Muscular polyarteritis nodosa-a case-based review

被引:0
|
作者
Krusche, M. [1 ]
Ruffer, N. [1 ]
Kubacki, T. [1 ]
Matschke, J. [2 ]
Koetter, I. [1 ]
机构
[1] Asklepios Klin Altona, Nephrol, Rheumatol, Klin Immunol, Paul Ehrlich Str 1, D-22763 Hamburg, Germany
[2] Univ Klinikum Hamburg Eppendorf, Inst Neuropathol, Hamburg, Germany
来源
ZEITSCHRIFT FUR RHEUMATOLOGIE | 2019年 / 78卷 / 02期
关键词
Creatine kinase; Vasculitis; Myalgia; Myositis; Muscle biopsy; MUSCLE INVOLVEMENT; BIOPSY;
D O I
10.1007/s00393-019-0595-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundMyalgia is acommon but unspecific set of symptoms that may be caused by orthopedic, neurological and internal medical conditions, often resulting in a diagnostic challenge. Muscular polyarteritis nodosa (PAN) is arare differential diagnosis of myalgia with elevated serological inflammatory markers.ObjectiveBased on three clinical cases and the literature this review describes the essential clinical and diagnostic features of muscular PAN.ResultsMuscular PAN typically presents with immobilizing myalgia confined to the lower limbs and elevated serological inflammatory markers but often normal creatine kinase (CK) levels. Contrast-enhanced magnetic resonance imaging of the affected muscles, which can often mimic myositis, and muscle biopsy provide the relevant histological findings that lead to the diagnosis of a vasculitis.ConclusionWith respect to own experiences and the reviewed literature, muscular PAN should be considered as apossible diagnosis in cases of myalgia with elevated inflammatory markers but normal CK levels and a lack of further symptoms typical for vasculitis.
引用
收藏
页码:173 / 179
页数:7
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