The Path to Diagnosis: Confirming Buerger Disease
At a Glance
Buerger disease is diagnosed by ruling out other conditions like diabetes or autoimmune disorders. Doctors use the Shionoya criteria, which requires a history of tobacco use and symptom onset before age 50. Diagnosis is confirmed through an angiogram showing distinctive "corkscrew" blood vessels.
Because there is no single blood test that can “prove” you have Buerger disease, doctors use a process called diagnosis of exclusion [1][2]. This means they must systematically rule out every other possible cause for your symptoms—such as diabetes, high cholesterol, or autoimmune diseases—before confirming it is Buerger disease. To do this, they rely on a specific set of clinical requirements and advanced imaging.
The Shionoya Diagnostic Criteria
Most specialists use the Shionoya criteria to determine if a patient has Buerger disease [3][4]. To receive a diagnosis, you typically must meet all five of these clinical benchmarks:
- Tobacco History: A current or recent history of using tobacco or nicotine products [3].
- Early Onset: The symptoms began before the age of 50 [3][4].
- Specific Blockages: Evidence of arterial blockages below the knee or elbow (infrapopliteal or infrabrachial) [3].
- Upper Limb or Vein Involvement: Signs of the disease in your hands/arms or a history of phlebitis migrans (migrating red lumps in the veins) [3].
- Exclusion of Others: No other major risk factors for atherosclerosis, such as uncontrolled diabetes or very high cholesterol [3][5].
Bedside Tests: Allen Test and ABI
Before ordering expensive scans, your doctor may perform simple physical tests:
- Allen Test: Your doctor will press on the arteries in your wrist and ask you to open and close your hand. When they release the pressure, they watch how quickly your palm turns red again. In Buerger disease, this process is often significantly slowed, indicating blockages in the small vessels of the hand [6][1].
- ABI (Ankle-Brachial Index): This test compares the blood pressure in your ankle to the blood pressure in your arm. While useful for checking general circulation, it can sometimes be misleading in Buerger disease because the blockages are often located much further down in the toes, where standard pressure cuffs cannot reach [7][8].
Imaging: “Corkscrew” Collaterals
The most definitive evidence of Buerger disease often comes from an angiogram—a special X-ray that uses dye to see inside your arteries [2].
- Segmental Occlusions: The scan will show “skip lesions,” where a section of an artery is blocked, followed by a healthy section, then another blockage [2][9].
- Corkscrew Collaterals: When an artery is blocked, the body tries to grow tiny new vessels to bypass it. In Buerger disease, these vessels have a very distinctive, wiggly appearance known as corkscrew collaterals [2][10]. While other diseases can cause collateral growth, this specific “corkscrew” pattern is a hallmark sign of TAO [2].
Your Diagnostic Checklist
To ensure your diagnosis is correct, your medical team should have performed the following to rule out other conditions:
- [ ] Blood Sugar & Lipids: To rule out diabetes and high cholesterol (atherosclerosis) [1].
- [ ] Autoimmune Panel: Tests like ANA (Antinuclear Antibody) and RF (Rheumatoid Factor) to rule out lupus or scleroderma [1].
- [ ] Echocardiogram: An ultrasound of the heart to ensure “traveling” blood clots (emboli) aren’t the cause [2][11].
- [ ] Hypercoagulable Screen: Tests to see if your blood has a genetic tendency to clot too easily [2].
- [ ] Vascular Imaging: A CTA, MRA, or traditional angiogram to look for the signature “corkscrew” vessels [2].
Common questions in this guide
How do doctors diagnose Buerger disease?
What are the Shionoya criteria for Buerger disease?
What does an Allen test check for?
What are corkscrew collaterals on an angiogram?
Why do I need an echocardiogram if Buerger disease affects my arms and legs?
Questions to Ask Your Doctor
Curated prompts to bring to your next appointment.
- 1.Do I meet all five of the Shionoya criteria, or are there 'atypical' features in my case?
- 2.What specific blood tests were run to rule out lupus, scleroderma, and other autoimmune conditions?
- 3.Did my imaging show 'corkscrew' collaterals, and if so, where are they located?
- 4.Has my heart been checked with an echocardiogram to make sure I don't have blood clots that could travel to my limbs?
- 5.Can you explain the results of my Allen test and how it reflects the blood flow to my fingers?
Questions For You
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References
References (11)
- 1
Recent Updates and Advances in Winiwarter-Buerger Disease (Thromboangiitis Obliterans): Biomolecular Mechanisms, Diagnostics and Clinical Consequences.
Fazeli B, Ligi D, Keramat S, et al.
Diagnostics (Basel, Switzerland) 2021; (11(10)) doi:10.3390/diagnostics11101736.
PMID: 34679434 - 2
[Thromboangiitis obliterans: an update 2025].
Stammler F
Deutsche medizinische Wochenschrift (1946) 2025; (150(23)):1440-1446 doi:10.1055/a-2660-1858.
PMID: 41213536 - 3
The Epidemiologic and Clinical Findings of Patients with Buerger Disease.
Igari K, Inoue Y, Iwai T
Annals of vascular surgery 2016; (30()):263-9.
PMID: 26370744 - 4
D-dimer levels in patients with thromboangiitis obliterans.
Emmanuel A, Selvaraj D, Sen I, et al.
The National medical journal of India 2019; (32(3)):134-136 doi:10.4103/0970-258X.278685.
PMID: 32129304 - 5
Application of nanofat grafting to rescue a severe ischaemic hand with thromboangiitis obliterans: A case report about promising salvage procedure.
Ng KLB, Hsieh MW, Lin YN, et al.
Medicine 2021; (100(42)):e27577 doi:10.1097/MD.0000000000027577.
PMID: 34678903 - 6
Pathogenesis and Management of Buerger's Disease.
Liew NC, Lee L, Nor Hanipah Z, et al.
The international journal of lower extremity wounds 2015; (14(3)):231-5 doi:10.1177/1534734615599654.
PMID: 26264874 - 7
Clinical outcomes in patients with infrapopliteal arterial occlusive disease treated by lower extremity bypass surgery: a comparison of atherosclerosis and thromboangiitis obliterans.
Yan K, Yuan ZH, Zheng Y, Wang J
European review for medical and pharmacological sciences 2022; (26(12)):4228-4237 doi:10.26355/eurrev_202206_29059.
PMID: 35776021 - 8
Autologous bone marrow-derived mononuclear cell therapy in Chinese patients with critical limb ischemia due to thromboangiitis obliterans: 10-year results.
Guo J, Guo L, Cui S, et al.
Stem cell research & therapy 2018; (9(1)):43 doi:10.1186/s13287-018-0784-6.
PMID: 29471870 - 9
Buerger Disease: Pathological Changes in Elderly Patients.
Iwai T, Kume H, Koizumi S, et al.
Annals of vascular diseases 2022; (15(1)):29-36 doi:10.3400/avd.oa.21-00142.
PMID: 35432646 - 10
Corkscrew Collateral Vessels in Buerger Disease: Vasa Vasorum or Vasa Nervorum.
Baş A, Dikici AS, Gülşen F, et al.
Journal of vascular and interventional radiology : JVIR 2016; (27(5)):735-9.
PMID: 27013404 - 11
A Non-smoking Woman with Anti-phospholipid Antibodies Proved to Have Thromboangiitis Obliterans.
Shima N, Akiyama Y, Yamamoto S, et al.
Internal medicine (Tokyo, Japan) 2020; (59(3)):439-443 doi:10.2169/internalmedicine.3372-19.
PMID: 31588083
This page provides educational information about diagnostic tests and criteria for Buerger disease. It does not replace professional medical advice from your vascular specialist or healthcare provider.
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