Al-Salem Ahmed H
Department of Surgery, Division of Pediatric Surgery, Qatif Central Hospital, Qatif, Kingdom of Saudi Arabia.
Saudi Med J. 2004 Apr;25(4):466-9.
Lymphangiomas are rare congenital malformations, commonly seen in the head and neck. This is a review of our experience in the management of 22 children with lymphangiomas.
The medical records of children with lymphangioma admitted to Qatif Central Hospital, Qatif, Kingdom of Saudi Arabia over a period of 10 years from August 1989 to July 2000 were retrospectively reviewed for age at diagnosis, gender, mode of presentation, site of lymphangioma, method of treatment and outcome.
We treated 22 children (12 females and 10 males) with lymphangioma. Their ages ranged from birth to 12 years, but majority (73%) were 4 years of age or younger. In 10 (45.5%), the lymphangioma involved the neck, 5 of them presented with sudden neck swelling as a result of hemorrhage into a lymphangioma, which caused diagnostic confusion. One patient had extensive lymphangioma involving the floor of the mouth, tongue, and left parotid gland. The remaining 11 patients had lymphangioma involving the parotid gland in 2, floor of the mouth in 3, and one each in the abdominal wall, above the right knee, mediastinum, breast, scrotum, and mesentery. All were treated surgically except 3 who were treated with intralesional bleomycin and showed complete disappearance of their lesions. There was recurrence in the child with mediastinal lymphangioma and a small recurrence in the child with bilateral lesions in the floor of the mouth.
Lymphangiomas are relatively rare, involving mainly the head and neck, but they can be rarely seen at other sites. An important observation is the sudden appearance of cervical lymphangioma as a result of hemorrhage, which should be kept in mind. Our experience in the treatment of lymphangiomas using bleomycin is limited to draw any conclusions. We therefore considered surgery as treatment of choice for lymphangiomas. However, sclerotherapy can be used when there is a risk of damaging surrounding structures, and also to obviate the poor cosmetic results.
淋巴管瘤是罕见的先天性畸形,常见于头颈部。本文回顾了我们治疗22例儿童淋巴管瘤的经验。
回顾性分析1989年8月至2000年7月期间沙特阿拉伯卡提夫市卡提夫中心医院收治的淋巴管瘤患儿的病历,记录诊断时的年龄、性别、临床表现方式、淋巴管瘤部位、治疗方法及预后。
我们共治疗22例淋巴管瘤患儿(12例女性,10例男性)。年龄从出生至12岁,但大多数(73%)为4岁及以下。10例(45.5%)淋巴管瘤累及颈部,其中5例因淋巴管瘤内出血导致颈部突然肿胀,造成诊断困难。1例患者的广泛性淋巴管瘤累及口底、舌及左腮腺。其余11例患者中,2例淋巴管瘤累及腮腺,3例累及口底,腹壁、右膝上方、纵隔、乳腺、阴囊及肠系膜各1例。除3例采用瘤内注射博来霉素治疗且病变完全消失外,其余均接受手术治疗。纵隔淋巴管瘤患儿出现复发,口底双侧病变患儿有小的复发。
淋巴管瘤相对罕见,主要累及头颈部,但也可见于其他少见部位。重要的是要注意到颈部淋巴管瘤可因出血而突然出现。我们使用博来霉素治疗淋巴管瘤的经验有限,无法得出任何结论。因此,我们认为手术是治疗淋巴管瘤的首选方法。然而,当存在损伤周围结构的风险或为避免不良美容效果时,可采用硬化治疗。