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 not been reported previously. "Una Manifestación poco usual de la Poliarteritis Nodosa Reporte de un Caso" La periarteritis nodosa con compromiso de la vesícula es una condición rara. La enfermedad poliquística renal autosómica dominante es también una condición rara y raramente complicada. Describimos un caso extremadamente raro de poliarteritis ...
In the medical literature, there have been few reported cases of classic Polyarteritis Nodosa (cPAN)...
The authors report a rare case of an acalculous gangrenous cholecystitis due to a form of vasculitis...
Polyarteritis nodosa (PAN) is a systemic vasculitis of unknown etiology. Although gastrointestinal i...
International audienceRenal involvement of systemic vasculitides is an emergency in nephrology. Alth...
Classic polyarteritis nodosa (cPAN) is a systemic necrotizing vasculitis of medium-sized muscular ar...
IntroductionAutosomal Dominant Polycystic Kidney Disease (ADPKD) is a multisystemic disorder charact...
Autosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal ...
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects the medium- and small-s...
Polyarteritis nodosa (PAN) is a necrotizing inflammatory vasculitis of small-and medium-sized muscul...
Se presentó un enfermo con poliarteritis nodosa cuyo diagnóstico se sustentó en aspectos clínicos, h...
The objective of the present study was to determine the frequency of the most common clinical featur...
Introduction: Polyarteritis Nodosa (PAN) is a systemic vasculitis affecting small and medium size ar...
Polyarteritis nodosa (PAN) of the urinary tract is rare. An unusual case of systemic PAN involving t...
This is an open access article published under the Creative Commons CC-BY-NC 3.0 license
Objectives. Polyarteritis nodosa (PAN) is a term that has been used to describe a wide variety of va...
In the medical literature, there have been few reported cases of classic Polyarteritis Nodosa (cPAN)...
The authors report a rare case of an acalculous gangrenous cholecystitis due to a form of vasculitis...
Polyarteritis nodosa (PAN) is a systemic vasculitis of unknown etiology. Although gastrointestinal i...
International audienceRenal involvement of systemic vasculitides is an emergency in nephrology. Alth...
Classic polyarteritis nodosa (cPAN) is a systemic necrotizing vasculitis of medium-sized muscular ar...
IntroductionAutosomal Dominant Polycystic Kidney Disease (ADPKD) is a multisystemic disorder charact...
Autosomal dominant polycystic kidney disease is a common hereditary disorder characterized by renal ...
Polyarteritis nodosa (PAN) is a systemic necrotizing vasculitis that affects the medium- and small-s...
Polyarteritis nodosa (PAN) is a necrotizing inflammatory vasculitis of small-and medium-sized muscul...
Se presentó un enfermo con poliarteritis nodosa cuyo diagnóstico se sustentó en aspectos clínicos, h...
The objective of the present study was to determine the frequency of the most common clinical featur...
Introduction: Polyarteritis Nodosa (PAN) is a systemic vasculitis affecting small and medium size ar...
Polyarteritis nodosa (PAN) of the urinary tract is rare. An unusual case of systemic PAN involving t...
This is an open access article published under the Creative Commons CC-BY-NC 3.0 license
Objectives. Polyarteritis nodosa (PAN) is a term that has been used to describe a wide variety of va...
In the medical literature, there have been few reported cases of classic Polyarteritis Nodosa (cPAN)...
The authors report a rare case of an acalculous gangrenous cholecystitis due to a form of vasculitis...
Polyarteritis nodosa (PAN) is a systemic vasculitis of unknown etiology. Although gastrointestinal i...