Usui Hidehito, Shinkai Masato, Tanaka Satoshi, Morishima Rento, Shirane Kazuki, Kondo Takafumi, Mochizuki Kyoko, Kitagawa Norihiko
Department of Surgery, Kanagawa Children's Medical Center, Yokohama, Japan.
Department of Surgery, Yokohama City University, Yokohama, Japan.
Front Pediatr. 2025 Jun 27;13:1614095. doi: 10.3389/fped.2025.1614095. eCollection 2025.
Superficial lymphatic malformation (SLM), previously known as lymphangioma circumscriptum, is characterized by skin lesions that sometimes require interventional treatment. However, an effective treatment has yet to be established. We proposed an effective sclerotherapy procedure based on the pathophysiology of SLM.
Seven patients with SLM who were treated at our hospital between April 2015 and April 2024 were retrospectively enrolled. To maximize the treatment effects, sclerotherapy with bleomycin targeting the SLM and LM deep beneath the SLM was performed.
Of the seven patients, four were females, and three were males. The SLM sites were mucosal lesions in four cases and skin lesions in three cases. The median age at the first sclerotherapy was 10 (1-18) years. A median of one course (1-3) of sclerotherapy resulted in a marked reduction of SLM lesions on gross evaluation to the satisfaction of the patient. The median observation period was 451 (59-2,901) days. No serious complications occurred, except for transient vomiting in one patient and temporary skin pigmentation in two patients. No patient experienced recurrence requiring retreatment.
Our study suggests that sclerotherapy for the SLM and LM deep beneath the SLM may be an effective treatment for SLM.
浅表淋巴管畸形(SLM),以前称为局限性淋巴管瘤,其特征为皮肤病变,有时需要进行介入治疗。然而,尚未确立有效的治疗方法。我们基于SLM的病理生理学提出了一种有效的硬化治疗方法。
回顾性纳入2015年4月至2024年4月在我院接受治疗的7例SLM患者。为了使治疗效果最大化,对SLM及其下方深部的淋巴管畸形(LM)进行了博来霉素硬化治疗。
7例患者中,4例为女性,3例为男性。SLM部位,4例为黏膜病变,3例为皮肤病变。首次硬化治疗的中位年龄为10(1 - 18)岁。中位1个疗程(1 - 3个疗程)的硬化治疗后,大体评估显示SLM病变明显减轻,患者满意。中位观察期为451(59 - 2901)天。除1例患者出现短暂呕吐和2例患者出现暂时性皮肤色素沉着外,未发生严重并发症。无患者出现需要再次治疗的复发情况。
我们的研究表明,对SLM及其下方深部的LM进行硬化治疗可能是治疗SLM的一种有效方法。