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混合性性腺发育不全综合征中睾丸及条索状性腺发育异常:来自21例临床病理分析的观点

Dysgenesis of testicular and streak gonads in the syndrome of mixed gonadal dysgenesis: perspective derived from a clinicopathologic analysis of twenty-one cases.

作者信息

Robboy S J, Miller T, Donahoe P K, Jahre C, Welch W R, Haseltine F P, Miller W A, Atkins L, Crawford J D

出版信息

Hum Pathol. 1982 Aug;13(8):700-16. doi: 10.1016/s0046-8177(82)80292-x.

Abstract

The clinical and pathologic aspects of 21 cases of mixed gonadal dysgenesis (MGD) were studied. The gonads in 15 patients consisted of a macroscopic testis and a streak gonad; six patients had variants, including two with bilateral testes and four with bilateral streak gonads or tumors. Functionally, the gonads were incompetent. Testes 1) failed to completely inhibit müllerian development, 2) failed to support full differentiation of mesonephric duct structures, 3) failed to adequately masculinize development of the external genitalia, or 4) often failed to mediate their own descent, resulting in asymmetry of the internal and external genitalia. None of the streak gonads mediated normal female adolescent development or fertility. Microscopic examination revealed that every gonad, regardless of its gross appearance, was morphologically abnormal. Although gonads with seminiferous tubules usually developed to a moderately advanced state, macroscopically resembling testes, the hilar zone remained architecturally disorganized; the cortex invariably lacked more than a rudimentary tunica albuginea or exhibited partial ovarian differentiation, sometimes even with a rare primordial follicle. Over time, the seminiferous tubules atrophied and hyalinized. Gonads that grossly resembled streak gonads were observed microscopically to be composed of a stroma resembling that of normal ovarian cortex. In patients more than several years of age, the entire complement of germ cells in streak gonads disappeared. It is suggested that patients with MGD be raised as females. Early removal of gonads will prevent the development of gonadoblastoma and dysgerminoma. If the uterus is retained and the patient is subsequently given exogenous estrogen, care should be taken to detect early any signs of the development of endometrial carcinoma or its precursor, to which these patients may be prone.

摘要

对21例混合性性腺发育不全(MGD)患者的临床和病理特征进行了研究。15例患者的性腺由一个肉眼可见的睾丸和一条条索状性腺组成;6例患者有变异情况,包括2例双侧睾丸以及4例双侧条索状性腺或肿瘤。从功能上来说,这些性腺功能不全。睾丸1)未能完全抑制苗勒管发育,2)未能支持中肾管结构的充分分化,3)未能充分使外生殖器男性化发育,或者4)常常未能引导自身下降,导致内外生殖器不对称。所有条索状性腺均未介导正常的女性青春期发育或生育功能。显微镜检查显示,每个性腺,无论其大体外观如何,在形态学上均异常。尽管具有生精小管的性腺通常发育到中等程度的成熟状态,肉眼上类似睾丸,但肾门区在结构上仍紊乱;皮质始终缺乏完整的白膜或仅表现出部分卵巢分化,有时甚至有罕见的原始卵泡。随着时间推移,生精小管萎缩并玻璃样变。肉眼上类似条索状性腺的性腺在显微镜下观察由类似于正常卵巢皮质的间质组成。在年龄超过几岁的患者中,条索状性腺中的所有生殖细胞均消失。建议将MGD患者按女性抚养。早期切除性腺可预防性腺母细胞瘤和无性细胞瘤的发生。如果保留子宫且随后给予患者外源性雌激素,应注意尽早发现子宫内膜癌或其前驱病变的任何早期迹象,这些患者可能易患此类疾病。

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