clinical characteristics, management (surgical and medical), and oncologic outcomes of patients were required for inclusion.
RESULTS RESULTS
Forty-eight patients were identified. Median age was 52 years (range 14-89). Fourteen patients underwent a conservative surgery and 32 a bilateral salpingo-oophorectomy (unknown in 2 cases). Two patients had bilateral tumors. Forty-three patients had stage I disease, and five patients had stage II disease (10%). Stromal microinvasion and intraepithelial carcinoma was observed in 6 (12%) and 13 (27%) patients respectively. Endometriosis was histologically associated in 12 patients (25%). Synchronous endometrial disease was found in 7 (24%) of 29 patients with endometrial histological evaluation. The median follow-up was 72 months (range 6-146). Two patients developed a recurrence after cystectomy in form of borderline disease (5%). No death related to EBOT occurred.
CONCLUSIONS CONCLUSIONS
Peritoneal restaging surgery should be performed if not realized initially, because 5% of EBOTS are diagnosed at stage II-III. Fertility-sparing surgery seems a safe option in selected patients. Because synchronous endometrial diseases, including endometrial carcinoma are frequent, systematic hysterectomy (or endometrial sampling in case of fertility-sparing surgery) is mandatory. Prognosis is generally excellent. Recurrence is a rare event (6%), but it can occur in the form of invasive disease.

Identifiants

pubmed: 35590116
doi: 10.1245/s10434-022-11893-7
pii: 10.1245/s10434-022-11893-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5894-5903

Informations de copyright

© 2022. Society of Surgical Oncology.

Références

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Auteurs

Giulio Ricotta (G)

Department of Gynaecologic Surgery, Gustave-Roussy, Villejuif, France.

Amandine Maulard (A)

Department of Gynaecologic Surgery, Gustave-Roussy, Villejuif, France.

Massimo Candiani (M)

IRCCS San Raffaele Hospital, Vita-Salute University, Milan, Italy.

Stephanie Scherrier (S)

Department of Gynaecologic Surgery, Gustave-Roussy, Villejuif, France.

Catherine Genestie (C)

Department of Pathology, Gustave-Roussy, Villejuif, France.

Patricia Pautier (P)

Department of Medical Oncology, Gustave-Roussy, Villejuif, France.

Alexandra Leary (A)

Department of Medical Oncology, Gustave-Roussy, Villejuif, France.

Cyrus Chargari (C)

Department of Radiation Oncology, Gustave-Roussy, Villejuif, France.

Giorgia Mangili (G)

IRCCS San Raffaele Hospital, Vita-Salute University, Milan, Italy.

Philippe Morice (P)

Department of Gynaecologic Surgery, Gustave-Roussy, Villejuif, France. Philippe.MORICE@gustaveroussy.fr.
Paris Sud University Kremlin-Bicêtre, Le Kremlin-Bicêtre, France. Philippe.MORICE@gustaveroussy.fr.

Sébastien Gouy (S)

Department of Gynaecologic Surgery, Gustave-Roussy, Villejuif, France.

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