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Possible impact of immunosuppressive therapy regimens on histopathologic outcomes of abnormal uterine bleeding in solid-organ transplant recipients
被引:2
|作者:
Tohma, Yusuf Aytac
[1
]
Akilli, Huseyin
[1
]
Kirnap, Mahir
[2
]
Haberal, Asuman Nihan
[3
]
Akyel, Dilan
[4
]
Zengin, Hatice Yagmur
[5
]
Zeyneloglu, Hulusi Bulent
[1
]
Kuscu, Esra
[1
]
Ayhan, Ali
[1
]
Haberal, Mehmet
[2
]
机构:
[1] Baskent Univ, Dept Obstet & Gynecol, Sch Med, Ankara, Turkey
[2] Baskent Univ, Dept Gen Surg, Sch Med, Ankara, Turkey
[3] Baskent Univ, Dept Pathol, Sch Med, Ankara, Turkey
[4] Baskent Univ, Dept Family Med, Sch Med, Ankara, Turkey
[5] Baskent Univ, Dept Biostat, Sch Med, Ankara, Turkey
关键词:
endometrial hyperplasia;
immunosuppressive therapy;
liver transplantation;
renal transplantation;
sirolimus;
DE-NOVO MALIGNANCIES;
ENDOMETRIAL HYPERPLASIA;
KIDNEY-TRANSPLANTATION;
WOMEN;
CYCLOSPORINE;
DRUGS;
D O I:
10.1111/ctr.13305
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
Background: In this study, we aimed to determine the frequency of histopathologic outcomes of solid-organ transplantation in women with abnormal uterine bleeding (AUB) receiving immunosuppressive therapies. Methods: This is a retrospective study including a single-center experience. Data were extracted from hospital records, and solid-organ transplant recipients who were diagnosed with AUB were included. Results: Fifty-five of these patients were renal transplant recipients (79.7%), and 14 were liver transplant recipients (20.3%). Histopathologic examination showed various histopathologic patterns of endometrium in patients with AUB consisting of normal histopathologic findings of endometrium in 31 patients (48.4%); 29 hormonal imbalance during proliferative and secretory phases of menstrual cycle and two atrophic endometrium. Endometrial hyperplasia without atypia was observed in 11 patients (17.2%). Polyp was seen in 22 patients (34.4%); 21 endometrial polyp and one endocervical polyp. There were significant differences in terms of histopathologic findings among the three groups of patients according to different immunosuppressive regimens (P = .029). There was no endometrial hyperplasia in women receiving sirolimus-based immunosuppressive regimens. Moreover, there was no endometrial hyperplasia in the liver transplant recipient group. Conclusions: Sirolimus-based immunosuppressive regimens may be administered to patients who have risk factors for endometrial precancerous lesions, such as endometrial hyperplasia. However, additional well-designed, large-scale studies are warranted to confirm our findings.
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