Reiter R, Haase S, Brosch S
Univ.-Klinik Ulm, HNO, Sektion Phoniatrie, Frauensteige 12, Ulm.
Laryngorhinootologie. 2010 Jan;89(1):29-33. doi: 10.1055/s-0029-1234044. Epub 2009 Jul 30.
Submucous cleft palate (SMCP) is often diagnosed very late and can cause velopharyngeal insufficiency with open nasal speech and Eustachian tube dysfunction.
A retrospective analysis of 106 patients (100 children, 6 adults) who had been surgically treated for SMCP was made. Age of diagnosis, physician who initially diagnosed the SMCP, typical symptoms for cleft palate, clinical examination of the palate, therapy options and accompanying diseases were evaluated.
SMCP was diagnosed in 79 cases by a specialist for Phoniatrics/ENT surgery of the University and in 21 cases by a physician, who does not work at hospital at the age of 4.9 years. Main symptoms were Eustachian tube dysfunctions (61.3%) and hypernasal speech (48.1%). Typical findings of the palate were: reduced contraction (69.8%), lack of posterior nasal spine (55.7%) and bifid uvula (51.9%). In 18 patients a dysmorphic syndrome was observed and in 83% a conductive hearing loss which resolved after palatoplasty (often in combination with adenotomy and insertion of ventilation tubes). Following surgery 18 patients required speech therapy and of these 6 needed velopharyngoplasty due to continuing open nasal speech.
SMCP is often diagnosed very late, though symptoms of velopharyngeal insufficiency such as open nasal speech, Eustachian tube dysfunction and reduced contraction of the palate with bifid uvula are present. It is also often found in children with craniofacial dysmorphic syndromes. We therefore recommend that all patients with such findings are examined by an appropriate specialist such as Phoniatrics, ENT-Surgeon and Oral-Maxillofacial Surgeon so that early diagnosis and palatoplasty can be performed.
腭黏膜下裂(SMCP)常被诊断得很晚,可导致腭咽闭合不全,出现开放性鼻音和咽鼓管功能障碍。
对106例接受SMCP手术治疗的患者(100例儿童,6例成人)进行回顾性分析。评估诊断年龄、最初诊断SMCP的医生、腭裂的典型症状、腭部的临床检查、治疗方案及伴发疾病。
79例SMCP由大学的语音治疗/耳鼻喉外科专家诊断,21例由非本院医生在4.9岁时诊断。主要症状为咽鼓管功能障碍(61.3%)和开放性鼻音(48.1%)。腭部的典型表现为:收缩减弱(69.8%)、后鼻棘缺失(55.7%)和悬雍垂裂(51.9%)。18例患者观察到畸形综合征,83%患者存在传导性听力损失,腭裂修复术后(常联合腺样体切除术和置放通气管)听力损失得以解决。术后18例患者需要言语治疗,其中6例因持续性开放性鼻音需要进行腭咽成形术。
尽管存在腭咽闭合不全的症状,如开放性鼻音、咽鼓管功能障碍以及腭部收缩减弱伴悬雍垂裂,但SMCP常被诊断得很晚。它也常见于患有颅面畸形综合征的儿童。因此,我们建议所有有此类表现的患者由合适的专科医生,如语音治疗师、耳鼻喉外科医生和口腔颌面外科医生进行检查,以便能早期诊断并实施腭裂修复术。