A case of myeloperoxidase-antineutrophil cytoplasmic antibody and anticardiolipin antibody-positive pyogenic arthritis, pyoderma gangrenosum, acne and hidradenitis suppurativa (PAPASH) syndrome with colitis

被引:3
|
作者
Kawanishi, Keishu [1 ]
Nishiwaki, Hiroki [1 ,2 ]
Oshiro, Tsuyoshi [1 ]
Kajitani, Hideto [1 ]
Amagasa, Masahito [1 ]
Uehara, Natsumi [3 ,4 ]
Inoue, Yoshihiko [5 ]
Nagahama, Masatsugu [4 ]
Koiwa, Fumihiko [1 ]
机构
[1] Showa Univ, Dept Internal Med, Div Nephrol, Fujigaoka Hosp, Yokohama, Kanagawa, Japan
[2] Showa Univ, Res Adm Ctr SURAC, Tokyo, Japan
[3] Med Topia Soka Hosp, Div Gastroenterol, Soka, Japan
[4] Showa Univ, Dept Internal Med, Div Gastroenterol, Fujigaoka Hosp, Yokohama, Kanagawa, Japan
[5] Showa Univ, Dept Internal Med, Div Rheumatol, Fujigaoka Hosp, Yokohama, Kanagawa, Japan
关键词
PAPA syndrome; inflammatory bowel disease; PAPASH syndrome; MPO-ANCA; anticardiolipin antibody; VASCULITIS; MUTATION; JAPAN;
D O I
10.1080/24725625.2021.1881216
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A previous case report of colitis and serine proteinase 3-antineutrophil cytoplasmic antibody positivity in pyogenic arthritis, pyoderma gangrenosum (PG), acne and hidradenitis suppurativa (PAPASH) syndrome with colitis has been published. Herein, we report a similar case of myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA) positivity. A 26-year-old man presented with recurrent aseptic pyogenic arthritis, acne, hidradenitis suppurativa and PG. Lower gastrointestinal endoscopy was performed, and colitis was observed. No PSTPIP1 gene mutation was found in the gene-sequencing test. Based on these findings and prior case reports, we diagnosed the patient with PAPASH syndrome, a PAPA spectrum disorder complicated by colitis. This patient had PAPASH syndrome with colitis and was MPO-ANCA and anticardiolipin antibodies-positive; it is unclear whether these antibodies play a role in this disease, but it may provide clues to further elucidate its pathogenesis.
引用
收藏
页码:333 / 336
页数:4
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