Kadoya Yoshito, Kenzaka Tsuneaki, Oda Yohei, Matoba Satoaki
Department of Cardiovascular Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, 602-8566, Japan.
Department of Cardiovascular Medicine, Kyotango City Yasaka Hospital, Kyoto, Japan.
BMC Cardiovasc Disord. 2018 Jul 16;18(1):148. doi: 10.1186/s12872-018-0878-1.
In patients with Noonan syndrome (NS), cardiac disorders such as pulmonary valve stenosis (PS) or hypertrophic cardiomyopathy (HCM) are common. While some patients can develop heart failure associated with HCM, the long-term outcome of adult patients with NS is reported to be good. Fatal outcomes of heart failure in patients with NS but without HCM are rare.
We report a 25-year-old Japanese woman diagnosed with NS in adulthood. She exhibited short stature and minor facial dysmorphism and was diagnosed with PS at 1 year of age. After surgical valvuloplasty for PS at 6 years of age, her general condition became stable without specific medical treatment. She discontinued regular medical follow-up for PS. At 21 years of age, she developed acute decompensated heart failure, which was mainly right-sided heart failure due to severe pulmonary regurgitation (PR) and tricuspid regurgitation (TR). There was no evidence of HCM or PS recurrence. On the basis of the history of PS and characteristic physical features including short stature, webbed neck, and hypertelorism, she was clinically diagnosed with NS. At 25 years of age, she developed heart failure of both sides due to PR, TR and late-onset severe mitral stenosis (MS). The etiology of MS was uncertain. Owing to the patient's condition, surgical options were considered to be extremely high risk. She was treated with optimal medical treatment as well as the occasional abdominal cavity drainage for recurrent ascites; however, she died of decompensated heart failure at 27 years of age.
We describe an adult patient with NS without HCM who died of heart failure caused by severe PR, TR and MS. Clinicians should recognize that ongoing or late-onset cardiac disorders can develop in patients with NS, and lead to fatal heart failure. Optimal medical follow-up to monitor cardiac function and early identification of heart failure are important.
在努南综合征(NS)患者中,心脏疾病如肺动脉瓣狭窄(PS)或肥厚型心肌病(HCM)很常见。虽然一些患者可能会发展为与HCM相关的心力衰竭,但据报道成年NS患者的长期预后良好。NS患者但无HCM的心力衰竭致死结局罕见。
我们报告一名成年后被诊断为NS的25岁日本女性。她身材矮小且有轻微面部畸形,1岁时被诊断为PS。6岁时因PS接受手术瓣膜成形术后,她的一般状况稳定,无需特殊治疗。她停止了对PS的定期医学随访。21岁时,她出现急性失代偿性心力衰竭,主要是由于严重的肺动脉反流(PR)和三尖瓣反流(TR)导致的右心衰竭。没有HCM或PS复发的证据。基于PS病史以及包括身材矮小、蹼颈和眼距增宽等特征性体征,她被临床诊断为NS。25岁时,她因PR、TR和迟发性严重二尖瓣狭窄(MS)发展为双侧心力衰竭。MS的病因不明。由于患者的病情,手术选择被认为风险极高。她接受了最佳药物治疗以及偶尔因复发性腹水进行的腹腔引流;然而,她在27岁时死于失代偿性心力衰竭。
我们描述了一名无HCM的成年NS患者,其死于由严重PR、TR和MS引起的心力衰竭。临床医生应认识到NS患者可能会出现持续或迟发性心脏疾病,并导致致命的心力衰竭。监测心脏功能的最佳医学随访以及心力衰竭的早期识别很重要。