Naito K, Iwata S, Nishimura T, Yagisawa M, Sakurai K
Auris Nasus Larynx. 1985;12(2):111-6. doi: 10.1016/s0385-8146(85)80008-0.
Laryngeal lymphangioma is extremely rare. We have been able to find only seventeen cases reported in world literature. We recently, treated a patient suffering from laryngeal lymphangioma in our department. The female patient, aged 36, complained of hoarseness for several months. Indirect laryngoscopy revealed a growth on her right false vocal cord. Under general anesthesia, tracheostomy and laryngofissure were performed for removal of this neoplasm. The tumor was microscopically diagnosed as lymphangioma. The symptoms disappeared after surgery and there has been no recurrence. The pertinent literature on this rare disease is reviewed.
喉淋巴管瘤极为罕见。我们在世界文献中仅能找到17例相关报道。最近,我们科室治疗了一名患有喉淋巴管瘤的患者。这位36岁的女性患者主诉声音嘶哑数月。间接喉镜检查发现其右侧假声带处有一肿物。在全身麻醉下,行气管切开术和喉裂开术以切除该肿瘤。肿瘤经显微镜检查诊断为淋巴管瘤。术后症状消失,且未出现复发。本文对有关这种罕见疾病的相关文献进行了综述。