Hemocholecyst complicated in a hemodialysis patient with microscopic polyangiitis
著者
丸山, 啓介
(Maruyama, Keisuke)
中川, 直樹
(Nakagawa, Naoki)
鹿原, 真樹
(Kabara, Maki)
珍田, 純子
(Chinda, Junko)
藤野, 貴行
(Fujino, Takayuki)
長谷部, 直幸
(Hasebe, Naoyuki)
上位タイトル
Modern rheumatology
(2015.
3)
,p.1-
4
識別番号
ISSN
1439-7595
DOI
10.3109/14397595.2015.1016138
その他
PMID：25671404
抄録
Microscopic polyangiitis (MPA) is a systemic vasculitis associated with antineutrophil cytoplasmic antibodies, and it involves multiple organs, including the kidneys and lungs. We report on the case of a 72-year-old woman with MPA who developed hemocholecyst in addition to alveolar hemorrhage and rapidly progressive glomerulonephritis. Although her renal function was not salvaged, the alveolar hemorrhage and hemocholecyst were treated conservatively. Clinicians should consider the possibility of hemocholecyst in patients with MPA complaining of abdominal pain.
