| 영문 | chronic obstructive pulmonary disease | 한글 | 만성폐쇄폐병 |
|---|---|---|---|
| 설명 | 만성적으로 기도의 폐쇄를 가져오는 병을 이르는 말. 대개 만성기관지염, 기관지 천식, 폐기종의 3가지 병을 말한다. 만성기관지염이란 기관지의 만성염증을 말한다. 기관지의 염증으로 인해서 기관지의 점막에 부종이 생기고 이로 인해서 기관지의 내경이 좁아져서 기도의 폐쇄를 가져온다. 대개 흡연과 밀접한 연관을 가지며, 호흡곤란, 기침, 그리고 가래(대개 색이 푸르고 점도가 높은 가래)가 증상으로 나타난다. 폐기종은 기관지의 벽을 지지하는 조직의 파괴에 의해서 기관지가 제 모양을 갖추지 못하고 무너지게 되어 기도의 폐쇄가 일어나는 병이다. 즉 기관지가 관 모양으로 팽팽하게 펴지는 것을 지지하는 조직의 파괴에 의해서 관모양으로 펴지지 못해 결국은 폐포내에 공기가 차고 폐포벽이 파열되고 기관지가 좁아지게 되는 병을 말한다. 기관지천식이란 여러 가지 자극에 대해서 기관지가 과민한 반응을 보여서 생기는 기관지의 가역적인 폐쇄를 의미한다. 즉 정상인에게서는 기관지의 폐쇄를 보이지 않는 자극에 대해서 기관지의 폐쇄가 생기고 그 자극이 없을 경우에는 기관지의 폐쇄가 없어지는 병을 말한다. |
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| 영문 | pulmonary function tests | 한글 | 폐기능 검사 |
|---|---|---|---|
| 설명 | 여러 가지 기구를 이용해 폐용적 및 허파의 확산능을 알아보는 검사로 말 그대로 허파의 기능을 측정하는 검사이다. |
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| 영문 | pulmonary circulation | 한글 | 폐순환 |
|---|---|---|---|
| 설명 | 전신순환을 거친 산소분압이 낮은 정맥혈이 오른심방으로 들어와 오른심실을 거쳐 폐동맥을 통하여 폐로 가서 가스 교환을 한 후, 산소분압이 높은 동맥혈이 되어 폐정맥을 타고 다시 좌심방으로 돌아오는 혈액의 순환과정을 이르는 말이다. |
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| IPH | idiopathic portal hypertension; idiopathic pulmonary hemosiderosis; idiopathic pulmonary hypertensio... |
|---|---|
| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
| IPS | idiopathic pain syndrome; idiopathic postprandial syndrome; inches per second; infundibular pulmonar... |
| IPF | idiopathic pulmonary fibrosis; infection-potentiating factor; interstitial pulmonary fibrosis |
| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
| IPH | Idiopathic pulmonary haemosiderosis |
|---|---|
| IPF | Idiopathic pulmonary fibrosis |
| AISA | Acquired Idiopathic Sideroblastic Anemia |
| AIS | Adolescent Idiopathic Scoliosis |
| CIU | Chronic Idiopathic Urticaria |
pulmonary pleura
| idiopathic pulmonary haemosiderosis | <chest medicine> A rare, sporadic, fatal, mostly in children with an equal sex distribution. The condition also occurs in adults where there is a sex difference (M:F = 2:1). The patients present with recurrent attacks of pulmonary haemorrhage, acute phase: bat-wing alveolar infiltrates, clears rapidly, chronic findings: haemosiderosis, pulmonary fibrosis, cor pulmonale. (12 Dec 1998) |
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| pulmonary haemosiderosis | Haemosiderosis usually associated with mitral stenosis and marked by an accumulation of macrophages loaded with haemosiderin within the alveoli. (05 Mar 2000) |
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| idiopathic pulmonary fibrosis | <radiology> Aka: usual interstitial pneumonia (UIP), 5-6th decade; M:F = 1:1, clubbing of fingers (83%), lymphocytosis on lavage, increased occurence of bronchogenic CA, average survival of 4-6 years; 87% mortality CXR findings: occasional ground glass pattern in early stage of alveolitis, diffuse reticulations (60%) predominantly at bases, honeycombing, pleural effusion (4%); pleural thickening (6%), pneumothorax in 7% (late stage), progressive volume loss see: interstitial pulmonary fibrosis (12 Dec 1998) |
| idiopathic pulmonary hypertension | <chest medicine> A condition where there is increased blood pressure in the pulmonary arteries with otherwise normal heart and lungs. The cause is unknown, but there is diffuse narrowing of the pulmonary arteries resulting in increased arteriolar pressures. Secondary heart failure ensues without correction of this problem. There is an increased incidence of this disease in females between the ages of 20 and 40 years. Treatment may include a heart and lung transplant in select cases. (27 Sep 1997) |
| haemosiderosis | Conditions in which there is a generalised increase in the iron stores of body tissues, particularly of liver and the reticuloendothelial system, without demonstrable tissue damage. The name refers to the presence of stainable iron in the tissue in the form of haemosiderin. (12 Dec 1998) |
| haemosiderosis / haemochromatosis | <radiology> Iron deposition due to abnormal metabolism or iron overload, primary abnormal iron metabolism, secondary alcoholic cirrhosis, multiple blood transfusions (e.g., Hb SS, thalassaemia) Findings: osteoporosis, chondrocalcinosis (calcium pyrophosphate deposition disease), arthropathy, resembles calcium pyrophosphate deposition disease arthropathy, distinctive feature: BEAK-like osteophytes at MCP jts, mottled increased density of liver and spleen, Definitions: haemosiderosis: haemosiderin deposition within cells, haemochromatosis: haemosiderin within cells AND interstitium (12 Dec 1998) |
| nutritional haemosiderosis | A disease seen in black South Africans that results from ingestion of iron in foodstuffs prepared in iron vessels; excessive absorption of iron affects the liver. (05 Mar 2000) |
| acute idiopathic polyneuritis | <neurology, syndrome> Acute infective polyneuritis that results in a form of peripheral neuropathy with temporary loss of movement and sensation due to inflammation of multiple nerves and loss of myelin. The exact cause is unknown but has been associated with an abnormal immune response to viral infection, particularly cytomegalovirus infection, in which there is cell-mediated immunity to a component of myelin. The disease may be autoimmune in origin and complete recovery can take up to six months. Synonym: Guillain-Barre syndrome (12 Jul 2000) |
| chronic idiopathic jaundice | <syndrome> An inherited disorder (autosomal recessive) that is characterised by long-standing mild jaundice. This occurs secondary to an abnormality in the transport of bilirubin from the liver to the biliary system. This leads to an accumulation of bilirubin in the liver. Avoidance of alcohol and medications which can affect the liver is important. Inheritance: autosomal recessive. (27 Sep 1997) |
| chronic idiopathic xanthomatosis | Vague or indefinite term for inherited abnormalities of lipid metabolism leading to xanthoma formation (e.g., primary familial xanthomatosis). (05 Mar 2000) |
| multiple idiopathic haemorrhagic sarcoma | <oncology, tumour> A type of vascular cancer characterised by soft purple nodules that usually develop first on the feet and then slowly spread across the skin.This cancer is most often found in people with compromised immune systems, such as AIDS patients. (09 Oct 1997) |
| primary idiopathic macular atrophy | Atrophoderma in which the skin becomes bag like and wrinkled. Synonym: atrophia maculosa varioliformis cutis, atrophoderma maculatum, macular atrophy, primary idiopathic macular atrophy, primary macular atrophy of skin. Origin: G. Anetos, relaxed, + derma, skin (05 Mar 2000) |
| purpura, thrombocytopenic, idiopathic | Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IgG autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. (12 Dec 1998) |
| hyperostosis, diffuse idiopathic skeletal | A disease of elderly men characterised by large osteophytes that bridge vertebrae and ossification of ligaments and tendon insertions. (12 Dec 1998) |
| diffuse idiopathic skeletal hyperostosis | A form of degenerative arthritis characteristically associated with flowing calcification along the sides of the vertebrae of the spine and commonly with inflammation (tendinitis) and calcification of the tendons at their attachments points to bone. Because areas of the spine and tendons can become inflamed, antiinflammatory medications (NSAIDs), such ibuprofen, can be helpful in both relieving pain and inflammation. Also called Forestier's disease. (12 Dec 1998) |
| idiopathic | Of the nature of an idiopathy, self originated, of unknown causation. (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|