Buerger's disease

Infobox_Disease
Name = Buerger's disease


Caption =
DiseasesDB = 1762
ICD10 = ICD10|I|73|1|i|70
ICD9 = ICD9|443.1
ICDO =
OMIM = 211480
MedlinePlus =
eMedicineSubj = med
eMedicineTopic = 253
MeshName = Thromboangiitis+Obliterans
MeshNumber = C14.907.137.870
:"Not to be confused with Berger's disease (IgA nephropathy)"

Buerger's disease (also known as "thromboangiitis obliterans") is an acute inflammation and thrombosis (clotting) of arteries and veins of the hands and feet. It is strongly associated with use of tobacco products, [cite journal | author=Joyce JW | title=Buerger's disease (thromboangiitis obliterans) | journal=Rheum Dis Clin North Am | year=1990 | pages=463–70 | volume=16 | issue=2 | pmid=2189162 ] primarily from smoking, but also from smokeless tobacco.

Features

There is a recurrent acute and chronic inflammation and thrombosis of arteries and veins of the hands and feet. The main symptom is pain in the affected areas. Ulcerations and gangrene in the extremities are common complications, often resulting in the need for amputation of the involved extremity.

Diagnosis

A concrete diagnosis of thromboangiitis obliterans is often difficult as it relies heavily on exclusion of the conditions. The commonly followed diagnostic criteria are below although the criteria tend to differ slightly from author to author. Olin (2000) proposes the following criteria: [Olin JW. "Thromboangiitis obliterans (Buerger's disease)." N Engl J Med 2000;343:864-9. PMID 10995867.]
# Age younger than 45 years
# Current (or recent) history of tobacco use
# Presence of distal extremity ischemia (indicated by claudication, pain at rest, ischemic ulcers or gangrene) documented by noninvasive vascular testing such as ultrasound
# Exclusion of other autoimmune diseases, hypercoagulable states, and diabetes mellitus by laboratory tests.
# Exclusion of a proximal source of emboli by echocardiography and arteriography
# Consistent arteriographic findings in the clinically involved and noninvolved limbs.

Pathophysiology

There are characteristic pathologic findings of acute inflammation and thrombosis (clotting) of arteries and veins of the hands and feet (the lower limbs being more common). The mechanisms underlying Buerger's disease are still largely unknown. It is suspected that immunological reactions play a role.

Treatment

Symptoms are treated as there is no treatment for the disease. Cessation of tobacco use may slow any further progression of the disease. Vascular surgery can sometimes be helpful in treating limbs with poor perfusion secondary to this disease. Use of vascular growth factor and stem cell injections have been showing promise in clinical studies.

Streptokinase has been proposed as adjuvant therapy in some cases.cite journal |author=Hussein EA, el Dorri A |title=Intra-arterial streptokinase as adjuvant therapy for complicated Buerger's disease: early trials |journal=International surgery |volume=78 |issue=1 |pages=54–8 |year=1993 |pmid=8473086 |doi=]

Prognosis

Buerger's is not immediately fatal, but life-shortening. Amputation is common and major amputations (of limbs rather than fingers/ toes) are almost twice as common in patients who continue to smoke. Death rate has not been consistently shown as higher in patients who do not cease smoking but for this and other health concerns quitting is highly recommended. Female patients tend to show much higher longevity rates than men.

Prevention

The cause of the disease is unknown but thought to be autoimmune in nature and heavily linked to tobacco use. There have also been links to persons with digestive disorders.

Epidemiology

Buerger's is more common among men than women. It is more common in Israel, Japan and India along the "old silk route" than in the United States and Europe. The disease is most common among South Asians.

History

Buerger's disease was first reported by Felix von Winiwarter in 1879 in Austria. [von Winiwarter F: Ueber eine eigenthumliche Form von Endarteriitis und Endophlebitis mit Gangran des Fusses. Arch Klin Chir 1879; 23: 202-26.]

It wasn't until 1908, however, that the disease was given its first accurate pathological description, by Leo Buerger at Mount Sinai Hospital in New York City. [Buerger L. "Thrombo-angiitis obliterans: a study of the vascular lesions leading to presenile spontaneous gangrene." Am J Med Sci 1908;136:567-80.] Buerger called it "presenile spontaneous gangrene" after studying amputations in 11 patients.

References

External links

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* [http://www.brandoncarmichael.com/ Brandon Carmichael]