Pérez-Gutiérrez José F, Monteagudo Luís V, Rodríguez-Bertos Antonio, García-Pérez Enrique, Sánchez-Calabuig María J, García-Botey Concepción, Whyte Ana, de la Muela Mercedes Sánchez
From the Departamento de Medicina y Cirugía Animal, Hospital Clínico Veterinario, Facultad de Veterinaria, Universidad Complutense de Madrid, Madrid, Spain (J.P-G, A.R-B, E.G-P, M.S-C, C.G-B, M.SdlM); and Departamento de Anatomía, Embriología y Genética (L.M.) and Departamento de Patología Animal, Facultad de Veterinaria, Universidad de Zaragoza, Zaragoza, Spain (A.W.).
J Am Anim Hosp Assoc. 2015 Jul-Aug;51(4):267-71. doi: 10.5326/JAAHA-MS-6164. Epub 2015 Jun 17.
This report describes a disorder of the sexual development in a beagle dog resulting in an intersex condition. A 6 mo old beagle was presented for evaluation of a protruding structure from the vulva consistent with an enlarged clitoris. Ultrasonographic examination revealed the presence of both gonadal and uterine structures. Retrograde cystourethrovaginogram showed the presence of an os clitoris and severe vaginal stenosis. Histological studies revealed the presence of bilateral ovotestes and uterus. The gonad had interstitial cells within seminiferous-like tubules lined only with Sertoli cells and abundant interstitial cells among primordial, primary, and secondary follicles. Hormone assays completed before and after gonadohysterectomy showed an elevation in the levels of progesterone and dihydrotestosterone that returned to baseline 3 mo after surgery. Testosterone levels that were within the male reference ranges before surgery decreased to basal levels postsurgically. 17-β-Estradiol levels showed little variation and values were always within the reference ranges for a male. Cytogenetic analysis showed a normal female karyotype (2n = 78, XX) and polymerase chain reaction analysis revealed the absence of the sex-determining region Y gene. In summary, the dog presented bilateral ovotestes and a 2n = 78, XX chromosomal complement lacking the sex determining region Y gene, consistent with a diagnosis of true hermaphroditism.
本报告描述了一只比格犬的性发育障碍,导致出现雌雄同体的情况。一只6月龄的比格犬因外阴部有一突出结构前来评估,该结构与增大的阴蒂相符。超声检查显示存在性腺和子宫结构。逆行膀胱尿道阴道造影显示有阴蒂骨和严重的阴道狭窄。组织学研究显示存在双侧卵睾和子宫。性腺在仅由支持细胞衬里的生精样小管内有间质细胞,在原始卵泡、初级卵泡和次级卵泡之间有丰富的间质细胞。性腺子宫切除术前和术后完成的激素测定显示,孕酮和双氢睾酮水平升高,术后3个月恢复至基线水平。术前处于男性参考范围内的睾酮水平术后降至基础水平。17-β-雌二醇水平变化不大,其值始终在男性参考范围内。细胞遗传学分析显示为正常雌性核型(2n = 78, XX),聚合酶链反应分析显示不存在Y染色体性别决定区基因。总之,这只犬表现为双侧卵睾和2n =