Boston Children's Hospital, 300 Longwood Avenue, Boston, MA, 02115, USA.
Boston Children's Hospital, 300 Longwood Avenue, Boston, MA, 02115, USA.
J Pediatr Urol. 2018 Oct;14(5):416.e1-416.e5. doi: 10.1016/j.jpurol.2018.04.029. Epub 2018 Jun 1.
A central ethical dilemma in management of the patient with a disorder of sex development (DSD) is the potential conflict between respect for the fundamental right of the child for physical and emotional integrity and self-determination, and the right of parents to serve as surrogate decision-makers and act in their child's best interest.
Over the past 2 years we have encountered three complex DSD cases on the spectrum of mixed gonadal dysgenesis to ovotesticular DSD in which gender assignment and therefore optimal surgical management was uncertain. All patients had mosaic karyotypes with Y chromosome, dysgenetic ovary and dysgenetic testis, a urogenital sinus, and prominent phallus. In all three cases a team approach was taken to assess functional potential and risks along either gender pathway and to develop a spectrum of treatment options for parental consideration, including: 1. masculinization with removal of dysgenetic ovary; 2. initial vaginoplasty but with retention of the phallus (±bilateral gonadectomy); 3. initial vaginoplasty with "burial" of corporal bodies (Pippi Salle procedure) (±bilateral gonadectomy); 4. full feminization: vaginoplasty and clitoroplasty (with bilateral gonadectomy); 5. no surgical intervention.
In all three cases, after consideration of risks and benefits of all options, parents selected option 2: gonadectomy to eliminate tumor risk and vaginoplasty, taking advantage of the child's young age to exteriorize urinary and reproductive tracts to avoid incontinence and infection and supporting parental bias toward female gender, but preservation of phallic structures to ensure a male option should the patient later declare a male gender identity. Parents of the three patients were contacted post-operatively (at 7, 17, and 22 months) for follow-up. All (3/3) regarded their child's development and wellbeing positively, and their own decisions regarding gender assignment and surgical plan favorably. All (3/3) regarded the team advisory process as balanced and supportive.
In the setting of exposure of the neonatal brain to testosterone, vaginoplasty and phallic preservation afforded a balance between parental preferences and preservation of anatomic options, allowing potential reconstruction of male or female phenotype as gender identity is ascertained thereby respecting both parent and patient rights. Parents valued a spectrum of options, transparency, and the team decision-making process.
在患有性发育障碍(DSD)的患者的管理中,一个核心的伦理困境是尊重儿童身体和情感完整性以及自我决定的基本权利与父母作为代理人做出决策并为孩子的最佳利益行事的权利之间潜在的冲突。
在过去的 2 年中,我们在混合性腺发育不全到卵睾性 DSD 谱系中遇到了 3 例复杂的 DSD 病例,其中性别分配以及因此最佳手术管理不确定。所有患者均具有嵌合体核型、发育不良的卵巢和发育不良的睾丸、尿生殖窦和突出的阴茎。在所有 3 例病例中,均采用团队方法评估沿任何性别途径的功能潜力和风险,并为父母考虑制定一系列治疗方案,包括:1. 去势化以去除发育不良的卵巢;2. 初始阴道成形术,但保留阴茎(±双侧性腺切除术);3. 初始阴道成形术伴 corpora 体“埋藏”(Pippi Salle 手术)(±双侧性腺切除术);4. 完全女性化:阴道成形术和阴蒂成形术(双侧性腺切除术);5. 无手术干预。
在所有 3 例病例中,在考虑了所有选择的利弊后,父母选择了选项 2:性腺切除术以消除肿瘤风险和阴道成形术,利用孩子的年轻优势将尿生殖管道外化,以避免失禁和感染,并支持父母对女性性别的偏见,但保留阴茎结构,以便患者以后宣布男性性别认同时可以选择男性。术后联系了 3 例患者的父母(7、17 和 22 个月)进行随访。所有(3/3)都对孩子的发育和幸福感持积极态度,对自己的性别分配和手术计划做出了有利的决定。所有(3/3)都认为团队咨询过程是平衡和支持的。
在新生儿大脑暴露于睾酮的情况下,阴道成形术和阴茎保留在父母的偏好和保留解剖学选择之间取得了平衡,从而允许在确定性别认同时重建男性或女性表型,从而既尊重父母的权利又尊重患者的权利。父母重视一系列选择、透明度和团队决策过程。