A Testicular Leydig Cell Tumor; An Uncommon Cause of Precocious Puberty: A Case Report With Secondary Central Precocious Puberty

Q3 Medicine Acta medica Iranica Pub Date : 2023-04-24 DOI:10.18502/acta.v61i2.12558
Seyede Tahereh Mousavi, Farshad Zohrabi, M. Farzaneh
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Abstract

Sexual precocity in boys is defined as any sign of secondary sexual characteristics present before the age of 9. Leydig cell tumors of the testes are a rare cause of peripheral precocious puberty in boys. Here, we report 8 years and 4-month-old boys with signs of peripheral precocious puberty because of a testicular Leydig cell tumor that developed true precocious puberty after surgical removal. Examination of genitalia showed Tanner 4 hair growth. The penis length was 14.5 cm with a 2.5 cm width. The right testis was enlarged but the left testis was measured at 2cm in length and 1 cm in width. Laboratory results showed low serum gonadotropin levels and increased androgen levels. Testicular sonography reported one solid mass measured 31×28×15 millimeters. With a presumptive diagnosis of Leydig cell tumor, the patient underwent radical orchiectomy. Pathologic evaluation confirmed it. Two months after surgery, the diagnosis of central precocious puberty was confirmed according to physical examination and rising of serum gonadotropins. We started treatment with a Gonadotropin-releasing hormone (GnRH) agonist. Leydig cell tumor in children is an uncommon cause of precocious puberty. In every boy with the sign of peripheral precocious puberty and asymmetrical testicular enlargement, the testicular tumor should be considered. It may induce central precocious puberty after surgical resection and this diagnosis should be considered in the patient’s follow-up in the next visits.
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1例睾丸间质细胞瘤;性早熟的罕见病因:继发性中枢性性早熟1例报告
男孩的性早熟被定义为在9岁之前出现第二性征的任何迹象。睾丸间质细胞瘤是男孩性早熟的罕见病因。在此,我们报告了一例8岁4个月大的男孩,由于睾丸间质细胞肿瘤在手术切除后发展为真正的性早熟,导致周围性性早熟的症状。生殖器检查显示有褐毛生长。阴茎长14.5厘米,宽2.5厘米。右睾丸增大,左睾丸长2cm,宽1cm。实验室结果显示血清促性腺激素水平低,雄激素水平升高。睾丸超声报告一个固体肿块,测量为31×28×15毫米。假定诊断为间质细胞瘤,患者行根治性睾丸切除术。病理检查证实了这一点。术后2个月,体检及血清促性腺激素升高,确诊为中枢性性早熟。我们开始使用促性腺激素释放激素(GnRH)激动剂治疗。儿童间质细胞瘤是引起性早熟的罕见原因。凡是有外周性早熟及不对称睾丸肿大征的男孩,均应考虑睾丸肿瘤。手术切除后可能诱发中枢性性早熟,在患者下次随访时应考虑这一诊断。
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来源期刊
Acta medica Iranica
Acta medica Iranica Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
83
审稿时长
18 weeks
期刊介绍: ACTA MEDICA IRANICA (p. ISSN 0044-6025; e. ISSN: 1735-9694) is the official journal of the Faculty of Medicine, Tehran University of Medical Sciences. The journal is the oldest scientific medical journal of the country, which has been published from 1960 onward in English language. Although it had been published quarterly in the past, the journal has been published bimonthly (6 issues per year) from the year 2004. Acta Medica Iranica it is an international journal with multidisciplinary scope which publishes original research papers, review articles, case reports, and letters to the editor from all over the world. The journal has a wide scope and allows scientists, clinicians, and academic members to publish their original works in this field.
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