生殖器模糊——病因、诊断和治疗。

D D Federman, P K Donahoe
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引用次数: 0

摘要

与十年前相比,生殖器模糊的患者有更好的机会接受快速诊断、适当的替代治疗和功能性手术重建。虽然真正雌雄同体和混合性性腺发育不良的病因尚不清楚,但大多数女性假雌雄同体或CAH的基因缺陷已被确定为21-羟化酶基因。不完全男性化被发现是由于雄激素受体,5 α还原酶或从胆固醇到睾酮的途径中的酶的缺陷。SRY点突变与46XY纯性腺发育不良有关。存留的勒氏管归因于MIS基因的点突变;MIS水平正常的人应该有受体缺陷。子宫内诊断和治疗以及着床前阶段的诊断可能对这些患者的护理非常重要,这些患者可能是基因替代治疗的潜在候选者。必要时可进行手术重建。如果孩子是作为女性抚养的,阴蒂收缩、阴唇缩小和突出以及阴道成形术可以在婴儿期早期完成,作为一个广泛的一期手术。如果将患者作为男性抚养,则可以进行各种类型的尿道下裂修复,生殖腺可以用假体代替,阴茎前阴囊可以重建,以保留输精管为目的切除勒管结构。糖皮质激素和矿物皮质激素的替代治疗必须精确管理,以允许适当的生长,并且必须仔细考虑和管理睾酮,雌激素和黄体酮的替代。照顾这些病人的一个最重要的因素是心理支持,首先是家属,然后是病人需要的。这一点必须谨慎地传达。对这些复杂病人的适当护理要求医生既是临床医生又是熟练的技术人员。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ambiguous genitalia--etiology, diagnosis, and therapy.

Patients with ambiguous genitalia stand a far better chance of receiving a rapid diagnosis, appropriate replacement therapy, and functional surgical reconstruction than was the case even a decade ago. Although the etiologies of true hermaphroditism and mixed gonadal dysgenesis remain elusive, most gene defects in female pseudohermaphroditism or CAH have been pinpointed to the 21-hydroxylase gene. Incomplete masculinization has been found to be due to defects in the androgen receptor, 5 alpha-reductase, or enzymes in the pathway from cholesterol to testosterone. SRY point mutations have been implicated in 46XY pure gonadal dysgenesis. Retained müllerian ducts have been attributed to point mutations in the MIS gene; those with normal MIS levels should be expected to have receptor deficits. In utero diagnoses and treatment and diagnosis at the preimplantation stage may prove to be very important for the care of some of these patients, who may be potential candidates for gene replacement therapy. When necessary, surgical reconstruction can be done. If the child is to be raised as a female, clitoral recession, labioscrotal reductions and advancements, and vaginoplasties for exteriorization can be accomplished in early infancy as an extensive one-stage procedure. If patients are to be raised as males, then various types of hypospadias repair can be done, gonads can be replaced with prostheses, the prepenile scrotum can be reconstructed, and müllerian structures can be removed with the goal of preserving the vas deferens. Replacement therapy with glucocorticoids and mineralocorticoids must be precisely managed to permit proper growth, and testosterone, estrogen, and progesterone replacement must be carefully considered and managed. A most important element in the care of these patients is the psychological support that first the families and then the patient require. This must be delivered with sensitivity. The proper care of these complex patients requires that the physician be a scientist as well as a clinician and a skilled technician.

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