lipedema

Lipedema
  • 文章类型: Journal Article
    我们评估了压缩紧身裤与微按摩结合体力活动对患有脂水肿的女性的影响,以前没有治疗,最近没有体重变化。治疗导致所有主观参数的改善,在自发和诱发的疼痛中,在四肢的体积中,在体重没有显著变化的情况下,无论使用时间如何,年龄,多年的疾病,临床阶段,体重指数(BMI)。在未治疗的脂水肿影响的区域,诱发的疼痛没有改善;脚周没有增加。我们发现在下肢多个点评估的皮下脂肪组织(SAT)和皮肤厚度显着减少。建议将微按摩压缩绑腿作为保守治疗的组成部分。提出了一种临床评估诱发疼痛的方法,称为渐进性疼痛检查(PPC),它允许计算称为Ricolfi-Patton评分(RPS)的数值分数,并用于组织的超声评估。该方法简单且可重复,可以在诊断时完成对患者的临床评估,并可以评估各种治疗的效果。甚至只适用于身体的一侧。
    We evaluated the effect of compression leggings with micromassage in association with physical activity on women with lipedema, not previously treated and without recent changes in body weight. The treatment resulted in an improvement in all subjective parameters, in spontaneous and evoked pain, in the volume of the limbs, in the absence of significant changes in body weight, and regardless of the duration of use, age, years of illness, the clinical stage, and body mass index (BMI). Evoked pain did not improve in areas affected by untreated lipedema; foot circumferences did not increase. We found a significant reduction in the thickness of subcutaneous adipose tissue (SAT) and skin evaluated in multiple points of the lower limb. Micromassage compression leggings are proposed as an integral part of conservative treatment. A method is proposed for the clinical evaluation of evoked pain, called the Progressive Pain Check (PPC), which allows for the calculation of a numerical score called the Ricolfi-Patton Score (RPS) and for the ultrasound evaluation of tissues. The method is simple and repeatable and allows for completion of the clinical evaluation of the patient at diagnosis and for an evaluation of the effects of various treatments, even applied to just one side of the body.
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  • 文章类型: Journal Article
    目的:意大利汽车与运动科学学会(SocietàItalianadiScienzeMotorieeSportive,SISMeS)和意大利人口学学会(SocietàItalianadiFlebologia,SIF)提供了关于运动作为非药理学方法在脂水肿中的作用的官方观点。详细来说,这份共识声明SISMeS-SIF旨在全面概述lipedema,聚焦,特别是,关于体育锻炼(PE)在其临床特征管理中的作用。
    结果:脂肪水肿是一种以脂肪积累异常为特征的慢性疾病。常被误诊为肥胖,尽管呈现出不同的病理机制。的确,最近的证据报道了脂肪组织组织学的差异,代谢组学概况,以及与这种情况相关的基因多态性,为复杂的脂水肿病理生理学难题增加新的部分。虽然根据定义,脂水肿是一种对饮食和PE有抵抗力的疾病,后者因其在脂脉管理中的关键作用而出现,为多种福利做出贡献,包括线粒体功能的改善,淋巴引流,减少炎症。各种类型的运动,例如水上运动和力量训练,已被证明可以缓解症状并改善患者的生活质量。然而,缺乏PE处方和脂肪水肿患者长期管理的标准化指南,强调需要在这一领域提出建议和进一步研究,以优化治疗策略。
    OBJECTIVE: This consensus statement from the Italian Society of Motor and Sports Sciences (Società Italiana di Scienze Motorie e Sportive, SISMeS) and the Italian Society of Phlebology (Società Italiana di Flebologia, SIF) provides the official view on the role of exercise as a non-pharmacological approach in lipedema. In detail, this consensus statement SISMeS - SIF aims to provide a comprehensive overview of lipedema, focusing, in particular, on the role played by physical exercise (PE) in the management of its clinical features.
    RESULTS: Lipedema is a chronic disease characterized by abnormal fat accumulation. It is often misdiagnosed as obesity, despite presenting distinct pathological mechanisms. Indeed, recent evidence has reported differences in adipose tissue histology, metabolomic profiles, and gene polymorphisms associated with this condition, adding new pieces to the complex puzzle of lipedema pathophysiology. Although by definition lipedema is a condition resistant to diet and PE, the latter emerges for its key role in the management of lipedema, contributing to multiple benefits, including improvements in mitochondrial function, lymphatic drainage, and reduction of inflammation. Various types of exercise, such as aquatic exercises and strength training, have been shown to alleviate symptoms and improve the quality of life of patients with lipedema. However, standardized guidelines for PE prescription and long-term management of patients with lipedema are lacking, highlighting the need for recommendations and further research in this area in order to optimise therapeutic strategies.
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  • 文章类型: Journal Article
    淋巴水肿和脂肪水肿是慢性衰弱性疾病,最常影响上肢和下肢。虽然它们看起来很相似,它们在重要方面有所不同,本文作者对此进行了回顾和对比。
    Lymphedema and lipedema are chronic debilitating disorders that most commonly affect the upper and lower extremities. Although they can appear similar, they differ in important ways, which the authors of this article review and contrast.
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  • 文章类型: Journal Article
    脂肪水肿和淋巴水肿是物理上相似但不同的疾病,通常被误诊。我们以前报道过,脂肪水肿和淋巴水肿与静脉血栓栓塞(VTE)的风险增加有关。在脂肪水肿和淋巴水肿中观察到的血栓形成的潜在病因尚不清楚。但可能与血小板改变有关.我们的目的是分析血小板转录组,以确定可能提供对血小板活化和血栓形成的见解的生物学途径。在淋巴水肿和脂肪水肿患者中评估血小板转录组,然后与肥胖对照组进行比较。发现与淋巴水肿患者的转录组不同。脂肪水肿的血小板转录组和受影响的生物学途径与体重匹配的比较者惊人地相似,但与体重指数(BMI)较低的超重个体相比却有所不同。在脂肪水肿和淋巴水肿患者的血小板转录组的差异在蛋白质合成和降解所需的生物学途径中发现,以及新陈代谢。与BMI匹配的受试者相比,脂水肿患者的血小板转录组的关键差异涉及代谢和糖胺聚糖加工。血小板转录组的这些固有差异需要进一步研究,并可能增加患者的血栓形成的风险与淋巴水肿。
    Lipedema and lymphedema are physically similar yet distinct diseases that are commonly misdiagnosed. We previously reported that lipedema and lymphedema are associated with increased risk for venous thromboembolism (VTE). The underlying etiology of the prothrombotic profile observed in lipedema and lymphedema is unclear, but may be related to alterations in platelets. Our objective was to analyze the platelet transcriptome to identify biological pathways that may provide insight into platelet activation and thrombosis. The platelet transcriptome was evaluated in patients with lymphedema and lipedema, then compared to control subjects with obesity. Patients with lipedema were found to have a divergent transcriptome from patients with lymphedema. The platelet transcriptome and impacted biological pathways in lipedema were surprisingly similar to weight-matched comparators, yet different when compared to overweight individuals with a lower body mass index (BMI). Differences in the platelet transcriptome for patients with lipedema and lymphedema were found in biological pathways required for protein synthesis and degradation, as well as metabolism. Key differences in the platelet transcriptome for patients with lipedema compared to BMI-matched subjects involved metabolism and glycosaminoglycan processing. These inherent differences in the platelet transcriptome warrant further investigation, and may contribute to the increased risk of thrombosis in patients with lipedema and lymphedema.
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  • 文章类型: Journal Article
    背景:尽管它在整个西方国家的发病率和患病率都在增加,脂水肿仍然是一种非常神秘的疾病,经常被医学界误解或误诊,并且具有难以追踪的内在病理。脂质组织的性质是脂肪细胞肥大和组织更新不良之一。到目前为止,没有确定的途径负责,对脂肪的细胞群知之甚少。方法:从脂肪水肿和健康参与者的受影响区域收集脂肪组织样本。对于单细胞RNA测序分析,使用酶消化将样品解离成单细胞悬浮液,然后包封到含有条形码珠子的纳升大小的液滴中。在每个液滴中,细胞mRNA转化为互补DNA。然后扩增互补DNA分子用于下游分析。结果:单细胞RNA测序分析显示三种不同的脂肪细胞群体在脂肪水肿中起作用。这些群体具有独特的基因特征,可以表征为脂质生成脂肪细胞,疾病催化剂脂肪细胞,和脂肪脂肪细胞。结论:脂质组织样本的单细胞RNA测序突出了不同脂肪细胞亚群的三联体,每个特征都有独特的基因特征和功能作用。这些脂肪细胞亚型之间的相互作用为脂肪水肿的复杂病理生理学提供了有希望的见解。
    Background: Despite its increasing incidence and prevalence throughout Western countries, lipedema continues to be a very enigmatic disease, often misunderstood or misdiagnosed by the medical community and with an intrinsic pathology that is difficult to trace. The nature of lipedemic tissue is one of hypertrophic adipocytes and poor tissue turnover. So far, there are no identified pathways responsible, and little is known about the cell populations of lipedemic fat. Methods: Adipose tissue samples were collected from affected areas of both lipedema and healthy participants. For single-cell RNA sequencing analysis, the samples were dissociated into single-cell suspensions using enzymatic digestion and then encapsulated into nanoliter-sized droplets containing barcoded beads. Within each droplet, cellular mRNA was converted into complementary DNA. Complementary DNA molecules were then amplified for downstream analysis. Results: The single-cell RNA-sequencing analysis revealed three distinct adipocyte populations at play in lipedema. These populations have unique gene signatures which can be characterized as a lipid generating adipocyte, a disease catalyst adipocyte, and a lipedemic adipocyte. Conclusions: The single-cell RNA sequencing of lipedemic tissue samples highlights a triad of distinct adipocyte subpopulations, each characterized by unique gene signatures and functional roles. The interplay between these adipocyte subtypes offers promising insights into the complex pathophysiology of lipedema.
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  • 文章类型: Journal Article
    脂肪瘤症是脂肪组织的良性增生。脂肪瘤(良性脂肪瘤)是脂肪瘤病的最常见成分。它们可能是独一无二的,也可能是多重的,封装或不封装,皮下或有时内脏。在某些情况下,它们形成大面积的非包裹脂肪肥大,纤维化程度不同。尽管没有肥胖,它们仍然可以发展。它们可能是家族性的,也可能是后天获得的。与脂肪营养不良综合征不同,它们与脂肪萎缩区域无关,除了一些罕见的病例,如2型家族性部分脂肪营养不良综合征(FPLD2)。它们的代谢影响是可变的,部分取决于相关的肥胖。它们可能具有功能或美学后果。脂肪瘤病可能是孤立的,是综合症的一部分,或者可能是内脏的。孤立性脂肪瘤病包括多发性对称性脂肪瘤病(Madelung病或Launois-Bensaude综合征),家族性多发性脂肪瘤病,痛苦的皮肤病也被称为肥胖Dolorosa或Ander综合征,间质脂肪瘤病也称为Roch-Leri脂肪瘤病,家族性血管脂肪瘤病,lipedema和hibernomas.综合征性脂肪瘤病包括PIK3CA相关疾病,Cowden/PTEN错构瘤-肿瘤综合征,一些脂肪营养不良综合征,和线粒体疾病,尤其是MERRF,多发性内分泌瘤1型,神经纤维瘤病1型,威尔逊病,Pai或Haberland综合征。最后,内脏脂肪瘤在许多器官和部位都有报道:胰腺,肾上腺,腹部,硬膜外,纵隔,本综述的目的是介绍脂肪瘤病的主要类型及其病理生理成分。当它是已知的。
    Lipomatoses are benign proliferation of adipose tissue. Lipomas (benign fat tumors) are the most common component of lipomatosis. They may be unique or multiple, encapsulated or not, subcutaneous or sometimes visceral. In some cases, they form large areas of non-encapsulated fat hypertrophy, with a variable degree of fibrosis. They can develop despite the absence of obesity. They may be familial or acquired. At difference with lipodystrophy syndromes, they are not associated with lipoatrophy areas, except in some rare cases such as type 2 familial partial lipodystrophy syndromes (FPLD2). Their metabolic impact is variable in part depending on associated obesity. They may have functional or aesthetic consequences. Lipomatosis may be isolated, be part of a syndrome, or may be visceral. Isolated lipomatoses include multiple symmetrical lipomatosis (Madelung disease or Launois-Bensaude syndrome), familial multiple lipomatosis, the painful Dercum\'s disease also called Adiposis Dolorosa or Ander syndrome, mesosomatic lipomatosis also called Roch-Leri lipomatosis, familial angiolipomatosis, lipedema and hibernomas. Syndromic lipomatoses include PIK3CA-related disorders, Cowden/PTEN hamartomas-tumor syndrome, some lipodystrophy syndromes, and mitochondrial diseases, especially MERRF, multiple endocrine neoplasia type 1, neurofibromatosis type 1, Wilson disease, Pai or Haberland syndromes. Finally, visceral lipomatoses have been reported in numerous organs and sites: pancreatic, adrenal, abdominal, epidural, mediastinal, epicardial… The aim of this review is to present the main types of lipomatosis and their physiopathological component, when it is known.
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  • 文章类型: Journal Article
    人工智能(AI)在医疗保健中的作用正在演变,为加强临床决策和患者管理提供有希望的途径。关于脂肪水肿的知识有限通常会导致患者经常被误诊为淋巴水肿或肥胖等疾病,而不是正确识别脂肪水肿。此外,患者往往表现出复杂而广泛的病史,导致协商期间大量的时间消耗。AI可以,因此,改善这些患者的管理。这项研究调查了OpenAI的生成预训练变压器4(GPT-4)的使用,复杂的大型语言模型(LLM),作为脂肪水肿患者咨询的助手。设计了六种模拟方案,以反映在脂水肿诊所中通常遇到的典型患者咨询。GPT-4的任务是进行患者访谈以收集病史,展示其发现,做初步诊断,并建议进一步的诊断和治疗行动。采用了先进的即时工程技术来完善功效,相关性,和GPT-4响应的准确性。一组治疗脂肪斑的专家,用李克特量表,评估了GPT-4在六个关键标准中的响应。得分从1分(最低)到5分(最高),GPT-4的平均得分为4.24,表明在临床环境中具有良好的可靠性和适用性。这项研究是在特定临床场景中应用GPT-4等大型语言模型的初步尝试之一。如脂肪协商。它展示了人工智能在支持临床实践方面的潜力,并强调了人类专业知识在医学领域的持续重要性。尽管技术进步不断。
    The role of artificial intelligence (AI) in healthcare is evolving, offering promising avenues for enhancing clinical decision making and patient management. Limited knowledge about lipedema often leads to patients being frequently misdiagnosed with conditions like lymphedema or obesity rather than correctly identifying lipedema. Furthermore, patients with lipedema often present with intricate and extensive medical histories, resulting in significant time consumption during consultations. AI could, therefore, improve the management of these patients. This research investigates the utilization of OpenAI\'s Generative Pre-Trained Transformer 4 (GPT-4), a sophisticated large language model (LLM), as an assistant in consultations for lipedema patients. Six simulated scenarios were designed to mirror typical patient consultations commonly encountered in a lipedema clinic. GPT-4 was tasked with conducting patient interviews to gather medical histories, presenting its findings, making preliminary diagnoses, and recommending further diagnostic and therapeutic actions. Advanced prompt engineering techniques were employed to refine the efficacy, relevance, and accuracy of GPT-4\'s responses. A panel of experts in lipedema treatment, using a Likert Scale, evaluated GPT-4\'s responses across six key criteria. Scoring ranged from 1 (lowest) to 5 (highest), with GPT-4 achieving an average score of 4.24, indicating good reliability and applicability in a clinical setting. This study is one of the initial forays into applying large language models like GPT-4 in specific clinical scenarios, such as lipedema consultations. It demonstrates the potential of AI in supporting clinical practices and emphasizes the continuing importance of human expertise in the medical field, despite ongoing technological advancements.
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  • 文章类型: Journal Article
    背景:脂水肿是一种以四肢脂肪细胞增多为特征的皮下脂肪组织疾病。维生素D储存在脂肪细胞中,血清水平与BMI呈负相关。由于脂肪细胞在吸脂术中被去除,脂水肿患者可能倾向于进一步大量的维生素D损失,而他们的水平已经下降。因此,我们研究了吸脂术对围手术期血清25-羟维生素D水平的影响.方法:在接受脂水肿吸脂术的患者中,术前和术后采集血样.进行统计分析以关联脂肪抽吸物的体积,患者的BMI和维生素D水平的会议次数。结果:总体而言,对213例患者进行分析。平均吸脂体积为6615.33±3884.25mL,平均BMI为32.18±7.26kg/m2。术前平均维生素D水平为30.1±14.45ng/mL(根据内分泌社会的临界缺乏),术后平均维生素D水平为21.91±9.18ng/mL(缺乏).在我们的患者中,血清维生素D显着降低(p<0.001),平均为7.83ng/mL。在我们的患者中,维生素D的丢失量与BMI或误吸量无关(p>0.05)。有趣的是,无论吸入量或术前水平如何,维生素D动力学均显示稳定下降.结论:许多脂肪水肿患者术前维生素D水平较低。此外,吸脂术显著降低了这些水平,无论吸气量或BMI。然而,维生素D的损失是恒定且可预测的;因此,有风险的患者很容易被识别。总的来说,接受吸脂术的患者容易缺乏维生素D,对这一人群的长期影响目前尚不清楚。
    Background: Lipedema is a subcutaneous adipose tissue disorder characterized by increased pathological adipocytes mainly in the extremities. Vitamin D is stored in adipocytes, and serum levels inversely correlate with BMI. As adipocytes are removed during liposuction, lipedema patients might be prone to further substantial vitamin D loss while their levels are already decreased. Therefore, we examined the effect of liposuction on perioperative serum 25-hydroxyvitamin D levels. Methods: In patients undergoing lipedema liposuction, blood samples were obtained pre- and postoperatively. Statistical analyses were performed to correlate the volume of lipoaspirate, patients\' BMI and number of sessions to vitamin D levels. Results: Overall, 213 patients were analyzed. Mean liposuction volume was 6615.33 ± 3884.25 mL, mean BMI was 32.18 ± 7.26 kg/m2. mean preoperative vitamin D levels were 30.1 ± 14.45 ng/mL (borderline deficient according to the endocrine society) and mean postoperative vitamin D levels were 21.91 ± 9.18 ng/mL (deficient). A significant decrease in serum vitamin D was seen in our patients (p < 0.001) of mean 7.83 ng/mL. The amount of vitamin D loss was not associated with BMI or aspiration volume in our patients (p > 0.05). Interestingly, vitamin D dynamics showed a steady drop regardless of volume aspirated or preoperative levels. Conclusions: Many lipedema patients have low vitamin D levels preoperatively. Liposuction significantly reduced these levels additionally, regardless of aspirated volume or BMI. However, vitamin D loss was constant and predictable; thus, patients at risk are easily identified. Overall, lipedema patients undergoing liposuction are prone to vitamin D deficiency, and the long-term effects in this population are currently unknown.
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  • 文章类型: Journal Article
    Lipedema是一种慢性,特发性,以四肢脂肪组织过多为特征的疼痛疾病。这项研究的目的是表征雌激素受体(ERα和ERβ)的基因表达,G蛋白偶联雌激素受体(GPER),和ER代谢酶:羟基类固醇17-β脱氢酶(HSD17B1,7,B12),细胞色素P450(CYP19A1),激素敏感性脂肪酶(LIPE),酶类固醇硫酸酯酶(STS),和雌激素磺基转移酶(SULT1E1),它们是体重指数(BMI)和年龄匹配的非脂质水肿(健康)和脂质水肿ASC和球体中的标志物。流式细胞术和细胞增殖试验,RT-PCR,和WesternBlot技术用于确定ER和雌激素代谢酶的表达。在2D单层培养中,雌激素增加了间充质标志物的增殖和表达,CD73,在激素耗尽(HD)的健康ASC中与脂肪水肿ASC相比。与相应的健康细胞相比,HD脂肪水肿ASCs和球体中ERβ的表达显着增加。相比之下,在雌激素处理的脂类球体中,ERα和GPER基因表达显着降低。CYP19A1和LIPE基因表达在雌激素处理的健康ASCs和球体中显著增加,分别,而雌激素上调雌激素处理的脂肿分化脂肪细胞和球体中PPAR-2和ERα的表达。这些结果表明,雌激素可能在脂水肿的脂肪组织失调中起作用。
    Lipedema is a chronic, idiopathic, and painful disease characterized by an excess of adipose tissue in the extremities. The goal of this study is to characterize the gene expression of estrogen receptors (ERα and ERβ), G protein-coupled estrogen receptor (GPER), and ER-metabolizing enzymes: hydroxysteroid 17-beta dehydrogenase (HSD17B1, 7, B12), cytochrome P450 (CYP19A1), hormone-sensitive lipase (LIPE), enzyme steroid sulfatase (STS), and estrogen sulfotransferase (SULT1E1), which are markers in Body Mass Index (BMI) and age-matched non-lipedema (healthy) and lipedema ASCs and spheroids. Flow cytometry and cellular proliferation assays, RT-PCR, and Western Blot techniques were used to determine the expression of ERs and estrogen-metabolizing enzymes. In 2D monolayer culture, estrogen increased the proliferation and the expression of the mesenchymal marker, CD73, in hormone-depleted (HD) healthy ASCs compared to lipedema ASCs. The expression of ERβ was significantly increased in HD lipedema ASCs and spheroids compared to corresponding healthy cells. In contrast, ERα and GPER gene expression was significantly decreased in estrogen-treated lipedema spheroids. CYP19A1 and LIPE gene expressions were significantly increased in estrogen-treated healthy ASCs and spheroids, respectively, while estrogen upregulated the expression of PPAR-ϒ2 and ERα in estrogen-treated lipedema-differentiated adipocytes and spheroids. These results indicate that estrogen may play a role in adipose tissue dysregulation in lipedema.
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  • 文章类型: Journal Article
    脂水肿是一种进行性结缔组织疾病,伴有脂肪组织增大,纤维化,流体收集,和真皮增厚。在这里,我们介绍了一例与皮肤灌注不足和溃疡相关的脂肪水肿,其中通过吸脂术使软组织减积改善了患者的症状。一名39岁的女性出现不对称的进行性最初的单侧下肢肿胀,并伴有严重的疼痛,随后出现皮肤溃疡。保守的管理未能改善她的状况。排除其他原因并进行详细的放射学检查后,脂水肿被诊断为相关的皮肤灌注受损。局部伤口护理和压迫疗法的试验未能改善病情。随后通过圆周吸脂术和溃疡清创术以及立即压迫进行的软组织减积显示出症状和皮肤灌注的显着改善。这种情况的独特性质揭示了作为疏松结缔组织疾病的脂水肿。炎症和微血管病变解释了与低灌注和溃疡相关的疼痛非常不典型,部分可能与基质蛋白和钠含量的大量积累有关,导致微血管脆性,伴有频繁的瘀点和血肿以及随后的组织缺血。保守措施如压迫治疗在病程中起着重要作用。手术减积与吸脂术被证明是有效的,在减少软组织负荷和改善四肢疼痛,水肿,周长,和我们病人的皮肤灌注。脂水肿是一种经常误诊的疾病,具有残疾特征。已显示皮肤受累于伴有潜在的灌注不足,需要进一步研究。
    Lipedema is a progressive connective tissue disease with enlargement of adipose tissue, fibrosis, fluid collection, and dermal thickening. Herein, we present a case of lipedema associated with skin hypoperfusion and ulceration in which soft tissue debulking with liposuction improved patients\' symptoms. A 39-year-old female presented with asymmetric progressive initially unilateral lower limb swelling with severe pain with subsequent skin ulceration. Conservative management failed to improve her condition. After excluding other causes and detailed radiologic investigation, lipedema was diagnosed with an associated impaired skin perfusion. Trial of local wound care and compression therapy failed to improve the condition. Subsequent soft tissue debulking with circumferential liposuction and ulcer debridement and immediate compression showed dramatic improvement of the symptoms and skin perfusion. The unique nature of this case sheds light on lipedema as a loose connective tissue disease. Inflammation and microangiopathies explain the associated pain with hypoperfusion and ulceration being quite atypical and in part might be related to the large buildups of matrix proteins and sodium contents leading to fragility in microvessels with frequent petechiae and hematoma and subsequent tissue ischemia. Conservative measures like compression therapy plays a significant role in disease course. Surgical debulking with liposuction was shown to be efficacious in reducing the soft tissue load with improvement in limb pain, edema, circumference, and skin perfusion that was seen in our patient. Lipedema is a frequently misdiagnosed condition with disabling features. Skin involvement in lipedema with potential hypoperfusion was shown and it requires further investigation.
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