The coexistence of familial Mediterranean fever and polyarteritis nodosa; Report of a case

被引：20

作者：

Kocak, H ^{[1
]}

Cakar, N ^{[1
]}

Hekimoglu, B ^{[1
]}

Atakan, C ^{[1
]}

Akkok, N ^{[1
]}

Unal, S ^{[1
]}

机构：

[1] SOCIAL SECUR HOSP,DEPT PEDIAT NEPHROL,ANKARA,TURKEY

来源：

PEDIATRIC NEPHROLOGY | 1996年 / 10卷 / 05期

关键词：

familial Mediterranean fever; polyarteritis nodosa;

D O I：

10.1007/s004670050176

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

We describe a 14-year-old boy with a 5-year history of familial Mediterranean fever (FMF), treated with colchicine, who developed polyarteritis nodosa (PAN). He was admitted to our hospital with fever, general weakness, arthritis, and purpura. Five weeks after admission, hypertension was noted. Skin biopsy showed perivascular leukocyte infiltration in the epidermis. An aortography revealed multiple aneurysms of the renal, common hepatic, and intercostal arteries. He was treated with intravenous methylprednisolone, oral cyclophosphamide, and azathioprine. The known rare association of FMF and PAN is discussed.

引用

页码：631 / 633

页数：3

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