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Comment on: Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd–Chiari syndrome and polyarteritis nodosa: reply

ASI Standing, D Eleftheriou, HJ Lachmann… - …, 2011 - Br Soc Rheumatology
Comment on: Familial Mediterranean fever caused by homozygous E148Q mutation complicated
by Budd Chiari syndrome and polyarteritis nodosa: reply SIR, We thank Konstantopoulos and
Kanta [1] for com- ments on our case report [2]. We agree that E148Q homo- zygosity ...
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Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd–Chiari syndrome and polyarteritis nodosa

ASI Standing, D Eleftheriou, HJ Lachmann… - …, 2011 - Br Soc Rheumatology
Sir, FMF is an inherited disorder characterized by recurrent episodes of fever accompanied by
sterile peritonitis, arthritis, pleuritis and a typical inflammatory rash [1]. The association between
FMF and mutations such as M694V, M694I and V726A has been clearly established [2]; ...
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ANCA-Associated Vasculitis, Churg Strauss syndrome, Polyarteritis Nodosa, and other vasculitic entities

R Müller… - Clinical Trials in Rheumatology, 2011 - Springer
Trial Treatment of Churg-Strauss syndrome without poor-prognosis factors: a multicenter,
prospective, randomized, open-label study of 72 patients Substance Corticosteroid therapy: Iv
pulse methylprednisolone (15 mg/kg, n = 72) Followed by oral prednisone (1 mg/kg/day) ...

A case of cutaneous polyarteritis nodosa (PAN) with no systemic involvement (초)

JY Shin, HS Jang… - 초록집, 2011 - papersearch.net
Eosinophilic fasciitis is a rare disorder with varying clinical presentations, making its clinical definition
challenging. It is a scleroderma-like syndrome that was first described in 1974 by Shulman in
patients with diffuse fasciitis and eosinophilia. Its onset is typically acute and findings ...

Hepatitis C virus–associated polyarteritis nodosa

D Saadoun, B Terrier, O Semoun… - Arthritis Care & …, 2011 - Wiley Online Library
Among a cohort of 161 patients with HCV-related vasculitis, 31 (19.3%) were diagnosed as having
PAN. The median age was 64.5 years (interquartile range 49.5–70.5 years), with 54.8%
women. Compared with HCV-associated mixed cryoglobulinemia (HCV-MC) vasculitis, ...
Cited by 1 - Related articles - All 3 versions

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