| 영문 | lymphoma | 한글 | 림프종 |
|---|---|---|---|
| 설명 | 림프절에 생긴 악성 종양. 이 암은 백혈병과는 다르다. 림프성 백혈병은 골수에서 생긴 림프구성 악성종양이지만, 림프종은 림프절에서 생긴 림프구성 악성종양이다. 림프종은 크게 2가지 즉 호지킨림프종(Hodgkin's lymphoma)과 비호지킨림프종(Non-Hodgkin's lymphoma)으로 나눌수 있다. 또한 비호즈킨림프종은 여러 가지의 세포형태에 따라 나누고 있다. 이 병은 단지 림프절뿐만 아니라 지라, 골수, 이외 다른 기관을 침범함으로써 악성이며, 생명에 큰 위협을 준다. 특이한 형태로 버킷림프종(Burkitt's lymphoma)가 있다. 이 병은 주로 어린이에게 일어나며 주로 중앙 아프리카에 많이 발생한다. 또한 이 병은 바이러스(Ebstein Barr virus)에 의해서 일어나는 것으로 알려져 있다. 주된 침범부위는 얼굴의 아래턱뼈이다. |
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| 영문 | non-Hodgkin lymphoma | 한글 | 비호지킨 림프종 |
|---|---|---|---|
| 설명 | 림프종은 림프절에 생긴 악성 종양으로 백혈병과는 다르다. 백혈병은 골수에서 생긴 림프구성 악성종양이지만, 림프종은 림프조직에서 생긴 림프구성 악성종양이다. 크게 림프종은 2가지로 나눌 수 있는 데, 호지킨병(Hodgkin's lymphoma)과 비호지킨림프종(non-Hodgkin's lymphoma)으로 나눌 수 있다. 또한 비호지킨림프종은 여러 가지의 세포형태에 따라 나누고 있다. 이 병은 단지 림프절뿐만 아니라 지라, 골수, 이외 다른 기관을 침범함으로써 악성이며, 생명에 큰 위협을 준다. 악성림프종의 일종. 전이의 형태가 다양하여, 주위 림프절을 건너뛰어 다른 림프절로 전이하기도 한다. 또한 세포의 형태에 따라 여러 가지 종류가 있으며 대개 치료는 방사선치료와 화학요법을 복합하여 사용한다. |
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| FMF | familial Mediterranean fever; fetal movement felt; flow microfluorometry; forced midexpiratory flow |
|---|---|
| MSF | macrophage slowing factor; macrophage spreading factor; Medicins sans Frontieres [Doctors without Bo... |
| HL | hairline; hairy leukoplakia; half life; hearing level; hearing loss; heparin lock; histiocytic lymph... |
| NHL | nodular histiocytic lymphoma; non-Hodgkin lymphoma |
| ATL | Adult T cell Lymphoma |
| EMR | Eastern Mediterranean Region |
|---|---|
| FMF | Familial Mediterranean Fever |
| MSF | Mediterranean Spotted Fever |
| ARL | AIDS)-related lymphoma |
| ATL | Adult T cell leukaemia-lymphoma |
| Mediterranean lymphoma | A spectrum of conditions ranging from a benign plasma cell hyperplasia to a highly malignant lymphoma of the small intestine. (12 Dec 1998) |
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| anaemia, mediterranean | Better known today as thalassaemia (or as beta thalassaemia or thalassaemia major).The clinical picture of this important type of anaemia was first described in 1925 by the paediatrician Thomas Benton Cooley. The name thalassaemia was coined by the Nobel Prise winning pathologist George Whipple and the professor of paediatrics Wm Bradford at U. Of Rochester because thalassa in Greek means the sea (like the Mediterrranean Sea) + -aemia means in the blood so thalassaemia means sea in the blood. Thalassaemia is not just one disease. It is a complex contingent of genetic (inherited) disorders all of which involve underproduction of haemoglobin, the indispensable molecule in red blood cells that carries oxygen. The globin part of normal adult haemoglobin is made up of 2 alpha and 2 beta polypeptide chains. In beta thalassaemia, there is a mutation (change) in both beta globin chains leading to underproduction (or absence) of beta chains, underproduction of haemoglobin, and profound anaemia. The gene for beta thalassaemia is relatively frequent in people of Mediterranean origin (for example, from Italy and Greece). Children with this disease inherit one gene for it from each parent. The parents are carriers (heterozygotes) with just one thalassaemia gene, are said to have thalassaemia minor, and are essentially normal. Their children affected with beta thalassaemia seem entirely normal at birth because at birth we still have predominantly foetal haemoglobin which does not contain beta chains. The anaemia surfaces in the first few months after birth and becomes progressively more severe leading to pallor and easy fatiguability, failure to thrive (grow), bouts of fever (due to infections) and diarrhoea. Treatment based on blood transfusions is helpful but not curative. Gene therapy will, it is hoped, be applicable to this disease. (12 Dec 1998) |
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| mediterranean anaemia | Better known today as thalassaemia (or as beta thalassaemia or thalassaemia major).the clinical picture of this important type of anaemia was first described in 1925 by the paediatrician thomas benton cooley. The name thalassaemia was coined by the nobel prise winning pathologist george whipple and the professor of paediatrics wm bradford at u. Of rochester because thalassa in greek means the sea (like the mediterrranean sea) + -aemia means in the blood so thalassaemia means sea in the blood. Thalassaemia is not just one disease. It is a complex contingent of genetic (inherited) disorders all of which involve underproduction of haemoglobin, the indispensable molecule in red blood cells that carries oxygen. The globin part of normal adult haemoglobin is made up of 2 alpha and 2 beta polypeptide chains. In beta thalassaemia, there is a mutation (change) in both beta globin chains leading to underproduction (or absence) of beta chains, underproduction of haemoglobin, and profound anaemia. The gene for beta thalassaemia is relatively frequent in people of mediterranean origin (for example, from italy and greece). Children with this disease inherit one gene for it from each parent. The parents are carriers (heterozygotes) with just one thalassaemia gene, are said to have thalassaemia minor, and are essentially normal. Their children affected with beta thalassaemia seem entirely normal at birth because at birth we still have predominantly foetal haemoglobin which does not contain beta chains. The anaemia surfaces in the first few months after birth and becomes progressively more severe leading to pallor and easy fatiguability, failure to thrive (grow), bouts of fever (due to infections) and diarrhoea. Treatment based on blood transfusions is helpful but not curative. Gene therapy will, it is hoped, be applicable to this disease. (12 Dec 1998) |
| Mediterranean exanthematous fever | An affection occurring sporadically in the Mediterranean littoral marked by a severe chill with abrupt rise of temperature, pains in the joints, tonsillitis, diarrhoea, vomiting, and, on the third to fifth day, a rash of elevated nonconfluent macules beginning on the thighs and spreading to the entire body; lasts from ten days to two weeks and then disappears by rapid lysis without desquamation; probably caused by Rickettsia conorii, like Boutonneuse fever. (05 Mar 2000) |
| mediterranean fever | See Familial Mediterranean Fever. (12 Dec 1998) |
| mediterranean islands | Scattered islands in the mediterranean sea. The chief islands are the balearic islands (belong to spain; majorca and minorca are among these), corsica (belongs to france), crete (belongs to greece), cyprus (a republic), the cyclades, dodecanese and ionian islands (belong to greece), malta (a republic), sardinia and sicily (belong to italy). (12 Dec 1998) |
| mediterranean region | The mediterranean sea, the mediterranean islands, and the countries bordering on the sea collectively. (12 Dec 1998) |
| Mediterranean theileriosis | tropical theileriosis |
| familial mediterranean fever | An inherited intestinal disorder that is characterised by recurrent fevers and intestinal inflammation. Usually has onset between the ages of 5 and 15 years and is more common in those of Mediterranean descent. Symptoms include fevers and abdominal pain. Some may also suffer from chest pains, multiple joint pains and red swollen legs. (27 Sep 1997) |
| fever, mediterranean | See Familial Mediterranean Fever. (12 Dec 1998) |
| adult T-cell lymphoma | <tumour> An acute or subacute disease associated with a human T-cell virus, with lymphadenopathy, hepatosplenomegaly, skin lesions, peripheral blood involvement, and hypercalcaemia. Synonym: adult T-cell leukaemia. (05 Mar 2000) |
| anaplastic large cell lymphoma | <tumour> A form of lymphoma characterised by anaplasia of cells, sinusoidal growth, and immunoreactivity with CD30 (Ki-1 or Ber-H2). Synonym: Ki-1+ lymphoma. (05 Mar 2000) |
| benign lymphoma of the rectum | A rectal polyp composed of lymphoid tissue with follicle formation, covered by mucosa. (05 Mar 2000) |
| burkitt lymphoma | A form of undifferentiated malignant lymphoma usually found in central africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumour in virtually all cases of burkitt lymphoma. The epstein-barr virus (herpes virus 4, human) has been isolated from burkitt lymphoma cases in africa and it is implicated as the causative agent in these cases; however, most non-african cases are ebv-negative. (12 Dec 1998) |
| Burkitt's lymphoma | <oncology, tumour> A type of Non-Hodgkin lymphoma that most often occurs in young people between the ages of 12 and 30. The disease usually causes a rapidly growing tumour in the abdomen. (12 May 1997) |
| cancer, lymphoma, hodgkin's | A type of lymphoma (cancer of the lymphatic system). The most common symptom of Hodgkin's disease is a painless swelling in the lymph nodes in the neck, underarm, or groin. Hodgkin's disease is diagnosed when abnormal tissue is detected by a pathologist after a biopsy of an enlarged lymph node. Treatment usually includes radiation therapy or chemotherapy. Regular follow-up examinations are important after treatment for Hodgkin's disease. Patients treated for Hodgkin's disease have an increased risk of developing other types of cancer later in life, especially leukaemia. (12 Dec 1998) |
| Mediterranean lymphoma |
A diffuse type of small intestine lymphoma, associated with Alfa Chain Disease and mostly occuring in the Mediterranean area and Near East. The patienns ar often young, around or below 20 years of age.
출처: www.gastrolab.net/dictem.htm
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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