Eosinophilic Polymyositis in a Mouse

نویسنده

  • LISA A. KRUGNER-HIGBY
چکیده

CONTEMPORARY TOPICS © 1998 by the American Association for Laboratory Animal Science 94 The term eosinophilic myositis or polymyositis is used to describe a diverse, heterogeneous group of diseases in human beings and animals. One form of the disease may be associated with parasites that invade muscle tissue, such as Trichinella or Sarcocystis (1–4). In human beings, it has been described as a reaction to drugs (5) or nutritional supplements, as has occurred with particular suppliers of L-tryptophan (6, 7). Eosinophilic myositis also occurs as a disease of unknown origin (idiopathic eosinophilic polymyositis) (1, 8–12). In human beings, idiopathic eosinophilic myositis can occur as a localized lesion (9, 13) and has even been described as a pseudotumor (14), or as a generalized condition involving multiple skeletal muscles and the heart (8, 9, 11). The disease can occur with or without concurrent increase in the number of eosinophils in the peripheral blood (9, 11, 15). A form of idiopathic eosinophilic myositis has been described in dogs (16), in which the lesions are frequently confined to the muscles of mastication, but cases of generalized disease have also been described (16). This report describes a case of eosinophilic polymyositis involving skeletal as well as cardiac muscle in a mouse.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A Curious Case of Proximal Muscle Weakness with Eosinophilic Polymyositis

Eosinophilic polymyositis (EPM) is part of a rare disorder, eosinophilic myopathies (EM), which is a form of polymyositis characterized by the presence of eosinophils in muscle biopsy sections and occasionally blood eosinophilia. Herein, we are presenting an interesting case of eosinophilic polymyositis presenting with muscle pain with no other organ systems involved.

متن کامل

Severe Rhabdomyolysis without Systemic Involvement: A Rare Case of Idiopathic Eosinophilic Polymyositis

Introduction. Eosinophilic polymyositis (EPM) is a rare cause of rhabdomyolysis characterized by eosinophilic infiltrates in the muscle. We describe the case of a young patient with eosinophilic polymyositis causing isolated severe rhabdomyolysis without systemic involvement. Case Presentation. A 22-year-old Haitian female with no past medical history presented with progressive generalized musc...

متن کامل

Hypercapnic respiratory failure due to L-tryptophan-induced eosinophilic polymyositis.

A 24-year-old man presenting with fever, rash, and myalgias subsequently developed hypercapnic respiratory failure and severe limb muscle weakness. Muscle biopsy revealed eosinophilic myositis, due to the ingestion of large quantities of L-tryptophan as a dietary supplement. Complete recovery occurred with corticosteroid administration. Significant involvement of the respiratory muscles can be ...

متن کامل

Limb-girdle muscular dystrophy type 2B mimicking polymyositis.

Dr. Francisco de Assis Aquino Gondim – Universidade Federal do Ceará / CP 3157 Rua Cel Nunes de Melo 1127 60430-270 Fortaleza CE Brasil. E-mail: [email protected] Limb-girdle muscular dystrophy (LGMD) type 2B is caused by mutations in the dysferlin gene, located at cromossome 2p13.1-p13.3. This protein is normally expressed at the skeletal muscle, but in affected patients it is reduced or a...

متن کامل

Systemic sclerosis (scleroderma): specific autoantigen genes are selectively overexpressed in scleroderma fibroblasts.

The pathogenesis of systemic sclerosis (SSc) involves complex interactions between activated fibroblasts eventually leading to fibrosis, and impaired immune tolerance characterized by a variety of circulating SSc-specific autoantibodies. The expression of autoantigens in fibroblasts, a key target tissue in SSc, may play an important role in this process. To obtain a global view of this process,...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 1999