دورية أكاديمية

A case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest pain

التفاصيل البيبلوغرافية
العنوان: A case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest pain
المؤلفون: BaÅŸkan, Merve, Akalın, Necdet, Ergin, Hacer, Gürses, Dolunay
سنة النشر: 2003
المجموعة: Pamukkale University Repository / Pamukkale Üniversitesi Açık Erişim Arşivi
مصطلحات موضوعية: polyarthritis, polymerase chain reaction, protein deficiency, rash, recurrent disease, Hereditary angioedema, C1 inhibitor deficiency, adrenalin, benzathine penicillin, complement component C1s inhibitor, danazol, diphenhydramine, salicylic acid, steroid, tranexamic acid, abdominal disease, adolescent, angioneurotic edema, article, autoimmune disease, case report, erythema, child care, diagnostic error, disease association, human, joint radiography, laboratory test, larynx edema, male
الوصف: Hereditary angioedema (HAE) results from a congenital deficiency of C1 inhibitor and is characterized by submucosal and subcutaneous edema of skin, larynx and abdomen. Occasional reports have appeared linking HAE with autoimmune diseases. We report a case of HAE presenting recurrent nondeforming polyarthritis, erythema marginatum-like rash and chest pain. There were no significant radiographic joint changes. Serologic tests for rheumatologic and autoimmune diseases were negative. After danazol treatment, physical examination and laboratory findings were normal over five years. We suggest that pediatricians should be aware of this rare disease and treat patients accordingly.
نوع الوثيقة: article in journal/newspaper
اللغة: English
ردمك: 978-0-00-187576-0
0-00-187576-0
تدمد: 0041-4301
العلاقة: Turkish Journal of Pediatrics; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; https://hdl.handle.net/11499/5239Test; 45; 261; 264; 2-s2.0-0242523152; WOS:000187576000016
الإتاحة: https://hdl.handle.net/11499/5239Test
حقوق: none
رقم الانضمام: edsbas.B522778D
قاعدة البيانات: BASE
الوصف
ردمك:9780001875760
0001875760
تدمد:00414301