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[Clinicopathological features and prognostic analysis of synchronous mucinous metaplasia and neoplasia of the female genital tract].
Lu, L H; Chen, Y Q; Li, J; Shao, S S; Ma, F H; Ning, Y; Shi, Y; Wang, C.
Afiliación
  • Lu LH; Department of Pathology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 2000090, China.
  • Chen YQ; School of Clinical Medicine, Shanghai Medical College, Fudan University, Shanghai 200032, China.
  • Li J; Department of Pathology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 2000090, China.
  • Shao SS; School of Clinical Medicine, Shanghai Medical College, Fudan University, Shanghai 200032, China.
  • Ma FH; Department of Radiology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 200090, China.
  • Ning Y; Department of Pathology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 2000090, China.
  • Shi Y; Department of Gynaecology and Obstetrics, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 200090, China.
  • Wang C; Department of Gynecological Oncology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 200090, China.
Zhonghua Zhong Liu Za Zhi ; 46: 1-14, 2024 Jul 30.
Article en Zh | MEDLINE | ID: mdl-39077828
ABSTRACT

Objective:

Synchronous mucinous metaplasia and neoplasia of the female genital tract (SMMN-FGT) occurring at multiple sites during the same period of time is extremely rare, and the aim of this study was to investigate the clinicopathologic features of SMMN-FGT and its relationship with prognosis.

Methods:

We retrospectively analyzed the clinicopathological features and follow-up records of 25 cases of SMMN-FGT diagnosed from January 2012 to October 2022 in the case database of Obstetrics and Gynecology Hospital of Fudan University.

Results:

The mean and median age at onset were 47 and 46 years old, respectively. Clinical manifestations included irregular vaginal bleeding or drainage, pelvic pain, and ovarian cysts, etc. Germline genetic test confirmed Peutz-Jeghers syndrome (P-J syndrome) in two patients. All patients underwent surgery, and some had postoperative adjuvant radiotherapy and/or chemotherapy. The most frequent site of lesion was the cervix (21 cases), with 11, 10 and 16 cases occurring in the endometrium, fallopian tubes and ovaries, respectively. Six cases involved three sites simultaneously, and only one case had all four sites involved at the same time. Among the 9 cases with P53 mutation phenotype, 6 cases had gastric-type mucinous adenocarcinoma, 2 cases had lobular endocervical glandular hyperplasia, and 1 case had mucinous adenocarcinoma, whereas all the minimally deviated adenocarcinomas had wild phenotype of P53. The median follow-up time was 59 months, during which 3 cases died and 6 cases developed local recurrence or distant metastasis. According to our analysis, postoperative recurrence or metastasis was correlated with the FIGO stage of the disease, the number of lesion sites and the severe degree of the uterine lesions (P<0.05).

Conclusions:

SMMN-FGT had a relatively good clinical prognosis, and even advanced patients could benefit from surgery and adjuvant therapy. In young patients, the ovaries may be preserved if no evidence of lesions were seen after adequate evaluation. In SMMN-FGT, gastric-type mucinous adenocarcinoma occurring in the cervix may have a better prognosis than gastric-type mucinous adenocarcinoma of the cervix alone, so the accurate diagnosis of SMMN-FGT is critical for clinical management.

Texto completo: 1 Base de datos: MEDLINE Idioma: Zh Revista: Zhonghua Zhong Liu Za Zhi Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: Zh Revista: Zhonghua Zhong Liu Za Zhi Año: 2024 Tipo del documento: Article