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Peripheral Ischemia and Necrosis Revealing Buerger's Disease in an Internal Medicine Department

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Buerger's disease is a systemic vasculitis strongly correlated with tobacco use. It entails a heavy socio-occupational impact. We report the case of a 26-year-old patient with ischemia of the lower limbs revealing Buerger’s disease. He is known smoker with passive exposure to Indian hemp. He was seen for ischemic foot pain that had been progressing for a year. Involvement began in the left big toe. Subsequently, hyperalgesic necrotic lesions were observed on the 3rd, 4th and 5th toes of the foot. Biological investigations revealed an inflammatory syndrome with normocytic anemia and increased C-reactive protein. Retroviral, syphilitic, Hepatitis B and C viruses and SARS-CoV-2 serologies were negative. Antinuclear antibodies were initially borderline at 100 IU with speckled fluorescence, then negative on control. Neutrophil cytoplasmic antibodies and antiphospholipid antibodies were negative. Investigation of thrombophilia was non-contributory, notably factor V mutation testing, antithrombin III assay, proteins C and S and fibrinogen. An arterial ultrasound revealed extensive arterial thrombosis with thickening of the femoral arterial vessel walls. Thromboangiitis obliterans was confirmed and the patient was put on corticosteroids and adjuvant therapy. Surgical treatment was performed 4 months later. Buerger's disease is a serious vascular disorder which must be diagnosed very early in order to prevent complications. Early smoking cessation leads to remission in the early phase.
Title: Peripheral Ischemia and Necrosis Revealing Buerger's Disease in an Internal Medicine Department
Description:
Buerger's disease is a systemic vasculitis strongly correlated with tobacco use.
It entails a heavy socio-occupational impact.
We report the case of a 26-year-old patient with ischemia of the lower limbs revealing Buerger’s disease.
He is known smoker with passive exposure to Indian hemp.
He was seen for ischemic foot pain that had been progressing for a year.
Involvement began in the left big toe.
Subsequently, hyperalgesic necrotic lesions were observed on the 3rd, 4th and 5th toes of the foot.
Biological investigations revealed an inflammatory syndrome with normocytic anemia and increased C-reactive protein.
Retroviral, syphilitic, Hepatitis B and C viruses and SARS-CoV-2 serologies were negative.
Antinuclear antibodies were initially borderline at 100 IU with speckled fluorescence, then negative on control.
Neutrophil cytoplasmic antibodies and antiphospholipid antibodies were negative.
Investigation of thrombophilia was non-contributory, notably factor V mutation testing, antithrombin III assay, proteins C and S and fibrinogen.
An arterial ultrasound revealed extensive arterial thrombosis with thickening of the femoral arterial vessel walls.
Thromboangiitis obliterans was confirmed and the patient was put on corticosteroids and adjuvant therapy.
Surgical treatment was performed 4 months later.
Buerger's disease is a serious vascular disorder which must be diagnosed very early in order to prevent complications.
Early smoking cessation leads to remission in the early phase.

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