Doença vascular inflamatória não necrosante rara que afeta as artérias e veias de pequeno e médio calibre das extremidades superiores e inferiores, caracterizada por endarterite e vaso-oclusão devido ao desenvolvimento de trombo oclusivo. O desenvolvimento e progressão da doença estão consistentemente associados à exposição ao tabaco.
Introdução
O que você precisa saber de cara
Doença vascular inflamatória não necrosante rara que afeta as artérias e veias de pequeno e médio calibre das extremidades superiores e inferiores, caracterizada por endarterite e vaso-oclusão devido ao desenvolvimento de trombo oclusivo. O desenvolvimento e progressão da doença estão consistentemente associados à exposição ao tabaco.
Escala de raridade
<1/50kMuito rara
1/20kRara
1/10kPouco freq.
1/5kIncomum
1/2k
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Sinais e sintomas
O que aparece no corpo e com que frequência cada sintoma acontece
Partes do corpo afetadas
+ 14 sintomas em outras categorias
Características mais comuns
Os sintomas variam de pessoa para pessoa. Abaixo estão as 20 características clínicas mais associadas, ordenadas por frequência.
Linha do tempo da pesquisa
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Genética e causas
O que está alterado no DNA e como passa nas famílias
Nenhum gene associado encontrado
Os dados genéticos desta condição ainda estão sendo catalogados.
Diagnóstico
Os sinais que médicos procuram e os exames que confirmam
Tratamento e manejo
Remédios, cuidados de apoio e o que precisa acompanhar
Onde tratar no SUS
Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)
🇧🇷 Atendimento SUS — Doença de Buerger
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Outros ensaios clínicos
19 ensaios clínicos encontrados, 3 ativos.
Publicações mais relevantes
The Diagnostic Pitfall of Ankle-Brachial Index in Buerger Disease: Can We Trust Pressure Measurements in the Presence of Corkscrew Collaterals?
To evaluate the diagnostic performance of the ankle-brachial index (ABI) in patients with Buerger disease and to assess the impact of collateral circulation on ankle pressure measurements in the presence of angiographically confirmed infrapopliteal arterial occlusions. This retrospective study included 66 lower limbs from 45 male patients (mean age, 45.4 years [SD ± 9.7]) diagnosed with Buerger disease. All patients underwent digital subtraction angiography (DSA) and ABI measurement prior to endovascular intervention. Limbs were categorized according to the angiographic patency of the anterior and posterior tibial arteries. ABI diagnostic performance was evaluated using DSA as the reference standard, with emphasis on the prevalence of normal ABI values (≥0.90) in limbs with complete tibial artery occlusion. Angiography demonstrated complete occlusion of both tibial arteries in 50 of 66 limbs (75.7%). Despite severe infrapopliteal disease, 21 of these 50 limbs (42.0%) exhibited normal ABI values, indicating a high false-negative rate. The mean ABI in limbs with complete tibial occlusion was 0.82 (SD ± 0.20). Doppler-derived ankle pressure measurements were obtainable in 94%-98% of occluded tibial arteries due to extensive collateral circulation. ABI values did not differ significantly between limbs with isolated tibial occlusion and those with combined popliteal and tibial artery involvement (P > .05). ABI frequently underestimates disease severity in Buerger disease because collateral networks preserve ankle pressures despite critical infrapopliteal occlusions. ABI should not be used as a standalone screening tool, and adjunct physiologic testing or imaging is required for accurate vascular assessment.
A systematic review and meta-analysis of early and long-term outcomes after endovascular interventions in patients with thromboangiitis obliterans and critical limb ischemia with GRADE assessment.
Thromboangiitis obliterans (TAO) is a rare inflammatory occlusive vascular disorder that affects small and medium-sized vessels and often progresses to critical limb ischemia (CLI). Although various treatments have been used in advanced stages, endovascular interventions have increasingly gained attention as a limb-saving therapy. Due to limited and varied evidence in published studies, this systematic review and meta-analysis evaluates the early and long-term outcomes of endovascular treatments in patients with TAO-related CLI. This systematic review and meta-analysis was conducted according to PRISMA guidelines and registered on PROSPERO (CRD420251089226). PubMed, Scopus, WOS, Embase, and Google Scholar databases were searched with relevant keywords up to July 2025. A total of 27 studies involving 1,217 patients were included. Pooled outcomes were estimated using a generalized linear mixed model (GLMM). Heterogeneity was assessed using the I² statistic, and potential publication bias was examined via funnel plots and Egger’s test. The pooled technical success rate for endovascular procedures was 89%, with limb salvage rates of 94% at 6 months and 97% at 12 months. Primary patency was 56% at 6 months, 73% at 12 months, and 61% at 36 months; these findings highlight temporal variability, and cross-time comparisons should be interpreted with caution. Secondary patency was initially higher but also decreased over long-term follow-up. Restenosis rates were 15% early and 34% late. Major and minor amputation rates were 10% and 13%, respectively. No in-hospital mortality was reported. Endovascular therapy represents a safe and effective option for treating TAO-related CLI, especially in patients who are not candidates for surgery. While early results are promising, the loss of patency and rising restenosis over time highlight the importance of careful follow-up and proper patient selection. Our findings support a personalized, multidisciplinary approach to managing TAO and emphasize the vital role of smoking cessation in improving clinical outcomes. [Image: see text] The online version contains supplementary material available at 10.1186/s12893-026-03563-2.
Seltoplasmid promotes ulcer healing versus placebo for treating patients with chronic limb-threatening ischemia: HOPE CLTI-2 trial.
Intramuscular injection of donaperminogene seltoplasmid (recombinant human hepatocyte growth factor plasmids) represents a gene therapy that treats patients with chronic limb-threatening ischemia (CLTI). The HOPE CLTI-2 trial was a phase 3, multicenter, double-blind, placebo-controlled study aimed to evaluate the efficacy and safety of seltoplasmid in patients with Rutherford class 5 CLTI. This study did not require participants to be ineligible for revascularization, allowing enrollment of patients with CLTI caused by either atherosclerosis (ASO) or Buerger disease (or thromboangiitis obliterans [TAO]). The primary endpoint was the complete ulcer healing rate at 6 months. A total of 242 participants (53.3% ASO versus 46.7% TAO) were enrolled, with 161 receiving seltoplasmid and 81 receiving placebo. Complete ulcer healing was achieved in 70 patients in the seltoplasmid group compared to 15 patients in the placebo group, resulting in an adjusted healing rate difference of 26.1% (95% confidence interval [CI]: 15.1%-37.0%; p < 0.001). The hazard ratio for healing was 2.31 (95% CI: 1.32-4.05; p = 0.004). The benefits of seltoplasmid on ulcer healing persisted in both TAO and ASO subgroups. Serious adverse events were rare. Our study demonstrated that seltoplasmid significantly improved ulcer healing rates in patients with Rutherford class 5 CLTI compared to placebo.
Treatment Options for Buerger Disease: A Systematic Review and Meta-Analysis of Outcomes.
Uncertainties exist regarding the optimal management strategy for patients with thromboangiitis obliterans (TAOs). The aim of this study was to investigate the safety and effectiveness of common interventions used for treating patients with TAO. Endovascular treatment, revascularization, sympathectomy, stem cell therapy (SCT), and nonsurgical interventions were selected for inclusion in the study. Changes in mean visual analogue scale score and ankle brachial index (ABI) values were evaluated. In addition, the rate of ulcer healing, postintervention amputation, and overall complication rates were compared across interventions. A total of 1262 TAO patients (1159 males, 84 females), with a mean age of 38.4 ± 7.8 ys, were included in this systematic review. With an amputation rate of 16.6%, the endovascular treatment group showed statistically significant improvements in mean ABI and visual analogue scale scores (P < 0.05). There was a greater increase in ABI postoperatively with endovascular treatment compared to SCT (P < 0.05), and also a greater increase in ABI postoperatively with revascularization compared to SCT (P < 0.05). Meta-regression showed that both endovascular treatment and open surgical revascularization were superior to stem cell treatment for postoperative mean ABI improvement (P < 0.05). Interestingly, the rate of postoperative amputation was lower in the SCT group compared with the other two interventions. Our results indicated that all three interventions may be a reasonable therapeutic option for TAO. Endovascular intervention and open revascularization demonstrated superior outcomes.
ANCA-Negative Pauci-Immune Crescentic Glomerulonephritis and Buerger Disease.
Publicações recentes
The Diagnostic Pitfall of Ankle-Brachial Index in Buerger Disease: Can We Trust Pressure Measurements in the Presence of Corkscrew Collaterals?
A systematic review and meta-analysis of early and long-term outcomes after endovascular interventions in patients with thromboangiitis obliterans and critical limb ischemia with GRADE assessment.
Seltoplasmid promotes ulcer healing versus placebo for treating patients with chronic limb-threatening ischemia: HOPE CLTI-2 trial.
ANCA-Negative Pauci-Immune Crescentic Glomerulonephritis and Buerger Disease.
Treatment Options for Buerger Disease: A Systematic Review and Meta-Analysis of Outcomes.
📚 EuropePMC111 artigos no totalmostrando 51
The Diagnostic Pitfall of Ankle-Brachial Index in Buerger Disease: Can We Trust Pressure Measurements in the Presence of Corkscrew Collaterals?
Journal of vascular and interventional radiology : JVIRA systematic review and meta-analysis of early and long-term outcomes after endovascular interventions in patients with thromboangiitis obliterans and critical limb ischemia with GRADE assessment.
BMC surgerySeltoplasmid promotes ulcer healing versus placebo for treating patients with chronic limb-threatening ischemia: HOPE CLTI-2 trial.
Molecular therapy : the journal of the American Society of Gene TherapyANCA-Negative Pauci-Immune Crescentic Glomerulonephritis and Buerger Disease.
Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseasesTreatment Options for Buerger Disease: A Systematic Review and Meta-Analysis of Outcomes.
The Journal of surgical researchUltrasonographic Study of the Corkscrew Arterial Image in Buerger Disease Patients.
Annals of vascular diseasesThromboangiitis obliterans (Buerger disease).
Vascular medicine (London, England)Spontaneous Intercostal Artery Bleeding in a Patient With Buerger's Disease: A Case Report.
CureusLow-intensity pulsed ultrasound improves symptoms in patients with Buerger disease: a double-blinded, randomized, and placebo-controlled study.
Scientific reportsVasoactive and Antifibrotic Properties of Cannabinoids and Applications to Vasospastic/Vaso-Occlusive Disorders: A Systematic Review.
Annals of plastic surgeryLow-intensity pulsed ultrasound for 'no-option' chronic/critical limb-threatening ischaemia in a patient with Buerger disease: a case report.
European heart journal. Case reportsTrue leukonychia as the presenting sign of early thromboangiitis obliterans.
JAAD case reportsThe effect of different taping techniques on transtibial amputation walking parameters: A case report.
Prosthetics and orthotics internationalOff-the-shelf percutaneous deep vein arterialization for no-option chronic limb-threatening ischemia related to Buerger disease.
Journal of vascular surgery cases and innovative techniquesThe Effect of Smoking Cessation on the Technical Success of Endovascular Treatment for Thromboangiitis Obliterans.
Journal of vascular and interventional radiology : JVIRDo Patients With Arterial Occlusive Disease of Different Etiologies Benefit Equally From Cilostazol?
Texas Heart Institute journalA systematic review and meta-analysis of early and late outcomes after endovascular angioplasty among patients with thromboangiitis obliterans and chronic limb ischemia.
Journal of vascular surgeryBuerger Disease: Pathological Changes in Elderly Patients.
Annals of vascular diseasesNails Involvement in Winiwarter-Buerger Disease.
Skin appendage disordersEstimate and Temporal Trends of Buerger Disease Hospitalizations in the United States.
The American journal of cardiologyThe historical differential diagnosis of the disease that afflicted Aleijadinho, the famous 18th century Brazilian sculptor.
Arquivos de neuro-psiquiatriaRecent Updates and Advances in Winiwarter-Buerger Disease (Thromboangiitis Obliterans): Biomolecular Mechanisms, Diagnostics and Clinical Consequences.
Diagnostics (Basel, Switzerland)Pearls & Oy-sters: Primary Cerebral Buerger Disease: A Rare Differential Diagnosis of Stroke in Young Adults.
NeurologyPathological and immunological differences of arterial thrombi and wall caused by three different periodontal bacterial injections in rat models and proposals on the pathogeneses of vascular diseases.
Clinical and experimental dental researchLeft Carotid Artery Thrombosis Due to Thromboangiitis Obliterans.
The American journal of forensic medicine and pathologyEndovascular Treatment of Critical Limb Ischemia in Buerger Disease (Thromboangiitis Obliterans) With Midterm Follow-Up: A Viable Option When Bypass Surgery Is Not Feasible.
AJR. American journal of roentgenologyThe Imbalance among Oxidative Biomarkers and Antioxidant Defense Systems in Thromboangiitis Obliterans (Winiwarter-Buerger Disease).
Journal of clinical medicineLong-Term Clinical Outcomes of Autologous Bone Marrow Mononuclear Cell Implantation in Patients With Severe Thromboangiitis Obliterans.
Circulation journal : official journal of the Japanese Circulation SocietyD-dimer levels in patients with thromboangiitis obliterans.
The National medical journal of IndiaSuccessful Fat Grafting in a Patient With Thromboangiitis Obliterans.
Advances in skin & wound careMajor lower extremity amputation: a contemporary analysis from an academic tertiary referral centre in a developing community.
BMC surgeryMedical adjunctive therapy for patients with chronic limb-threatening ischemia: a systematic review.
The Journal of cardiovascular surgeryCase report of two pregnancies and deliveries by a woman with Buerger disease.
The journal of obstetrics and gynaecology researchPerformance of noninvasive laser Doppler flowmetry and laser speckle contrast imaging methods in diagnosis of Buerger disease: A case report.
MedicineThree cases of dorsal metatarsal artery bypass in patients with Buerger disease.
Journal of vascular surgery cases and innovative techniques[Digital ischemia revealing multiple myeloma].
Journal de medecine vasculaireImmediate and late outcomes of endovascular therapy for lower extremity arteries in Buerger disease.
Journal of vascular surgeryFour-extremity salvage with long vein grafts in buerger disease.
Archives of plastic surgeryEndothelial dysfunction in patients with Buerger disease.
Vascular health and risk managementProgressive fingertip necrosis after nail avulsion injury in a patient with ulnar artery hypoplasia: A case report.
MedicineAn Experimental Model of Peripheral Vascular Disease Involving the Intravenous Injection of Oral Bacteria.
Annals of vascular diseasesEfficacy of bosentan in patients with refractory thromboangiitis obliterans (Buerger disease): A case series and review of the literature.
MedicineVascular Function and Intima-media Thickness of a Leg Artery in Peripheral Artery Disease: A Comparison of Buerger Disease and Atherosclerotic Peripheral Artery Disease.
Journal of atherosclerosis and thrombosisInvestigation of the Etiology of Anemia in Thromboangiitis Obliterans.
The International journal of angiology : official publication of the International College of Angiology, IncCorkscrew Collateral Vessels in Buerger Disease: Vasa Vasorum or Vasa Nervorum.
Journal of vascular and interventional radiology : JVIRSmoking, Periodontitis, and Buerger Disease.
Annals of vascular surgeryEffect of a Low-Intensity Pulsed Ultrasound Device, SX-1001, on Clinical Symptoms in Buerger Disease With Limb Ischemia.
International heart journalThe Epidemiologic and Clinical Findings of Patients with Buerger Disease.
Annals of vascular surgeryOcular Inflammation in the Setting of Concomitant Systemic Autoimmune Conditions in an Older Male Population.
CorneaRefractory leg ulcers associated with Klinefelter syndrome.
Journal of Nippon Medical School = Nippon Ika Daigaku zasshiBuerger disease (thromboangiitis obliterans).
Techniques in vascular and interventional radiologyAssociações
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Referências e fontes
Bases de dados externas citadas neste artigo
Publicações científicas
Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.
- The Diagnostic Pitfall of Ankle-Brachial Index in Buerger Disease: Can We Trust Pressure Measurements in the Presence of Corkscrew Collaterals?
- A systematic review and meta-analysis of early and long-term outcomes after endovascular interventions in patients with thromboangiitis obliterans and critical limb ischemia with GRADE assessment.
- Seltoplasmid promotes ulcer healing versus placebo for treating patients with chronic limb-threatening ischemia: HOPE CLTI-2 trial.Molecular therapy : the journal of the American Society of Gene Therapy· 2025· PMID 40221835mais citado
- Treatment Options for Buerger Disease: A Systematic Review and Meta-Analysis of Outcomes.
- ANCA-Negative Pauci-Immune Crescentic Glomerulonephritis and Buerger Disease.Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases· 2025· PMID 39890210mais citado
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:36258(Orphanet)
- OMIM OMIM:211480(OMIM)
- MONDO:0008889(MONDO)
- GARD:5969(GARD (NIH))
- Busca completa no PubMed(PubMed)
- Artigo Wikipedia(Wikipedia)
- Q746001(Wikidata)
Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.
Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar
