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睾丸支持细胞瘤伴无精子症:一例报告及文献复习

Leydig cell tumor of a testis with azoospermia: A case report and literature review.

作者信息

Kong Qingkuo, Yu Yang, Tian Tian, Zhang Hongguo, Sun Meiling, Liu Ruizhi, Liu Yanhong

机构信息

Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, Jilin 130021, PR China.

出版信息

Medicine (Baltimore). 2020 Sep 4;99(36):e22085. doi: 10.1097/MD.0000000000022085.

DOI:10.1097/MD.0000000000022085
PMID:32899084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7478542/
Abstract

RATIONALE

Testicular tumors represent 1% to 1.5% of all tumors in men. Those derived from Leydig cells are rare and account for 1% of testicular tumors. Leydig tumor cells can produce steroid hormones such as estrogen, progesterone and testosterone. The amount and type of hormones secreted by these tumors may produce complicated clinical characteristics in these patients.

PATIENT CONCERNS

Here, we report a patient with azoospermia, a testicular Leydig cell tumor (LCT), and elevated plasma testosterone levels. We describe the diagnostic and therapeutic experience of this case, and our follow-up of the patient's clinical indicators and fertility status.

DIAGNOSIS

The patient was diagnosed with azoospermia and a testicular LCT.

INTERVENTIONS

The patient underwent testicular tumor removal and long-term follow-up.

OUTCOMES

After 4 months of follow-up, the patient's semen examination index significantly improved and his wife became naturally pregnant. At 4 months of gestation, the fetus was delivered because of a ruptured amniotic cavity. Twenty-six months after tumor removal, the patient's sex hormone levels had completely returned to normal and spermatogenic function had partially recovered, but there was no natural pregnancy with his partner.

CONCLUSION

For LCTs, testis sparing surgery may provide a safe and feasible option to restore spermatogenic function, although longer-term follow-up is required. Drug assistance may be required to maintain spermatogenic function and achieve fertility, and further research is required.

摘要

理论依据

睾丸肿瘤占男性所有肿瘤的1%至1.5%。源自睾丸间质细胞的肿瘤较为罕见,占睾丸肿瘤的1%。睾丸间质细胞瘤细胞可产生雌激素、孕激素和睾酮等甾体激素。这些肿瘤分泌的激素量和类型可能会使这些患者产生复杂的临床特征。

患者情况

在此,我们报告一名患有无精子症、睾丸间质细胞瘤(LCT)且血浆睾酮水平升高的患者。我们描述了该病例的诊断和治疗经验,以及对患者临床指标和生育状况的随访情况。

诊断

该患者被诊断为无精子症和睾丸LCT。

干预措施

患者接受了睾丸肿瘤切除及长期随访。

结果

随访4个月后,患者的精液检查指标显著改善,其妻子自然受孕。妊娠4个月时,因羊膜腔破裂导致胎儿娩出。肿瘤切除26个月后,患者的性激素水平已完全恢复正常,生精功能部分恢复,但与伴侣未自然受孕。

结论

对于LCT,保留睾丸手术可能为恢复生精功能提供一种安全可行的选择,尽管需要更长时间的随访。可能需要药物辅助来维持生精功能并实现生育,这还需要进一步研究。

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Combination treatment of cordycepin and radiation induces MA-10 mouse Leydig tumor cell death via ROS accumulation and DNA damage.虫草素与辐射联合治疗通过活性氧积累和DNA损伤诱导MA-10小鼠睾丸间质细胞瘤细胞死亡。
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Simultaneous Sertoli Cell-Only Syndrome and Leydig Cell Tumor in a Patient with Azoospermia: A Rare Case Report.无精子症患者同时患有唯支持细胞综合征和睾丸间质细胞瘤:一例罕见病例报告
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Leydig cell tumor of the testis, presenting with azoospermia.睾丸间质细胞瘤,表现为无精子症。
Reprod Med Biol. 2017 Jul 20;16(4):392-395. doi: 10.1002/rmb2.12046. eCollection 2017 Oct.
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Long-term follow-up using testicle-sparing surgery for Leydig cell tumor.采用保留睾丸的手术治疗莱迪希细胞瘤的长期随访。
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Leydig cell tumour of the testis: presentation, therapy, long-term follow-up and the role of organ-sparing surgery in a single-institution experience.睾丸间质细胞瘤:单机构经验中的临床表现、治疗、长期随访及保留器官手术的作用
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