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| ¿µ¹® | planes of body | ÇÑ±Û | ÀÎüÀÇ ¸é |
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| ¼³¸í | ÀÎü¸¦ ¿©·¯ °³·Î ³ª´©´Â ¸éÀÌ Àִµ¥, Å©°Ô ½Ã»ó¸é(sagittal plane), °ü»ó¸é(coronal plane), ¼öÆò¸é(horizontal plane)À¸·Î ³ª´ ¼ö ÀÖ´Ù. ½Ã»ó¸éÀº ÀÎü¸¦ Á¿ì·Î, °ü»ó¸éÀº ¾ÕµÚ·Î, ¼öÆò¸éÀº À§¾Æ·¡·Î °¡¸£´Â ¸éÀÌ´Ù. |
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| IB | idiopathic blepharospasm; immune body; inclusion body; index of body build; infectious bronchitis; I... |
|---|---|
| AIE | acute inclusion-body encephalitis; acute infectious encephalitis; acute infective endocarditis |
| CIBHA | congenital inclusion-body hemolytic anemia |
| IBM | inclusion body myositis |
| IncB | inclusion body |
| IBH | Inclusion Body Hepatitis |
|---|---|
| IBM | Inclusion body myositis |
| LBHI | Lewy body-like hyaline inclusion |
| S-IBM | Sporadic inclusion body myositis |
| AEP | Acute eosinophilic pneumonia |
| acute inclusion body encephalitis | The most common acute encephalitis, caused by HSV-1; affects persons of any age; preferentially involves the inferomedial portions of the temporal lobe and the orbital portions of the frontal lobes; pathologically, severe haemorrhagic necrosis is present along with, in the acute stages, intranuclear eosinophilic inclusion bodies in the neurons and glial cells. Synonym: acute inclusion body encephalitis, herpes encephalitis. (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) |
| subacute inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| inclusion body disease | <disease> An illness in newborns caused by viral infection, symptoms includefever, cellular enlargement, microscopically-visible clumps of viralparticles or proteins in the cytoplasm and nuclei of affected cells, enlargementof the spleen and liver. Long-term effects of the disease may includemental retardation. (09 Oct 1997) |
| inclusion body encephalitis | <neurology> Chronic progressive illness seen in children a few years after measles infection and involving demyelination of the cerebral cortex. Virus apparently persists in brain cells: usually considered a slow virus disease. (18 Nov 1997) |
| 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) |
| inclusion body rhinitis | A respiratory disease of pigs caused by the cytomegalovirus porcine herpesvirus 2 and characterised by rhinitis and conjunctivitis in young pigs. (05 Mar 2000) |
| parasitic eosinophilic lung disease | <radiology> All are metazoans (mostly nematodes), Ascaris, Strongyloides, Ancyclostoma, Schistosoma, tropical pulmonary eosinophilia, pulmonary larva migrans (12 Dec 1998) |
| chronic eosinophilic pneumonia | <radiology> Idiopathic, associated with allergies and desensitization, variant of Loeffler pneumonia, treatment: corticosteroids Findings: reverse pulmonary oedema pattern (= Loeffler's), areas of consolidation persists (days to weeks) see: eosinophilic lung disease (12 Dec 1998) |
| drug-induced eosinophilic lung disease | <radiology> Diffuse reticular pattern: nitrofurantoin, Loeffler-like pattern: penicillin, sulfonamides, ASA, para-ASA, imipramine, HCTZ, cromolyn sodium see: eosinophilic lung disease (12 Dec 1998) |
| eosinophilic | Staining readily with eosin dyes; denoting such cell or tissue elements. (05 Mar 2000) |
| eosinophilic cellulitis | <syndrome> Recurrent cellulitis followed by brawny edematous skin lesions, or a less acute presentation of papular, annular, or gyrate skin lesions which are sometimes urticarial; affected skin and subcutis are heavily infiltrated by eosinophils and histiocytes, with scattered small necrotic foci (flame figures) of varied aetiology; sometimes follows an arthropod bite. Synonym: eosinophilic cellulitis. (05 Mar 2000) |
| eosinophilic cystitis | Bladder inflammation with many eosinophils in urinary sediment as well as bladder wall. (05 Mar 2000) |
| eosinophilic endomyocardial disease | A restrictive cardiomyopathy associated with hyperproduction of eosinophiles and their cardiac infiltration, clinically characterised by diastolic and later systolic ventricular failure. (05 Mar 2000) |
| eosinophilic fasciitis | <pathology> A syndrome which is characterised by inflammation of the fascia and muscles of the extremities. Infiltrations of eosinophils are found in affected muscle tissue and fascia. The cause is unknown. Symptoms include tenderness and swelling of arms and legs, joint contractures, bone apins, muscle aches and muscle weakness. Some may complain of carpal tunnel syndrome symptoms with numbness and tingling in the hands. Diagnosis is made by tissue biopsy. Treatment includes systemic corticosteroids. The illness can last for 3 to 5 years and then ususally resolves. (27 Sep 1997) |
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