| 영문 | secondary infection | 한글 | 이차감염 |
|---|---|---|---|
| 설명 | 어떤 병원체의 감염에 의하여 본인의 저항력이 약해졌을 때 몸의 다른 부위로 전이하여 다시 감염을 일으키는 것. 병원체가 인체에 침입하여 특정한 기관이나 조직에서 병원체가 증식하고, 그곳에 특유의 병터를 일으키는 것이 1차감염 또는 초감염이다. 이 1차감염의 병터의 병원체가 혈관-림프관-기관-소화관-요관 등의 길을 따라 같은 기관의 다른 부위나 다른 기관으로 운반되어 감염을 일으킨다. 따라서 1차감염에 의하여 충분한 면역이 될 경우에는 2차감염이 일어나지 않는다. 예를 들어, 유행성 감기에 걸렸을 때 세균에 의한 폐렴이 뒤따르는 경우를 이른다. 폐렴균, 화농알균, 대장균 따위가 있다. |
||
| 영문 | magnetic resonance imaging(MRI) | 한글 | 자기공명영상 |
|---|---|---|---|
| 설명 | 인체의 장기나, 병적인 모양, 종양의 위치, 림프절의 비대 등에 대한 진단을 내리기 위해 시행하는 방사선학적인 검사방법이다. 현재 많이 쓰이고 있는 컴퓨터단층촬영술(CT: computerized tomography)과는 다른 방법으로 시행하며, 그 해상도가 컴퓨터단층촬영보다는 뛰어나 비록 고가이긴 하지만, 많이 쓰이고 있다. 또한 인체에 무해하고, 여러 가지 면에서 사람을 단층으로 분리시켜 볼 수 있는 등 장점이 많다. 단점은 심장박동기를 설치한 사람이나, 주위에 장을 띠는 물체를 몸에 지니고 있는 중환자 등에서는 이용할 수 없고, 복부장기에 대한 진단에는 컴퓨터단층촬영보다 불리한 것으로 되어 있으며, 무엇보다 설치비와 그 시술비가 비싸다는데 가장 큰 단점이 있다. |
||
| 영문 | electron microscope | 한글 | 전자현미경 |
|---|---|---|---|
| 설명 | 전기 마당 또는 자기 마당을 이용하여 전자류를 전자 렌즈에 집속시켜, 그 통로에 놓인 표본의 상을 확대하는 장치. 광학 현미경보다 훨씬 뛰어난 분해 능력을 가진다. |
||
| SA | salicylic acid; saline [solution]; salt added; sarcoidosis; sarcoma; scalenus anticus; secondary ame... |
|---|---|
| EM | early memory; ejection murmur; electromagnetic; electron micrograph; electron microscopy, electron m... |
| SEM | sample evaluation method; scanning electron microscopy; secondary enrichment medium; standard error ... |
| DTI | dipyridamole-thallium imaging; Doppler tissue imaging |
| EPI | echo planar imaging; electronic portal imaging; Emotion Profile Index; epilepsy; epinephrine; epithe... |
| SE | secondary electron |
|---|---|
| BEI | Backscattered Electron Imaging |
| ESI | Electron Spectroscopic Imaging |
| EPRI | Electron paramagnetic resonance imaging |
| LSIMS | Liquid secondary ion mass spectrometry |
| secondary electron imaging | <microscopy> Production of secondary electrons is very topography related. Due to their low energy, 5eV, only secondaries that are very near the surface (less than 10nm) can exit the sample and be examined. Any changes in topography in the sample that are larger than this sampling depth will change the yield of secondaries due to collection efficiencies. Collection of these electrons is aided by using a collector in conjunction with the secondary electron detector. The collector is a grid or mesh with a +100V potential applied to it which is placed in front of the detector, attracting the negatively charged secondary electrons to it which then pass through the grid-holes and into the detector to be counted. When a Secondary Electrons collide with the solid-state saemiconductor detector an electron-hole pairs are created which are then counted. This quantity is translated into a pixel intensity and displayed on the CRT, forming the image. (05 Aug 1998) |
|---|
| backscattered electron imaging | <microscopy> The production of backscattered electrons from a sample varies directly with the specimen's average atomic number, higher atomic number elements produce more backscattered electrons than lower atomic number ones. Detection of Backscattered Electrons is achieved by using a donut shaped solid state saemiconductor device mounted on the bottom of the objective lens. When Backscattered Electrons strike the detector electron-hole pairs are created which are then counted. This quantity is translated into a pixel intensity and displayed on the CRT, forming the image. By splitting the detector into halves (or quadrants) differences in the signal level on the individual detector segments provide surface topography information. (05 Aug 1998) |
|---|---|
| secondary electron | <microscopy> Produced by an incident electron passing near an atom in the specimen, near enough to impart some of its energy to a lower energy electron (usually in the K-shell). This causes a slight energy loss and path change in the incident electron and the ionisation of the electron in the specimen atom. This ionised electron then leaves the atom with a very small kinetic energy (5eV) and is then termed a secondary electron. Each incident electron can produce several secondary electrons. (05 Aug 1998) |
| adrenal imaging | <radiology> Cortex, I-131 iodo-cholesterol, not widely used due to high rad dose and 4-15 day delayed imaging, medulla, search for pheo, MIBG (I-131 meta-iodobenzylguanidine) (12 Dec 1998) |
| adrenal medullary imaging | <investigation, radiology> A nuclear scan that images the adrenal glands after a radioactive tracer is injected into the bloodstream. This test is useful in detecting a pheochromocytoma, particularly if it not within the adrenal gland. (27 Sep 1997) |
| blood pool imaging | Nuclear medicine study using a radionuclide that is confined to the vascular compartment. (05 Mar 2000) |
| bone: gallium imaging | <radiology> Increased activity in: active osteomyelitis (90% sensitivity: better than Tc-99m MDP), sarcoma, cellulitis, septic arthritis, rheumatoid arthritis, Paget disease, metastases (65% sensitivity: than for bone agents) see: gallium: indications (12 Dec 1998) |
| bright field imaging | <microscopy> An imaging mode in a transmission electron microscopy that uses only unscattered Electrons to form the image. Contrast in such an image is due entirely to mass-thickness variations in amorphous samples, and may include diffraction contrast in crystalline samples. (05 Aug 1998) |
| cardiac blood pool imaging | This noninvasive test uses radioactive tracers to delineate the hearts chambers and major vessels. It may be used to detect a heart attack, heart muscle function and coronary artery disease. The patient receives a radioactive tracer by injection (into a vein) and then the heart is imaged using a gamma camera. The heart is imaged before and after exercise. This test may be used to detect and evaluate atrial septal defect, dilated cardiomyopathy, congestive heart failure, cardiomyopathy, Lyme disease (secondary), mitral stenosis and superior vena cava syndrome. (27 Sep 1997) |
| radionuclide imaging | Process whereby a radionuclide is injected or measured (through tissue) from an external source, and a display is obtained from any one of several rectilinear scanner or gamma camera systems. The image obtained from a moving detector is called a scan, while the image obtained from a stationary camera device is called a scintiphotograph. (12 Dec 1998) |
| Magnetic Resonance Imaging | A special imaging technique used to image internal stuctures of the body, particularly the soft tissues. An MRI image is often superior to a normal X-ray image. It uses the influence of a large magnet to polarize hydrogen atoms in the tissues and then monitors the summation of the spinning energies within living cells. Images are very clear and are particularly good for soft tissue, brain and spinal cord, joints and abdomen. These scans may be used for detecting some cancers or for following their progress. Acronym: MRI (11 Nov 1997) |
| magnetic resonance imaging, cine | A type of imaging technique used primarily in the field of cardiology. By coordinating the fast gradient-echo mri sequence with retrospective ecg-gating, numerous short time frames evenly spaced in the cardiac cycle are produced. These images are laced together in a cinematic display so that wall motion of the ventricles, valve motion, and blood flow patterns in the heart and great vessels can be visualised. (12 Dec 1998) |
| malignant melanoma: gallium imaging | <radiology> Greater than50% sensitivity for primary and metastatic sites: 73% sensitivity if lesion is greater than 2 cm, 17% sensitivity if less than 2 cm, see: gallium: indications malignant melanoma (12 Dec 1998) |
| gated blood pool imaging | Radionuclide ventriculography where scintigraphic data is acquired during repeated cardiac cycles at specific times in the cycle, using an electrocardiographic synchroniser or gating device. Analysis of right ventricular function is difficult with this technique; that is best evaluated by first-pass ventriculography (ventriculography, first-pass). (12 Dec 1998) |
| ratio imaging fluorescence microscopy | <procedure> A method of measurement of intracellular pH or intracellular calcium levels, using a fluorescent probe molecule (see fura-2), in which the two different excitation wavelengths are used and the emitted light levels compared. If emission at one wavelength is sensitive to the intracellular ion level and emission at the other wavelength is not, then standardisation for intracellular probe concentration, efficiency of light collection, inactivation of probe and thickness of cytoplasm can all be performed automatically. (17 Dec 1997) |
| ventilation/perfusion lung imaging | <radiology> See: ventilation agents, perfusion agents, Biello-Siegel criteria (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|