1. Antineutrophil cytoplasmic antibody-associated vasculitis involving diffuse alveolar hemorrhage, rapidly progressive glomerulonephritis and hypereosinophilia
- Author
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Hirofumi Kamata, Atsushi Chiyotani, Naoki Hasegawa, Koichi Sayama, Makio Mukai, Yasuhiro Okubo, Hiroyoshi Kunimoto, and Hidefumi Koh
- Subjects
Adult ,Pathology ,medicine.medical_specialty ,Hypereosinophilia ,Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis ,Hemorrhage ,urologic and male genital diseases ,Glomerulonephritis ,immune system diseases ,Hypereosinophilic Syndrome ,Internal Medicine ,medicine ,Rapidly progressive glomerulonephritis ,Humans ,Anti-neutrophil cytoplasmic antibody ,Lung ,Hypereosinophilic syndrome ,business.industry ,Diffuse alveolar hemorrhage ,General Medicine ,medicine.disease ,respiratory tract diseases ,Pulmonary Alveoli ,medicine.anatomical_structure ,Disease Progression ,Female ,medicine.symptom ,business ,Vasculitis - Abstract
The classification of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) has limitations because the condition includes disorders with similar general clinical features, similar characteristics of lung and renal involvement and a positive ANCA serology. A 40-year-old woman was admitted to our hospital for hemoptysis and dyspnea. She had no history of bronchial asthma. Laboratory examinations revealed hypereosinophilia, positive anti-myeloperoxidase antibodies, hematuria and proteinuria. The patient was ultimately diagnosed with AAV associated with diffuse alveolar hemorrhage, rapidly progressive glomerulonephritis and hypereosinophilia without bronchial asthma. Obtaining a definitive diagnosis of ANCA vasculitis can be very difficult, and the characteristics of this case were not compatible with the findings of typical AVV. We herein report a rare case of AVV.
- Published
- 2013