山东大学学报 (医学版) ›› 2022, Vol. 60 ›› Issue (8): 72-78.doi: 10.6040/j.issn.1671-7554.0.2022.0535
王文静1,刘博策1,毕见海2,霍然1,2
WANG Wenjing1, LIU Boce1, BI Jianhai2, HUO Ran1,2
摘要: 目的 回顾性分析超声引导下平阳霉素联合聚桂醇经皮硬化治疗囊性淋巴管畸形(cLM)的疗效和安全性。 方法 共纳入cLM患者94例,年龄0.5~43岁,儿童患者86例,发病时间在2岁之前75例,巨囊型32例、微囊型31例、混合型31例。 结果 治疗后随访时间3.7~39.2个月,平均治疗次数2.8次,病灶体积减小的有效率为78.7%,症状缓解的有效率为82.1%,患者及家属的满意率为85.1%,14例患者出现不良反应,未出现肺纤维化、过敏等严重不良反应,7例复发患者再次给予治疗,效果好。 结论 超声引导下平阳霉素联合聚桂醇经皮硬化治疗cLM是一种安全有效的方式,值得临床推广。
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[1] 血管瘤和脉管畸形的诊断及治疗指南(2019版)[J].组织工程与重建外科杂志, 2019, 15(5): 277-317. [2] Kulungowski AM, Patel M. Lymphatic malformations [J]. Semin Pediatr Surg, 2020, 29(5): 150971. [3] Mäkinen T, Boon LM, Vikkula M, et al. Lymphatic malformations: genetics, mechanisms and therapeutic strategies [J]. Circ Res, 2021, 129(1): 136-154. [4] Perkins JA, Manning SC, Tempero RM, et al. Lymphatic malformations: current cell ularand clinica linvestigations [J]. Otolaryngol Head Neck Surg, 2010, 142(6): 789-794. [5] McCuaig CC. Update on classification and diagnosis of vascular malformations. [J]. Curr Opin Pediatr, 2017, 29(4): 448-454. [6] Janardhan HP, Saheera S, Jung R, et al. Vascular and lymphatic malformations: perspectives from human and vertebrate studies [J]. Circ Res, 2021, 129(1): 131-135. [7] De Leacy R, Bageac DV, Manna S, et al. A radiologic grading system for assessing the radiographic outcome of treatment in lymphatic and lymphatic-venous malformations of the head and neck [J]. AJNR Am J Neuroradiol, 2021, 42(10): 1859-1864. [8] Berenstein A, Bazil MJ, Sorscher M, et al. Percutaneous sclerotherapy of microcystic lymphatic malformations: the use of an innovative gravity-dependent technique [J]. J Neurointerv Surg, 2022, 28: 018526. doi: 10.1136/neurintsurg-2021-018526. [9] Elluru RG, Balakrishnan K, Padua HM. Lymphatic malformations: diagnosis andmanagement [J]. Semin Pediatr Surg,2014,23(4): 178-185. [10] Cursiefen C, Chen L, Dana MR, et al. Corneal lymphangiogenesis: evidence, mechanism, and implications for corneal transplant immunology [J]. Cornea, 2003, 22(3): 273-281. [11] Liersch R, Detmar M. Lymphangiogenesis in development and disease [J]. Thromb Haemost, 2007, 98(2): 304-310. [12] Bekisz S, Baudin L, Buntinx F, et al. In vitro, in vivo, and in silico models of lymphangiogenesis in solid malignancies [J]. Cancers(Basel), 2022,14(6):1525. [13] Oliver G. Lymphatic vasculature development [J]. Nat Rev Immunol, 2004,4(1): 35-45. [14] Luks VL, Kamitaki N, Vivero MP, et al. Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA [J]. J Pediatr,2015,166:1048-1054. doi: 10.1016/j.jpeds.2014.12.069. [15] Zenner K, Jensen DM, Dmyterko V, et al. Somatic activating BRAF variants. cause isolated lymphatic malformations [J]. HGG Adv,2022,3(2):100101. [16] Martinez-Corral I, Zhang Y, Petkova M, et al. Blockade of VEGF-C signaling inhibits lymphatic malformations driven by oncogenic PIK3CA mutation [J]. Nat Commun,2020,11(1):2869. [17] Kato M, Watanabe S, Iida T, et al. Flow pattern classification in lymphatic malformations by indocyanine green lymphography [J]. Plast Reconstr Surg, 2019,143(3):558e-564e. [18] Bhatnagar A, Neyaz Z, Singh B, et al. Bleomycin sclerotherapy in massive macrocystic lymphatic malformation: minimal complications with maximum results [J]. J Cutan Aesthet Surg, 2020,13(4):319-325. [19] 谢义民,陈强,王玲,等. 聚桂醇瘤腔内注射治疗小儿囊性淋巴管瘤[J].中华小儿外科杂志,2017,38(9):704-707. XIE Yimin, CHEN Qiang, WANG Ling, et al. Intratumoral injection of lauromacrogol for children with cyctic lymphangioma [J]. Chinese Journal of Pediatric Surgery,2017,38(9):704-707. [20] Fuentes S, Delgado D, Marti E, et al. Treatment of lymphatic malformations with OK-432 sclerosis: our experience [J]. Cir Pediatr,2010,23(2):88-91. [21] Horbach SE, Lokhorst MM, Saeed P, et al. Sclerotherapy for low-flow vascular malformations of the head and neck: a systematic review of sclerosing agents [J]. J Plast Reconstr Aesthetic Surg, 2016, 69:295-304. doi: 10.1016/j.bjps.2015.10.045. [22] Fernandes S, Yeung P, Heran M, et al. Sclerosing agents in the management of lymphatic malformations in children: a systematic review [J]. J Pediatr Surg, 2022, 57(5):888-896. [23] Al-Faky YH, Alkatan HM. Histopathological changes of lymphatic malformation after bleomycin injection [J]. Arq Bras Oftalmol, 2022, 21:s0004. doi: 10.5935/0004-2749.20230048. [24] Cho AL, Kiang SC, Lodenkamp J, et al. Fatal lung toxicity after intralesionalbleomycin sclerotherapy of a vascular malformation [J]. Cardiovasc Intervent Radiol,2020,43(4):648-651. [25] Blaise S, Charavin-Cocuzza M, Riom H, et al. Treatment of low-flow vascular malformations by ultrasound-guided sclerotherapy with polidocanol foam: 24 cases and literature review [J]. Eur J Vasc Endovasc Surg, 2011,41(3):412-417. |
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