Polyarteritis nodosa with gallbladder involvement is a rare condition. Autosomal dominant polycystic kidney disease is also a rare condition and rarely complicated. We describe an extremely rare case of Polyarteritis nodosa, involving gallblader and ureter without obstruction, in a patient with autosomal dominant polycystic kidney disease. To the best of the authors’ knowledge, such a case has ...

POLYARTERITIS NODOSA is a disease in which widespread acute necrosis occurs in the arteries, leading to a variety of functional disturbances involving the nervous system, heart, kidneys, lungs, abdominal viscera, and blood (Harvey, 1959). The liver is affected in this condition more frequently than is recognized. The following case report illustrates the need for care in the administration of m...

We report a case of bilateral ureteral obstruction most likely caused by polyarteritis nodosa. The diagnosis was based upon muscle biopsy which showed typical necrotizing vasculitis in medium size artery in conjunction with microaneurysms in renal angiography. Ureteral obstruction is a rare manifestation of polyarteritis nodosa. This condition is thought to result from vasculitis of periuretera...

Polyarteritis nodosa (PAN) is a systemic vasculitis whose severe forms are treated with glucocorticoids and cyclophosphamide. Refractory patients are exposed to many complications, notably accelerated atherosclerosis. We report a case report of 71-year-old man followed for polyarteritis nodosa refractory to glucocorticoids and cyclosphosphamide. Systemic vasculitis relapses are followed to acce...

Polyarteritis nodosa is multisystem disease with necrotizing vasculitis of middle and small sized arteries. Takayasu arteritis is a rare nonspecific inflammatory disease with unknown cause, predominantly affecting the aorta and its main branches. In the literature, experience about the appropriate graft selection and the long-term patency is reported for vasculitis syndromes such as Takayasu’s ...