Uterine Tumors Resembling Ovarian Sex Cord Tumors (UTROSCTs): A Scoping Review of 511 Cases, Including 2 New Cases

被引:6
|
作者
Watrowski, Rafal [1 ,2 ]
Palumbo, Mario [3 ]
Guerra, Serena [3 ]
Gallo, Alessandra [3 ]
Zizolfi, Brunella [3 ]
Giampaolino, Pierluigi [3 ]
Bifulco, Giuseppe [3 ]
Sardo, Attilio Di Spiezio [3 ]
De Angelis, Maria Chiara [3 ]
机构
[1] Helios Hosp Mullheim, Dept Obstet & Gynecol, D-79379 Mullheim, Germany
[2] Univ Freiburg, Fac Med, D-79106 Freiburg, Germany
[3] Univ Naples Federico II, Sch Med, Dept Publ Hlth, I-80138 Naples, Italy
来源
MEDICINA-LITHUANIA | 2024年 / 60卷 / 01期
关键词
Uterine Tumor Resembling Ovarian Sex Cord Tumor (UTROSCT); hysteroscopy; hysterectomy; fertility-sparing; gene fusions; low malignant potential; STROMAL TUMOR; CLINICOPATHOLOGICAL FEATURES; CLINICAL CHARACTERISTICS; CONSERVATIVE-MANAGEMENT; ENDOMETRIAL; RARE; NEOPLASM; DIFFERENTIATION; STROMOMYOMA; RECURRENCE;
D O I
10.3390/medicina60010179
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Uterine Tumors Resembling Ovarian Sex Cord Tumors (UTROSCTs) are rare uterine mesenchymal neoplasms with uncertain biological potential. These tumors, which affect both premenopausal and postmenopausal women, usually have a benign clinical course. Nevertheless, local recurrences and distant metastases have been described. By analyzing 511 cases retrieved from individual reports and cases series, we provide here the most comprehensive overview of UTROSCT cases available in the literature, supplemented by two new cases of UTROSCTs. Case 1 was an asymptomatic 31-year-old woman who underwent a laparoscopic resection of a presumed leiomyoma. Case 2 was a 58-year-old postmenopausal woman with abnormal vaginal bleeding who underwent an outpatient hysteroscopic biopsy of a suspicious endometrial area. In both cases, immunohistochemical positivity for Calretinin and Inhibin was noted, typical for a sex cord differentiation. In both cases, total laparoscopic hysterectomy with bilateral salpingo-oophorectomy was performed. In light of the available literature, no pathognomonic clinical or imaging finding can be attributed to UTROSCT. Patients usually present with abnormal uterine bleeding or pelvic discomfort, but 20% of them are asymptomatic. In most cases, a simple hysterectomy appears to be the appropriate treatment, but for women who wish to become pregnant, uterus-preserving approaches should be discussed after excluding risk factors. Age, tumor size, lymphovascular space invasion, nuclear atypia, and cervical involvement are not reliable prognostic factors in UTROSCT. The current research suggests that aggressive cases (with extrauterine spread or recurrence) can be identified based on a distinct genetic and immunohistochemical phenotype. For instance, UTROSCTs characterized by GREB1::NCOA1-3 fusions and PD-L1 molecule expression appear to be predisposed to more aggressive behaviors and recurrence, with GREB1::NCOA2 being the most common gene fusion in recurrent tumors. Hence, redefining the criteria for UTROSCTs may allow a better selection of women suitable for fertility-sparing treatments or requiring more aggressive treatments in the future.
引用
收藏
页数:35
相关论文
共 43 条
  • [1] Clinicopathological features of two cases of uterine tumors resembling ovarian sex-cord tumors (UTROSCTs) and a comprehensive review of literature
    Viau, M.
    Grondin, K.
    Gregoire, J.
    Renaud, M. C.
    Plante, M.
    Sebastianelli, A.
    EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY, 2017, 38 (05) : 793 - 799
  • [2] Uterine Tumors Resembling Ovarian Sex Cord Tumors: An Ultrastructural Analysis of 13 Cases
    Gupta, Mamta
    de Leval, Laurence
    Selig, Martin
    Oliva, Esther
    Nielsen, G. Petur
    ULTRASTRUCTURAL PATHOLOGY, 2010, 34 (01) : 16 - 24
  • [3] Uterine tumors resembling ovarian sex cord-stromal tumors: synchronous uterine tumors resembling ovarian sex cord-stromal tumors and ovarian sex cord tumor
    Abdullazade, Samir
    Kosemehmetoglu, Kemal
    Adanir, Ilknur
    Kutluay, Lale
    Usubutun, Alp
    ANNALS OF DIAGNOSTIC PATHOLOGY, 2010, 14 (06) : 432 - 437
  • [4] Uterine Tumors Resembling Ovarian Sex Cord Tumors Identified at Resectoscopic Endometrial Ablation: Report of 2 Cases
    Vilos, Angelos G.
    Zhu, Cici
    Abu-Rafea, Basim
    Ettler, Helen C.
    Weir, Michele M.
    Vilos, George A.
    JOURNAL OF MINIMALLY INVASIVE GYNECOLOGY, 2019, 26 (01) : 105 - 109
  • [5] Uterine tumors resembling ovarian sex cord tumors (UTROSCT) with metastasis: clinicopathological study of two cases
    Umeda, Shigeaki
    Tateno, Masatoshi
    Miyagi, Etsuko
    Sakurai, Koji
    Tanaka, Reiko
    Tateishi, Yoko
    Tokinaga, Aya
    Ohashi, Kenichi
    Furuya, Mitsuko
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2014, 7 (03): : 1051 - 1059
  • [6] Clinical experience of uterine tumors resembling ovarian sex cord tumors: a clinicopathological analysis of 6 cases
    Liu, Cai-Yan
    Shen, Yan
    Zhao, Jian-Guo
    Qu, Peng-Peng
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, 2015, 8 (04): : 4158 - 4164
  • [7] Diverse Phenotypic Profile of Uterine Tumors Resembling Ovarian Sex Cord Tumors An Immunohistochemical Study of 12 Cases
    de Leval, Laurence
    Lim, Gkeok Stzuan Diana
    Waltregny, David
    Oliva, Esther
    AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2010, 34 (12) : 1749 - 1761
  • [8] Uterine Tumor Resembling Ovarian Sex Cord Tumors Treated by Resectoscopic Surgery
    Garuti, Giancarlo
    Gonfiantini, Cristina
    Mirra, Maurizio
    Galli, Carlo
    Luerti, Massimo
    JOURNAL OF MINIMALLY INVASIVE GYNECOLOGY, 2009, 16 (02) : 236 - 240
  • [9] Uterine tumors resembling ovarian sex cord tumors. A case report
    Carta, G.
    Crisman, G.
    Margiotta, G.
    Mastrocola, N.
    Di Fonso, A.
    Coletti, G.
    EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY, 2010, 31 (04) : 456 - 458
  • [10] FOXL2 Mutation is Absent in Uterine Tumors Resembling Ovarian Sex Cord Tumors
    Chiang, Sarah
    Staats, Paul N.
    Senz, Janine
    Kommoss, Friedrich
    De Nictolis, Michele
    Huntsman, David G.
    Gilks, C. Blake
    Oliva, Esther
    AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2015, 39 (05) : 618 - 623