Allergic granulomatosis and angiitis in the absence of asthma and blood eosinophilia: A rare presentation of limited Churg-Strauss syndrome

Sevinc, Alper; HASANOĞLU, HATİCE; Gokirmak, Munire; Yildirim, Zeki; Baysal, Tamer; Mizrak, Bulent

doi:10.1007/s00296-003-0412-2

Allergic granulomatosis and angiitis in the absence of asthma and blood eosinophilia: A rare presentation of limited Churg-Strauss syndrome

Sevinc A., HASANOĞLU H. C., Gokirmak M., Yildirim Z., Baysal T., Mizrak B.

Rheumatology International, cilt.24, sa.5, ss.301-304, 2004 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 24 Sayı: 5
Basım Tarihi: 2004
Doi Numarası: 10.1007/s00296-003-0412-2
Dergi Adı: Rheumatology International
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.301-304
Anahtar Kelimeler: Asthma, Churg-Strauss syndrome, Eosinophilia
Ankara Yıldırım Beyazıt Üniversitesi Adresli: Hayır

Özet

Allergic granulomatosis and angiitis, also known as Churg-Strauss syndrome (CSS), is an uncommon vasculitis of unknown etiology. We report a 21-year-old male patient with fatigue, dry cough, and progressive dyspnea. He had no history of asthma or eosinophilia. Thorax computed tomography showed bullous/cystic areas with thin walls in varying sizes (5-15 mm). Histopathological examination of the open lung biopsy revealed granulomatous infiltration with histiocytes and eosinophilic leukocytes. This extremely rare variant of CSS is discussed.