| 영문 | chronic lymphocytic leukemia | 한글 | 만성림프성 백혈병 |
|---|---|---|---|
| 설명 | 백혈병(leukemia)란 비정상적인 백혈구 세포의 증식에 의해 일어나는 병적인 상태를 말하는데, 흔히 말초혈액에 미분화세포가 나타나며, 정상적인 적혈구세포와 백혈구세포, 혈소판의 급격한 감소를 가져와 정상적인 세포에 의해 행해지는 여러 기능의 감소를 주증상으로 하여 병원에 찾아오게 된다. 따라서 적혈구세포의 감소로 인한 빈혈, 백혈구세포의 감소로 인한 많은 감염증세(흔히 걸리지 않는 세균에 의한 감염, 지나치게 잦은 감기, 폐렴 등), 혈소판세포의 감소로 인한 출혈증상이 나타난다. 또한 피를 생산하는 골수 조직에서는 이런 비정상적인 세포의 증식만을 볼 수 있으며, 정상적인 세포의 증식은 보기 힘들다. 만성림프성 백혈병은 서양에서는 비교적 백혈병 중에서 흔한 형이지만 동양권에서는 아주 드문 백혈병의 형태이다. 대개 60세 이상의 고령층에서 많이 생기고 30세 이하에서는 거의 찾아볼 수가 없다. 혈액검사상에서 림프구의 많은 증가를 볼 수가 있고, 대신에 다른 혈액세포들은 감소를 나타낸다. 백혈병 중 예후가 좋은 편이며 대개 치료는 항암제를 이용한 화학요법을 많이 사용하며, 평균 생존기간은 4~5년이다. |
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| 영문 | interstitial therapy | 한글 | 근접치료 |
|---|---|---|---|
| 설명 | 주로 종양의 치료를 목적으로 하여 인체 조직내에 방사선 물질을 삽입하여 방사선을 조사하는 치료법이다. Brachytherapy라고도 한다. |
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| 영문 | nephritis(interstitial) | 한글 | 콩팥염, 신장염(간질성) |
|---|---|---|---|
| 설명 | 콩팥사이질(renal interstitium: 콩팥의 세뇨관 사이의 결합조직)의 염증. 급성으로 일어나는 간질콩팥염은 대개 많은 약을 복용한 후에 발생하는 데, 열, 피부의 변색, 혈액내의 호산구증 그리고 소변의 감소와 콩팥기능의 감소를 특징으로 한다. 치료는 복용중인 약을 끊고, 부신겉질호르몬제를 투여한다. 콩팥은 각종 노폐물, 전해질, 수분 등을 포함한 요를 생산하여 배출하는 동시에 수소이온, 나트륨, 칼륨, 인산 이온 농도 등을 조절하며 내분비와 외분비 기능에 관여하기도 한다. |
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| ILP | inadequate luteal phase; insufficiency of luteal phase; interstitial laser photocoagulation; interst... |
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| NIP | Non-specific Interstitial Pneumonitis |
| CIPF | classic interstitial pneumonitis-fibrosis; clinical illness promoting factor |
| DIFP | diffuse interstitial fibrosing pneumonitis; diisopropyl fluorophosphonate |
| DIP | desquamative interstitial pneumonitis; diisopropyl phosphate; diisopropylamine; diphtheria; distal i... |
| LIP | Lymphocytic Interstitial Pneumonitis |
|---|---|
| IP | Interstitial Pneumonitis |
| LIP | Lymphoid interstitial pneumonitis |
| LIP | Lymphocytic interstitial pneumonia |
| EHP | Experimental hypersensitivity pneumonitis |
| lymphocytic interstitial pneumonitis | A rare disease characterised by interstitial accumulation of lymphocytes in the lungs and late fibrosis; usually a result of a lymphoma, occasionally seen in AIDS, especially. In children. Sometimes seen as an autoimmune disorder. Synonym: lymphocytic interstitial pneumonia, lymphoid interstitial pneumonia. (05 Mar 2000) |
|---|---|
| acute interstitial pneumonitis | Usually considered a form of hypersensitivity pneumonitis. (05 Mar 2000) |
| interstitial pneumonitis | <chest medicine, pathology> A form if pneumonia which involves the interstitial tissues (connective tissue) of the lung. Causes are varied and include: infection with Pneumocystis carinii, radiation exposure, toxic inhalation, viral pneumonias and giant cell pneumonia. (27 Sep 1997) |
| lymphoid interstitial pneumonitis | <pathology> A form of pneumonia which is characterised by diffuse interstitial infiltrates and infiltration of lymphocytes into the lung tissue. (27 Sep 1997) |
| lymphocytic interstitial pneumonia | A rare disease characterised by interstitial accumulation of lymphocytes in the lungs and late fibrosis; usually a result of a lymphoma, occasionally seen in AIDS, especially. In children. Sometimes seen as an autoimmune disorder. Synonym: lymphocytic interstitial pneumonia, lymphoid interstitial pneumonia. (05 Mar 2000) |
| acute chemical pneumonitis | <chest medicine> Inflammation of the lungs which occurs secondary to exposure to a chemical, organic dust, fungus or mould. Chronic exposure can lead to chronic lung changes evident on chest X-ray. Symptoms include cough, fever, shortness of breath and wheezing. See: bird-handler's disease. (27 Sep 1997) |
| radiation pneumonitis | Injurious effects of radiotherapy on the lungs. There are three phases in the reaction of the lungs to radiation injury: an acute phase occurring 1 to 2 months after exposure, a subacute phase 2 to 9 months after exposure, and a chronic or fibrotic phase more than 9 months after exposure. In the acute phase there is vascular damage, congestion, oedema, and mononuclear cell infiltration; in the subacute phase the alveolar walls are infiltrated with mononuclear inflammatory cells and fibroblasts; in the chronic phase, alveolar fibrosis and capillary sclerosis take place. (cecil textbook of medicine, 19th ed, p2343) (12 Dec 1998) |
| pandora's pneumonitis | <radiology> Type of extrinsic allergic alveolitis, from forced air equipment (heating, humidifying, air conditioning systems), organism: thermophilic actinomycetes (12 Dec 1998) |
| pneumonitis | <pathology> Inflammation of the lung secondary to viral or bacterial infection. Common symptoms include a productive cough, fever, chills and shortness of breath. (27 Sep 1997) |
| hypersensitivity pneumonitis | <radiology> Aka: chronic extrinsic allergic alveolitis, pathology: proliferation of epithelial cells, elaboration of reticulum fibres, findings: interstitial reticulonodular pattern (basilar distribution), volume loss (cicatrization atelectasis) in upper lobes, pleural effusion (rare), lymph node enlargement may occur (12 Dec 1998) |
| feline pneumonitis | An infectious respiratory illness of domesticated cats caused by the bacterium Chlamydia psittaci. (05 Mar 2000) |
| uraemic pneumonitis | Perihilar oedema of the lung associated with renal failure and hypertension; the peripheral parts of the lung remain clear. Synonym: uraemic pneumonia, uraemic pneumonitis. (05 Mar 2000) |
| acute lymphocytic leukaemia | <radiology> 95% of cases of leukaemia in children, bone changes in 50-70% of kids (vs. 10% in adults); seen as early as 1 month after onset of symptoms, wrists and knees most commonly affected, bony defects: metaphyseal radiolucent bands! (similar findings in scurvy, JRA, syphilis), osteolytic lesions, periosteal reaction, osteosclerosis (12 Dec 1998) |
| acute non-lymphocytic leukaemia | <haematology> A form of leukaemia which is characterised by the proliferation of immature bone marrow precursor cells in the marrow and immature white blood cells (granulocytes) in the bloodstream. Occurs primarily in adults and in infants under 1 year of age. Complications include abnormal bleeding and susceptibility to infections. Symptoms include fatigue, weight loss, fevers, weakness, pallor, bone pains, bleeding gums, nosebleeds, easy bruising, enlarged lymph nodes and joint pains. Trisomy-8 is the most common cytogenetic abnormality observed, followed by monosomy-7 and monosomy-5. Approximately 8% of cases show trisomy-8, mostly in AML (M1), AM (M4) and acute monocytic leukaemia (M5). Many pre-leukaemic conditions, acute non-lymphocytic leukaemia and secondary leukemia show monosomy-7 or deletion of the long arm of chromosome 7. Treatment includes chemotherapy and/or bone marrow transplant. Acronym: ANLL Incidence: 2.5 cases per 100,000 (all ages). Origin: Gr. Haima = blood (07 Apr 1998) |
| chronic lymphocytic leukaemia | <haematology> A slowly progressing form of leukaemia, characterised by an increased number of the type of white blood cell known as lymphocytes. With about 3, 500 new cases occurring each year in the UK, it is the most common form of leukaemia and occurs predominantly in late middle age onwards. It has variable symptoms and course, but may be diagnosed by chance before the patient develops any clinical symptoms of disease. Acronym: CLL Origin: Gr. Haima = blood (12 Jan 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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