Azizkhan Richard G, Rutter Michael J, Cotton Robin T, Lim Lynn H Y, Cohen Aliza P, Mason Jennifer L
Cincinnati Children's Hospital Hemangioma and Vascular Malformation Center, Cincinnati, OH, USA.
J Pediatr Surg. 2006 Jul;41(7):1279-84. doi: 10.1016/j.jpedsurg.2006.03.044.
In light of the paucity of literature on lymphatic malformations of the tongue base, our aim was to present our experience and long-term outcomes of patients with this rare and challenging pathologic entity.
Medical records of 25 patients treated by the 3 senior authors (RGA, MTC, and RTC) between 1974 and 2003 were retrospectively reviewed, and comprehensive clinical data were collected and analyzed.
Twenty-one patients (13 female and 12 male infants) were diagnosed either prenatally or at birth. Of these patients, 18 required early airway stabilization; 17 required tracheotomy. Four patients were diagnosed after 1 year of age and had no airway problems. Follow-up ranged from 2 days (owing to death) to 28 years, with a mean of 10 years. In 21 patients, pathology was extensive, involving contiguous anatomical areas such as the anterior tongue, larynx, pharynx, and floor of mouth. Multiple resections and debulking procedures were performed to restore function and improve cosmesis. Four patients died, all with laryngeal involvement. Of the 14 survivors who had tracheotomies, only 5 are decannulated. Normal oral feeding has been achieved in 14 patients and normal speech, in 8 patients. Cosmesis has improved with time. Orthodontic and dental problems are common, and 9 patients have significant macrognathia.
Although most patients with lymphatic malformations of the tongue base achieve normal oral feeding, airway, speech, and cosmesis issues remain problematic throughout life. Laryngeal involvement signifies extensive disease and is the most significant risk factor for serious complications and death.
鉴于关于舌根淋巴管畸形的文献较少,我们的目的是介绍我们对这种罕见且具有挑战性的病理实体患者的治疗经验和长期预后。
回顾性分析1974年至2003年间由3位资深作者(RGA、MTC和RTC)治疗的25例患者的病历,收集并分析全面的临床数据。
21例患者(13例女性和12例男性婴儿)在产前或出生时被诊断。其中,18例需要早期气道稳定;17例需要气管切开术。4例患者在1岁以后被诊断,且没有气道问题。随访时间从2天(因死亡)到28年不等,平均为10年。21例患者的病变范围广泛,累及相邻的解剖区域,如舌前部、喉、咽和口腔底部。进行了多次切除和减容手术以恢复功能并改善美观。4例患者死亡,均累及喉部。在14例接受气管切开术的幸存者中,只有5例拔管。14例患者实现了正常经口喂养,8例患者实现了正常言语功能。随着时间推移,美观得到改善。正畸和牙齿问题很常见,9例患者有明显的巨颌症。
尽管大多数舌根淋巴管畸形患者实现了正常经口喂养,但气道、言语和美观问题在其一生中仍然存在。喉部受累表明疾病范围广泛,是严重并发症和死亡的最重要危险因素。