Results 71 to 80 of about 2,648 (158)

Cutaneous Polyarteritis Nodosa as the Inaugural Manifestation of Hairy Cell Leukemia

open access: yesActa Médica Portuguesa
n/a.
Filipe Monteiro   +4 more
doaj   +1 more source

Cutaneous polyarteritis nodosa. [PDF]

open access: yesArchives of Disease in Childhood, 1996
D A Fitzgerald, J L Verbor
openaire   +3 more sources

An IVF-Twin Pregnancy Complicated with Cutaneous Polyarteritis Nodosa: A Case Report

open access: yesGynecology Obstetrics & Reproductive Medicine, 2007
A twin pregnancy after the Assisted Reproductive Technology (ART) complicated with cutaneous polyarteritis nodosa (PAN) is presented. A 28-years-old, nulliparous woman developed cutaneous PAN four years before the IVF-pregnancy.
Namık Kemal Duru   +7 more
doaj  

IgA vasculitis associated with chronic myelomonocytic leukemia

open access: yesBMC Rheumatology
IgA vasculitis is a predominantly pediatric autoimmune disease characterized by IgA deposit in small vessels. Chronic myelomonocytic leukemia (CMML) is a rare hematological malignancy classified within myelodysplastic syndromes.
Bénédicte Rouvière   +6 more
doaj   +1 more source

[Childhood cutaneous polyarteritis nodosa].

open access: yesArchivos argentinos de pediatria, 2010
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.
Matías F, Stringa   +6 more
openaire   +1 more source

Epidemiology of Vasculitides in Khorasan Province, Iran

open access: yesIranian Journal of Medical Sciences, 2015
Vasculitides are a heterogeneous group of more than 20 diseases defined by inflammation and destruction of blood vessels. We aimed to study the demographic characteristics of the primary vasculitides in the North East of Iran.
Mohammadhassan Jokar, Zahra Mirfeizi
doaj  

Prognosis of cutaneous polyarteritis nodosa.

open access: yesCanadian family physician Medecin de famille canadien, 2013
A 17-year-old girl had cutaneous polyarteritis nodosa (CPN) of four years' duration. She had no clinical or laboratory evidence of associated systemic disease but was concerned about whether the CPN would remain cutaneous. Her case is reviewed in the context of previously reported cases.
J B, McKendry, M J, Phillips
openaire   +1 more source

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