Penn State College of Medicine, Hershey, PA, 17033, USA.
Albany Medical Center, Albany, NY 12208, USA.
J Pediatr Urol. 2021 Jun;17(3):338-345. doi: 10.1016/j.jpurol.2021.02.011. Epub 2021 Feb 17.
Issues and concerns regarding surgery of the sexual-reproductive anatomy during infancy and early childhood are discussed using four actual examples. A case of a 46, XX infant with 21 hydroxylase deficiency congenital adrenal hyperplasia (CAH) with atypical (ambiguous) genitalia is discussed regarding timing and potential harms and benefits of surgery. We present the perspective of balancing the child's rights to bodily autonomy and right to an open future versus parents' decision making authority regarding what they perceive as their child's future best interests. The second case is a newborn with complete androgen insensitivity syndrome and we discuss the harms, benefits and timing of gonadectomy. The third case examines the physical and psychological impact of penile shaft hypospadias, raising the question of whether surgery is justified to prevent what may or may not be considered a permanent disability. The fourth case involves an adult woman with classic CAH, born with a urogenital sinus and clitoromegaly, who never had genital surgery and is now requesting vaginoplasty, but not clitoral reduction. The primary message of this article, as the previous articles in this series, is to encourage patient-family centered care that individualizes treatment guided by shared decision making.
使用四个实际案例讨论了婴儿期和幼儿期性生殖解剖结构手术的问题和关注点。讨论了患有 21 羟化酶缺乏先天性肾上腺皮质增生症(CAH)的 46,XX 婴儿的病例,该婴儿具有非典型(模糊)生殖器,涉及手术的时机以及潜在的危害和益处。我们提出了平衡儿童的身体自主权利和对开放未来的权利与父母对他们认为对孩子未来最佳利益的决策权威的观点。第二个病例是一名患有完全雄激素不敏感综合征的新生儿,我们讨论了性腺切除术的危害、益处和时机。第三个病例研究了阴茎干下裂的身体和心理影响,提出了是否有理由进行手术以预防可能或不可能被认为是永久性残疾的问题。第四个病例涉及一名患有经典 CAH 的成年女性,出生时患有尿生殖窦和阴蒂肥大,从未接受过生殖器手术,现在要求行阴道成形术,但不要求行阴蒂缩小术。本文的主要信息,与本系列中的前几篇文章一样,是鼓励以患者-家庭为中心的护理,根据共享决策指导个体化治疗。