Non-thrombocytopenic purpura in familial Mediterranean fever—comorbidity with Henoch–Schönlein purpura or an additional rare manifestation of familial Mediterranean fever?: Table 1

Rheumatology ◽  
2015 ◽  
Vol 55 (7) ◽  
pp. 1153-1158 ◽  
Author(s):  
Eldad Ben-Chetrit ◽  
Hasan Yazici
Keyword(s):  
Familial Mediterranean Fever ◽  
Henoch Schonlein Purpura ◽  
Thrombocytopenic Purpura ◽  
Rare Manifestation ◽  
Mediterranean Fever ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

Cerebral vasculitis in a child with Henoch–Schönlein purpura and familial Mediterranean fever

2007 ◽  
Vol 26 (10) ◽  
pp. 1729-1732 ◽  
Author(s):  
Ozan Özkaya ◽  
Kenan Bek ◽  
Neşe Alaca ◽  
Meltem Ceyhan ◽  
Yonca Açıkgöz ◽  
...  
Keyword(s):  
Familial Mediterranean Fever ◽  
Cerebral Vasculitis ◽  
Henoch Schonlein Purpura ◽  
Mediterranean Fever ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

MEFV Mutations Modify the Clinical Presentation of Henoch-Schönlein Purpura

2008 ◽  
Vol 35 (12) ◽  
pp. 2427-2429 ◽  
Author(s):  
Z. BÝRSÝN ÖZÇAKAR ◽  
FATOS YALÇINKAYA ◽  
NÝLGÜN ÇAKAR ◽  
BANU ACAR ◽  
ÖZGÜR KASAPÇOPUR ◽  
...  
Keyword(s):  
Mutation Analysis ◽  
Clinical Presentation ◽  
Gene Mutations ◽  
Henoch Schonlein Purpura ◽  
Reactive Protein ◽  
Mefv Mutations ◽  
Mediterranean Fever ◽  
Turkish Patients ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

ObjectiveTo investigate the prevalence of MEFV gene mutations in Turkish patients with Henoch-Schönlein purpura (HSP) but with no symptoms of familial Mediterranean fever (FMF). In addition, we assessed the clinical and laboratory characteristics of HSP patients with and without MEFV mutations.MethodsEighty pediatric patients with HSP (44 boys and 36 girls) were enrolled. Blood for mutation analysis was obtained either at the time of the diagnosis of HSP or during followup visits in previously diagnosed patients. No patient had the diagnosis of FMF in their history and in the followup period. Exon 10 of the MEFV gene was screened, together with p.E148Q mutation analysis.ResultsTwenty-seven (34%) patients were found to be heterozygous for one of the screened MEFV mutations; p.M694V in 16, p.M680I in 5, p.V726A in 3, and p.E148Q in 3 patients. Patients with MEFV mutations were younger than those without mutations and they had edema and arthritis more frequently. Also, the frequencies of elevated erythrocyte sedimentation rate and C-reactive protein values were found to be significantly higher in patients who had MEFV mutations.ConclusionAlterations in the MEFV gene are important susceptibility factors for the development of HSP and also affect the clinical presentation of it.

scholarly journals A challenging case on diagnosing Henoch–Schönlein purpura

2020 ◽  
Vol 18 ◽  
pp. 205873922092958
Author(s):  
Lin-Hao Zhang ◽  
Tian Lan ◽  
Du He ◽  
Shi-Lei Wen ◽  
Huan Tong
Keyword(s):  
Abdominal Pain ◽  
Gastrointestinal Tract ◽  
The Elderly ◽  
Henoch Schonlein Purpura ◽  
Thrombocytopenic Purpura ◽  
Multiple Organs ◽  
First Onset ◽  
Schonlein Purpura ◽  
Henoch Schönlein Purpura

Henoch–Schönlein purpura (HSP) could involve multiple organs, including gastrointestinal tract. It is commonly observed in children, but occasionally also in the elderly. It is challenging to diagnose HSP with delayed purpura. Herein, we report an elderly with HSP, whose non-thrombocytopenic purpura erupted more than 1 month after the first onset of abdominal pain.

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