Klippel–Trenaunay综合征患者溃疡不愈合的多重协同治疗

Pub Date : 2023-07-20 DOI:10.3390/reports6030033
Cristina Vocca, Gianmarco Marcianò, Vincenzo Rania, Luca Catarisano, Caterina Palleria, S. Ciranni, G. Torcia, R. Serra, Francesco Monea, G. Spaziano, G. De Sarro, R. Citraro, L. Gallelli
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引用次数: 0

摘要

Klippel–Trenanauy综合征(KTS)是一种罕见的遗传性疾病,由磷脂酰肌醇-4-5-二磷酸3激酶催化亚基(PIK3CA)基因的过度表达决定。临床表现为静脉和毛细血管畸形以及淋巴管畸形。到目前为止,还没有提出明确的治疗方法来改善与皮肤伤口发展相关的临床症状。在这种情况下,我们描述了一名患有KTS的年轻人,他在右下肢出现了严重的皮肤伤口,对普通治疗没有反应,但对氧气臭氧治疗、脉冲磁场(抗磁性治疗)和辛酸钴、油酸、槲皮素和18-β甘草次酸的局部固定结合有反应。这是第一个支持多步骤治疗罕见和严重疾病的病例,我们希望其他研究能够支持我们的数据。
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A Multiple Synergic Treatment for Non-Healing Ulcer Management in a Patient with Klippel–Trenaunay Syndrome
Klippel–Trenanauy syndrome (KTS) is a rare genetic disease determined by overexpression of the phosphatidylinositol-4-5-bisphosphate 3 kinase catalytic subunit (PIK3CA) gene. The clinical presentation is characterized by venous and capillary malformations and lymphatic malformation. To date, no definitive treatment has been suggested in order to improve the clinical symptoms related to the developments of a skin wound. In this case, we describe a young man with KTS that developed a severe skin wound in the lower right limb unresponsive to the common treatment but responsive to a treatment with oxygen-ozone therapy, pulsed magnetic fields (diamagnetic treatment), and topical fixed association of cocum caprylate, oleic acid, quercetin, and 18-β glycyrrhetinic acid. This is the first case that supports a multistep approach to treat a rare and severe disease, and we hope that other studies can support our data.
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