Hematospermia in a Transgender Woman with Evidence for Endometrial Tissue in the Prostate

Q3 Medicine
Janet Coleman-Belin BS , Uchechukwu O. Amakiri BS , Fang-Ming Deng MD, PhD , Deepthi Hoskoppal MD , Joshua D. Safer MD , Tamar Reisman MD
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引用次数: 0

Abstract

Background/Objective

The frequency of hematospermia in transgender women is unknown. This report aimed to describe the development of hematospermia in a transgender woman.

Case Report

A 35-year-old transgender woman treated with estradiol valerate and leuprolide presented with painless rust-tinged ejaculate, urethral bleeding after ejaculation, and intermittent hematuria. Her medical history included gastroesophageal reflux disease, internal hemorrhoids, and attention deficit hyperactivity disorder with negative tobacco smoking and urologic history. Additional medications included emtricitabine-tenofovir disoproxil fumarate and fexofenadine. Physical examination did not reveal constitutional or genitourinary abnormalities. Urinalysis and culture disclosed rare white blood cells with gram-variable bacilli. The chlamydia, gonorrhea, and human immunodeficiency virus test results were negative. Abdominal computed tomography did not reveal bladder or prostate cancer, calcifications, inflammation, or cysts. She continued to have symptoms after this initial workup. One year after the initial symptom onset, transrectal ultrasound disclosed a 1.7-cm midline posterior prostatic cyst with hemorrhagic products, later revealed by magnetic resonance imaging as communicating with the left seminal vesicle. Two ultrasound-guided transperineal biopsy samples revealed benign prostatic tissue with a small focus of Müllerian or endometrial-type tissue, evidenced by immunopositivity for paired-box gene 8 and estrogen receptor in epithelium and cluster of differentiation 10 immunopositivity in stroma. After medical consultation, the patient underwent prostatic cyst aspiration, resection of the transurethral ejaculatory ducts, and orchiectomy. She did not experience any complications after these procedures.

Discussion

The etiology of hematospermia may be idiopathic, iatrogenic, anatomic, or pathologic.

Conclusion

Occult endometriosis or ectopic Müllerian epithelial tissue growth may occur in transgender women taking feminizing gender-affirming hormone therapy.

一名变性女性的血精症与前列腺中子宫内膜组织的证据
背景/目的变性女性发生血精症的频率尚不清楚。病例报告 一位 35 岁的变性女性在接受戊酸雌二醇和亮丙瑞林治疗后出现无痛铁锈色射精、射精后尿道出血和间歇性血尿。她的病史包括胃食管反流病、内痔和注意力缺陷多动障碍,吸烟史和泌尿科病史均为阴性。其他药物包括富马酸恩曲他滨-替诺福韦二吡呋酯和非索非那定。体格检查未发现体质或泌尿生殖系统异常。尿液分析和培养结果显示,罕见白细胞中含有革兰氏变异杆菌。衣原体、淋病和人类免疫缺陷病毒检测结果均为阴性。腹部计算机断层扫描未发现膀胱癌或前列腺癌、钙化、炎症或囊肿。初次检查后,她继续出现症状。最初出现症状一年后,经直肠超声检查发现了一个 1.7 厘米的中线后前列腺囊肿,囊肿内有出血产物,后来经磁共振成像检查发现囊肿与左侧精囊相通。两份超声引导下的经会阴活检样本显示为良性前列腺组织,其中有一小灶为穆勒氏组织或子宫内膜型组织,上皮中的配对盒基因8和雌激素受体免疫阳性,基质中的分化簇10免疫阳性。经医生会诊后,患者接受了前列腺囊肿抽吸术、经尿道射精管切除术和睾丸切除术。讨论血精症的病因可能是特发性的、先天性的、解剖学的或病理学的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
AACE Clinical Case Reports
AACE Clinical Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.30
自引率
0.00%
发文量
61
审稿时长
55 days
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