Rahoui Moez, Ouanes Yassine, Chaker Kays, Bibi Mokhtar, Mourad Daly Kheireddine, Sellami Ahmed, Ben Rhouma Sami, Nouira Yassine
Urology Department La Rabta Hospital, Tunis, Tunisia.
Ann Med Surg (Lond). 2022 Jun 25;79:104068. doi: 10.1016/j.amsu.2022.104068. eCollection 2022 Jul.
and importance: Infertility affects approximately 10-15% of couples worldwide. Several causes are incriminated such as hormonal abnormalities, infections, genetic disorders, testicular cancer, varicocele, and others. Herein, we report a case of an unusual association between testicular tuberculosis and microdeletion of the Y chromosome in an infertile patient and we discuss the diagnostic and therapeutic difficulties.
A 36-year-old patient, a smoker, with no previous history consulted our department for primary infertility for 2 years. The clinical examination was normal. The sperm count showed azoospermia. karyotype analysis confirmed the diagnosis of a microdeletion of the Y chromosome. A testicular biopsy was performed. The microscopic analysis did not find any sperm cells. However, the histopathological examination was in favor of testicular TB. The patient received 6 months of anti-TB treatment. He remained azoospermic.
Azoospermia is defined as the absence of sperm in the ejaculate in two different samples. This condition is classified as obstructive and non-obstructive. The etiology of this condition is either an intrinsic testicular deficiency or an insufficient production of gonadotropins. Genetic and chromosomal abnormalities should be investigated due to the higher incidence in azoospermic patients compared to the normal population. Testicular causes are dominated by infections, trauma, ischemia, and iatrogenic causes such as chemotherapy and radiotherapy. Genetic causes are dominated by Klinefelter syndrome and Y-chromosome microdeletions.
Azoospermia is a frequent cause of male infertility. Several causes are incriminated such as hormonal abnormalities, infections, genetic disorders, and others. In some cases, this condition can be multifactorial.
及重要性:不孕症影响着全球约10%-15%的夫妇。其病因有多种,如激素异常、感染、遗传疾病、睾丸癌、精索静脉曲张等。在此,我们报告一例不育患者中睾丸结核与Y染色体微缺失的罕见关联,并讨论诊断和治疗上的困难。
一名36岁男性患者,有吸烟史,此前无特殊病史,因原发性不孕2年前来我科就诊。临床检查正常。精液分析显示无精子症。核型分析确诊为Y染色体微缺失。进行了睾丸活检。显微镜检查未发现任何精子细胞。然而,组织病理学检查支持睾丸结核的诊断。该患者接受了6个月的抗结核治疗。他仍为无精子症。
无精子症定义为两次不同样本的精液中均无精子。这种情况分为梗阻性和非梗阻性。其病因要么是睾丸内在缺陷,要么是促性腺激素分泌不足。由于无精子症患者的发病率高于正常人群,因此应调查遗传和染色体异常情况。睾丸性病因以感染、创伤、缺血以及化疗和放疗等医源性因素为主。遗传性病因以克兰费尔特综合征和Y染色体微缺失为主。
无精子症是男性不育的常见原因。其病因有多种,如激素异常、感染、遗传疾病等。在某些情况下,这种情况可能是多因素的。