| 영문 | bronchiectasis | 한글 | 기관지확장증 |
|---|---|---|---|
| 설명 | 기관지의 내강 일부가 확장되고 변형되는 병. 악취호흡, 기침발작, 점액 및 농성물질의 객출을 특징으로 한다. 기관지를 균등하게 침범하는 경우, 불규칙적으로 주머니 모양으로 발생하는 경우, 기관지 말단이 둥글게 확장하는 경우등이 있다. 확장된 내강이 가래가 고이기 쉽게 되고, 거기에 세균이 감염되어 염증을 일으킨다. 선천적인 원인으로 발생하는 수도 있고 영아 또는 유아 무렵에 폐렴, 백일해, 홍역 따위에 걸린 뒤에 나타나기도 하며, 성인이 흉곽성형술 받은 뒤에 발생하기도 한다. |
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| BEAP | bronchiectasis, eosinophilia, asthma, pneumonia |
|---|---|
| ATN | Acute Tubular Necrosis |
| RTA | Renal Tubular Acidosis |
| Tm | maximum Tubular Transport |
| TRP | Tubular Reabsorption of Phosphate |
| BE | Bronchiectasis |
|---|---|
| ATN | Acute Tubular Necrosis |
| TBM | Anti-tubular basement membrane |
| DRTA | Distal renal tubular acidosis |
| DT | Distal tubular |
| acquired bronchiectasis | <chest medicine> Persistent and progressive dilation of bronchi or bronchioles as a consequence of inflammatory disease (lung infections), obstruction (tumour) or congenital abnormality (for example cystic fibrosis). Symptoms include fetid breath and paroxysmal coughing, with the expectoration of mucopurulent matter. It may affect the bronchioles uniformly (cylindric bronchiectasis) or occur in irregular pockets (sacculated bronchiectasis) or the dilated bronchi may have terminal bulbous enlargements (fusiform bronchiectasis). Although rarely congenital, it is most often an acquired condition in childhood. (13 Nov 1997) |
|---|---|
| bronchiectasis | <chest medicine> Persistent and progressive dilation of bronchi or bronchioles as a consequence of inflammatory disease (lung infections), obstruction (tumour) or congenital abnormality (for example cystic fibrosis). Symptoms include fetid breath and paroxysmal coughing, with the expectoration of mucopurulent matter. It may affect the bronchioles uniformly (cylindric bronchiectasis) or occur in irregular pockets (sacculated bronchiectasis) or the dilated bronchi may have terminal bulbous enlargements (fusiform bronchiectasis). Although rarely congenital, it is most often an acquired condition in childhood. (13 Nov 1997) |
| congenital bronchiectasis | Persistent and progressive dilation of bronchi or bronchioles as a consequence of inflammatory disease (lung infections), obstruction (tumour) or congenital abnormality (for example cystic fibrosis). Although rarely congenital, it is most often an acquired condition in childhood. (27 Sep 1997) |
| cylindrical bronchiectasis | Bronchiectasis resulting in dilated bronchi of cylindrical shape; i.e., of uniform caliber. (05 Mar 2000) |
| cystic bronchiectasis | Bronchiectasis in which the bronchi end in blind sacs greater in diameter than the draining bronchi. See: saccular bronchiectasis. (05 Mar 2000) |
| saccular bronchiectasis | Bronchiectasis resulting in dilated bronchi of saccular or irregular shape. See: cystic bronchiectasis. (05 Mar 2000) |
| dry bronchiectasis | Bronchiectasis characterised by lack of productive cough and by occasional haemoptysis. Synonym: bronchiectasia sicca. (05 Mar 2000) |
| acute tubular necrosis | <nephrology> A kidney disorder that results in damage to the renal tubule cells leading to acute renal failure. Acute tubular necrosis can result from any condition which deprives the kidney of oxygen (ischaemia). Acute tubular necrosis may occur as a complication of shock, trauma or sepsis. Conditions such as diabetes or liver disease can predispose people to the development of acute tubular necrosis. Certain medications (for example aminoglycosides, amphotericin B, cyclosporine) are known to cause acute tubular necrosis as a toxic side effect. Radiopaque contrast dyes, used in some radiologic procedures, may also result in acute tubular necrosis as a rare complication from contrast dye use. Acronym: ATN (13 Nov 1997) |
| renal tubular acidosis | <nephrology> A rare sometimes familial disorder of the renal tubule characterised by the inability to excrete urine of normal acidity. This leads to a hyperchloraemic acidosis which is often associated with one or more secondary complications such as hypercalcinuria with nephrolithiasis and nephrocalcinosis, rickets, or osteomalacia and severe potassium depletion. (25 Jun 1999) |
| renal tubular transport, inborn errors | Genetically determined disorders of the reabsorptive functions of the kidney with regard to specific nephron segments responsible for specific transport functions, classifiable by proximal nephron function, loop of henle function, and distal nephron function. The transport defects can be selective or nonselective. (12 Dec 1998) |
| Pick's tubular adenoma | A neoplasm of the ovary, arising from the ovarian stroma, mimicking to a greater or lesser extent derivatives of the sex cord mesenchyme of the testis, and sometimes causing defeminization and virilization. (12 Dec 1998) |
| primary renal tubular acidosis | A metabolic defect in the mechanism of urinary acidification that may be either the transient type, with onset in infancy, or the persistent type, with onset in childhood or adult years; both types are familial. (05 Mar 2000) |
| secondary renal tubular acidosis | Renal tubular acidosis that may occur as a complication of hypercalcaemic states, hyperglobulinaemic disorders, and in some other chronic renal conditions; a regular component of De Toni-Fanconi syndrome. (05 Mar 2000) |
| osteopetrosis with renal tubular acidosis | <syndrome> An inherited deficiency of carbonic anhydrase II that results in osteopetrosis and metabolic acidosis. Synonym: osteopetrosis with renal tubular acidosis. (05 Mar 2000) |
| ovarian tubular adenoma | <oncology, tumour> A type of ovarian tumour whose sells secrete a male sex hormone (testosterone) causing virilisation in women. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|