| 영문 | sarcoidosis | 한글 | 사코이드증 |
|---|---|---|---|
| 설명 | 만성적이고 진행적인 육아종성 염증으로 인체 내의 모든 조직이나 장기를 침범할 수 있다. 조직학적으로는 비치즈성 상피모양세포 증식이 특징이다. |
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| DM | 1) Diabetes Mellitus 2) Dermato-Myositis |
|---|---|
| IBM | inclusion body myositis |
| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
| BREASTS | bronchopulmonary aspergillosis, radiotherapy, extrinsic allergic alveolitis, ankylosing spondylitis,... |
| SA | salicylic acid; saline [solution]; salt added; sarcoidosis; sarcoma; scalenus anticus; secondary ame... |
| IBM | Inclusion body myositis |
|---|---|
| SA | Sarcoidosis |
| S-IBM | Sporadic inclusion body myositis |
| SAR | sarcoidosis |
| sarcoidosis | <disease> Disease of unknown aetiology in which there are chronic inflammatory granulomatous lesions in lymph nodes and other organs. (18 Nov 1997) |
|---|---|
| sarcoidosis, pulmonary | Sarcoidosis affecting predominantly the lungs, the site most frequently involved and most commonly causing morbidity and mortality in sarcoidosis. Pulmonary sarcoidosis is characterised by sharply circumscribed granulomas in the alveolar, bronchial, and vascular walls, composed of tightly packed cells derived from the mononuclear phagocyte system. The clinical symptoms when present are dyspnea upon exertion, nonproductive cough, and wheezing. (cecil textbook of medicine, 19th ed, p431) (12 Dec 1998) |
| pulmonary sarcoidosis | <radiology> Stage, I hilar/mediastinal lymph nodes, II nodes and lung disease, III lung disease only, upper lobe predominance, superinfection with Aspergillus (investigate with thin-cut CT) See: sarcoidosis (12 Dec 1998) |
| acute disseminated myositis | The occurrence of multiple foci of acute inflammation in the muscular tissue and overlying skin in various parts of the body, accompanied by fever and other signs of systemic infection. See: dermatomyositis. Synonym: acute disseminated myositis, pseudotrichinosis, pseudotrichiniasis. (05 Mar 2000) |
| cervical myositis | See: posttraumatic neck syndrome. (05 Mar 2000) |
| multiple myositis | The occurrence of multiple foci of acute inflammation in the muscular tissue and overlying skin in various parts of the body, accompanied by fever and other signs of systemic infection. See: dermatomyositis. Synonym: acute disseminated myositis, pseudotrichinosis, pseudotrichiniasis. (05 Mar 2000) |
| myositis | <pathology> Inflammation of a voluntary muscle. Origin: Gr. Myos = of muscle (18 Nov 1997) |
| myositis fibrosa | Induration of a muscle through an interstitial growth of fibrous tissue. Synonym: Froriep's induration, interstitial myositis, myofascitis. (05 Mar 2000) |
| myositis, inclusion body | A progressive inflammatory myopathy primarily involving muscles of the pelvic region and legs, usually seen in older people. The muscles are infiltrated by mononuclear inflammatory cells, sarcoplasmic vacuoles, masses of filaments and filamentous microtubules, and sometimes eosinophilic bodies. (12 Dec 1998) |
| myositis ossificans | A disease characterised by bony deposits or the ossification of muscle tissue. (12 Dec 1998) |
| myositis ossificans circumscripta | Local deposit of bone in a muscle, usually following prolonged trauma; e.g., riders' bone. (05 Mar 2000) |
| myositis ossificans progressiva | <radiology> Progressive skeletal fusion, ossification of ligaments, nuchal ligament, pelvic entheses, asymptomatic at birth, 90% have short great toes (12 Dec 1998) |
| myositis purulenta tropica | A disease observed in Samoa and in tropical Africa, marked by pains in the extremities, fever of a remittent or intermittent type, and abscesses in the muscles in various parts of the body (may result in death from sepsis); causative organisms are Staphylococcus aureus and Streptococcus pyogenes, but usually the disease is associated with parasitic infections. Synonym: bungpagga, lambo lambo, tropical myositis, tropical pyomyositis. (05 Mar 2000) |
| proliferative myositis | A rapidly growing benign infiltrating fibrous nodule in skeletal muscle, containing characteristic giant cells resembling ganglion cells. (05 Mar 2000) |
| inclusion body myositis | <radiology> Common form of inflamatory myopathy, most common in the elderly, equal sex incidence, sporadic idiopathic disease (very rarely familial), misdiagnosed as steroid-resistant polymyositis symptoms, presents as a painless slowly progressive proximal myopathy, may cause dysphagia, mild to moderate muscle wasting diagnosis, serum creatine kinase levels usually normal or only slightly elevated, EMG may show non-specific myopathic features, diagnosis on muscle biopsy, inclusion bodies seen in rimmed vacuoles in skeletal muscle fibres treatment, steroids and immunosuppression generally ineffective, rare patients reported who have made a response to treatment pathogenesis, unknown, ubiquitin, prion protein, tau protein found in inclusions, abnormal mitchondria seen in some case (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|