Autoimmune manifestations of the Wiskott-Aldrich syndrome
Seminars in Arthritis and Rheumatism, cilt.27, sa.4, ss.218-225, 1998 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 27 Sayı: 4
- Basım Tarihi: 1998
- Doi Numarası: 10.1016/s0049-0172(98)80002-4
- Dergi Adı: Seminars in Arthritis and Rheumatism
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.218-225
- Anahtar Kelimeler: Arthritis, Autoimmune disease, Colitis, Wiskott-Aldrich syndrome
- Maltepe Üniversitesi Adresli: Evet
Özet
Objective: To describe and review the autoimmune features and typical manifestations of Wiskott-Aldrich syndrome (WAS). Design: Case series and review of the literature. Setting: Tertiary care medical center and pediatric referral center. Patients: The presentation, diagnosis, and management of two cases are reported. In addition to the typical features of WAS, the first patient had hemolytic anemia, arthritis, leukocytoclastic vasculitis, and colitis. The second patient had colitis and arthralgias. Detailed review of features and therapeutic options in WAS as exemplified by these two patients are presented. Both patients had bone marrow transplantation, the only definitive treatment for WAS. Conclusions: WAS has variable clinical and autoimmune manifestations. Diagnosis must be suspected in a boy with small, decreased number of platelets and autoimmune problems or infections. Bone marrow transplantation is the only successful mode of treatment for all aspects of WAS.