Department of Plastic, Aesthetic, Hand and Reconstructive Micro Surgery, Klinikum Ernst von Bergmann, Potsdam; Department of Plastic, Hand and Reconstructive Surgery, University Hospital Regensburg; Department of Angiology, Klinikum Ernst von Bergmann, Potsdam.
Dtsch Arztebl Int. 2020 Jun 1;117(22-23):396-403. doi: 10.3238/arztebl.2020.0396.
Lipedema is often unrecognized or misdiagnosed; despite an estimated prevalence of 10% in the overall female population, its cause is still unknown. There is increasing awareness of this condition, but its differential diagnosis can still be challenging. In this article, we summarize current hypotheses on its pathogenesis and the recommendations of current guidelines for its diagnosis and treatment.
This review is based on publications about lipedema that were retrieved by a selective search in the MEDLINE, Web of Science, and Cochrane Library databases.
The pathophysiology of lipedema remains unclear. The putative causes that have been proposed include altered adipogenesis, microangiopathy, and disturbed lymphatic microcirculation. No specific biomarker has yet been found, and the diagnosis is currently made on clinical grounds alone. Ancillary tests are used only to rule out competing diagnoses. The state of the evidence on treatment is poor. Treatment generally consists of complex decongestive therapy. In observational studies, liposuction for the permanent reduction of adipose tissue has been found to relieve symptoms to a significant extent, with only rare complications. The statutory healthinsurance carriers in Germany do not yet regularly cover the cost of the procedure; studies of high methodological quality will be needed before this is the case.
The diagnosis of lipedema remains a challenge because of the hetero - geneous presentation of the condition and the current lack of objective measuring instruments to characterize it. This review provides a guide to its diagnosis and treatment in an interdisciplinary setting. Research in this area should focus on the elucidation of the pathophysiology of lipedema and the development of a specific biomarker for it.
脂肪水肿常被误诊或漏诊;尽管估计有 10%的普通女性群体受其影响,但病因仍不明确。尽管人们对这种疾病的认识不断提高,但鉴别诊断仍然具有挑战性。本文总结了目前关于其发病机制的假设以及目前关于其诊断和治疗的指南建议。
本文的综述基于在 MEDLINE、Web of Science 和 Cochrane Library 数据库中进行的选择性检索,检索到关于脂肪水肿的相关文献。
脂肪水肿的病理生理学仍不清楚。提出的可能病因包括脂肪生成改变、微血管病和淋巴微循环紊乱。尚未发现特定的生物标志物,目前仅根据临床标准进行诊断。辅助检查仅用于排除其他竞争诊断。关于治疗的证据状态较差。治疗通常包括复杂的消肿疗法。在观察性研究中,吸脂术永久性减少脂肪组织被发现能显著缓解症状,且并发症罕见。德国的法定健康保险公司目前尚未定期支付该手术的费用;在这种情况下,需要进行高质量的研究。
由于该病的表现存在异质性,且目前缺乏用于对其进行特征描述的客观测量仪器,因此脂肪水肿的诊断仍然具有挑战性。本文为在跨学科环境下对其进行诊断和治疗提供了指南。该领域的研究应集中于阐明脂肪水肿的病理生理学,并开发其特异性生物标志物。