Systemic mastocytosis may be primary or be associated with other hematological malignancies, most commonly myeloid neoplasms. In contrast, the association of systemic mastocytosis with lymphoid neoplasms is comparatively rare, and in the absence of appropriate clinical vigilance the diagnosis may be
Systemic antineutrophil cytoplasmic antibody vasculitis in a patient with chronic lymphocytic leukemia: Quite a rare diagnosis
✍ Scribed by Gülsüm Emel Pamuk; Mehmet Sevki Uyanık; Muzaffer Demir; Emre Tekgündüz; Burhan Turgut; Mehmet Soy
- Book ID
- 104040260
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 98 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0145-2126
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✦ Synopsis
There might be rheumatic manifestations of malignant diseases, especially those of the hematological type. Until now, antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis in chronic lymphocytic leukemia (CLL) has been reported on only very few occasions. Here, we present our patient with Rai stage II CLL who came to us with constitutional symptoms. She turned out to have hematuria with dysmorphic erythrocytes and developed hemoptysis. She had pulmonary-renal syndrome and was diagnosed with p-ANCA positive microscopic polyangiitis. She is currently using prednisolone and cyclophosphamide and undergoing regular hemodialysis. Constitutional symptoms in patients with hematological malignancies should make the physicians consider systemic vasculitis after exclusion of diseaserelated complications.
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