Individualized treatment of congenital vascular malformations of the tongue.

IF 2.1 4区 医学 Q3 HEMATOLOGY
Moritz Guntau, Beatrix Cucuruz, Richard Brill, Oleksandr Bidakov, Susane von der Heydt, Andreas Deistung, Walter A Wohlgemuth
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Abstract

Background/objective: Oral malformations of the tongue are exceedingly rare. The aim of this study was to evaluate the effectiveness of individualized treatment for patients with vascular malformations of the tongue.

Methods: This retrospective study is based on a consecutive local registry at a tertiary care Interdisciplinary Center for Vascular Anomalies. Patients with vascular malformations of the tongue were included. Indications for therapy of the vascular malformation were macroglossia with the impossibility to close the mouth, bleeding, recurrent infection and dysphagia. Size regression of the malformation (volume measurement) and symptom improvement were investigated.

Results: Out of 971 consecutive patients with vascular malformations, 16 patients suffered from a vascular malformation of the tongue. Twelve patients had slow-flow malformations and 4 fast-flow malformations. Indications for interventions were bleeding (4/16, 25%), macroglossia (6/16, 37.5%), and recurrent infections (4/16, 25%). For two patients (2/16, 12.5%), there was no indication for intervention due to absence of symptoms. Four patients received sclerotherapy, 7 patients Bleomycin-electrosclerotherapy (BEST) and 3 patients embolization. Median follow-up was 16 months (IQR 7-35.5). In all patients, symptoms had decreased after two interventions at a median (IQR 1-3.75). Volume reduction of the malformation of the tongue was 13.3% (from median 27.9 cm3 to median 24.2 cm3, p = 0.0039), and even more pronounced when considering only patients with BEST (from 86 cm3 to 59.1 cm3, p = 0.001).

Conclusion: Symptoms of vascular malformations of the tongue are improved after a median of two interventions with significantly increased volume reduction after Bleomycin-electrosclerotherapy.

先天性舌血管畸形个体化治疗。
背景/目的:口腔舌畸形极为罕见。本研究的目的是评估个体化治疗舌血管畸形的有效性。方法:这项回顾性研究是基于一个三级保健跨学科血管异常中心的连续本地登记。包括舌部血管畸形患者。血管畸形的适应症为巨舌不能闭口、出血、反复感染、吞咽困难。观察畸形大小回归(体积测量)及症状改善情况。结果:971例血管畸形患者中,16例发生舌部血管畸形。慢流畸形12例,快流畸形4例。干预的指征为出血(4/16,25%)、大舌裂(6/16,37.5%)和复发性感染(4/16,25%)。2例(2/16,12.5%)患者无症状,无干预指征。硬化治疗4例,博莱霉素电硬化治疗(BEST) 7例,栓塞治疗3例。中位随访16个月(IQR 7-35.5)。在所有患者中,两次干预后症状均有所减轻(IQR 1-3.75)。舌部畸形体积缩小13.3%(从中位27.9 cm3到中位24.2 cm3, p = 0.0039),仅考虑BEST患者时更明显(从86 cm3到59.1 cm3, p = 0.001)。结论:博莱霉素电硬化治疗后,舌头血管畸形的症状在两次干预的中位数后得到改善,体积缩小明显增加。
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来源期刊
CiteScore
4.30
自引率
33.30%
发文量
170
期刊介绍: Clinical Hemorheology and Microcirculation, a peer-reviewed international scientific journal, serves as an aid to understanding the flow properties of blood and the relationship to normal and abnormal physiology. The rapidly expanding science of hemorheology concerns blood, its components and the blood vessels with which blood interacts. It includes perihemorheology, i.e., the rheology of fluid and structures in the perivascular and interstitial spaces as well as the lymphatic system. The clinical aspects include pathogenesis, symptomatology and diagnostic methods, and the fields of prophylaxis and therapy in all branches of medicine and surgery, pharmacology and drug research. The endeavour of the Editors-in-Chief and publishers of Clinical Hemorheology and Microcirculation is to bring together contributions from those working in various fields related to blood flow all over the world. The editors of Clinical Hemorheology and Microcirculation are from those countries in Europe, Asia, Australia and America where appreciable work in clinical hemorheology and microcirculation is being carried out. Each editor takes responsibility to decide on the acceptance of a manuscript. He is required to have the manuscript appraised by two referees and may be one of them himself. The executive editorial office, to which the manuscripts have been submitted, is responsible for rapid handling of the reviewing process. Clinical Hemorheology and Microcirculation accepts original papers, brief communications, mini-reports and letters to the Editors-in-Chief. Review articles, providing general views and new insights into related subjects, are regularly invited by the Editors-in-Chief. Proceedings of international and national conferences on clinical hemorheology (in original form or as abstracts) complete the range of editorial features.
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