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Polyarteritis Nodosa (0)
Articles on Polyarteritis Nodosa
The Five-Factor Score revisited: assessment of prognoses of systemic necrotizing vasculitides based on the French Vasculitis Study Group (FV...
We revisited the FFS, this time including Wegener granulomatosis (WG).We analyzed clinical, laboratory, and immunologic manifestations present at diagnosis of systemic necrotizing vasculitides for 1108 consecutive patients registered in the French Vasculitis Study Group database. All patients met th...
Use of warfarin therapy at a target international normalized ratio of 3.0 for cutaneous polyarteritis nodosa
We have previously suggested that CPN might be associated with the presence of anti-phosphatidylserine-prothrombin complex (anti-PS/PT) antibodies, members of the antiphospholipid antibody family. To evaluate clinical manifestations and effective treatments of CPN. We...
Pulmonary hypertensive necrotizing arteritis: An unusual case of unilateral involvement in an infant with congenital heart disease
We report a unique case of an infant with congenital heart disease causing pulmonary hypertension and necrotizing pulmonary arteritis but affecting only one lung. In conclusion, in pulmonary valve atresia, the lungs may be supplied via aortopulmonary collaterals. Necrotizing pulmonary arteritis is a...
A case of systemic polyarteritis nodosa involving bronchial artery.
We report a case of PAN with initial presentation of hemoptysis. On admission, chest radiograph and chest CT angiography revealed no focus of bleeding. Angiography showed a bronchial artery aneurysm and multiple arterial aneurysms in both renal, hepatic, mesenteric and branches of small bowel arteri...
[Childhood cutaneous polyarteritis nodosa].
Cutaneous polyarteritis nodosa is an infrequent necrotizing vasculitis of small and medium-sized arteries, with a recurrent and chronic course, that can be associated with fever, arthralgia, myalgia and neuropathy without visceral involvement. We report a cutaneous polyarteritis nodosa case.
Case 2-2010: a man with abdominal and flank pain.
An old autopsy report sheds light on a "new" disease: infantile polyarteritis nodosa and kawasaki disease.
Although Kawasaki disease (KD) was first discovered and identified in Japan by Kawasaki in the 1960s, fatal KD cases resulting from coronary artery aneurysms had been identified retrospectively in the West as early as 1871. Kawasaki initially postulated that this disease was a new, as yet unidentifi...
A patient with hepatitis B, liver and kidney dysfunction and polyneuropathy.
[Case of isolated polyarteritis nodosa appearing in bilateral epididymis].
We performed bilateral high orchiectomy. Pathological examination shows necrotizing vasculaitis surrounded by glanulomas and pathologically diagnosed as Polyarteritis Nodosa in bilateral epididymis. After orchiectomy, blood examination of immunity was revealed no specific findings, that made us diag...
Testicular polyarteritis nodosa mimicking testicular neoplasm.