Cutaneous Polyarteritis Nodosa as the Inaugural Manifestation of Hairy Cell Leukemia
n/a.
Filipe Monteiro +4 more
doaj +1 more source
Burn Center Management of Severe Necrotic Cutaneous Polyarteritis Nodosa in a Patient With a History of Thymoma. [PDF]
Abousy M +4 more
europepmc +1 more source
Cutaneous polyarteritis nodosa. [PDF]
D A Fitzgerald, J L Verbor
openaire +3 more sources
An IVF-Twin Pregnancy Complicated with Cutaneous Polyarteritis Nodosa: A Case Report
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
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
Development of Arthritis as the Initial Involvement in Adult-Onset Cutaneous Polyarteritis Nodosa: Two Cases and Literature Review. [PDF]
Takamatsu R +5 more
europepmc +1 more source
[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.
Matías F, Stringa +6 more
openaire +1 more source
Epidemiology of Vasculitides in Khorasan Province, Iran
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.
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
Molecular evidence of parvovirus B19 in the cutaneous polyarteritis nodosa tissue from a patient with parvovirus-associated hemophagocytic syndrome: Case report. [PDF]
Jeong JY +4 more
europepmc +1 more source

