| 영문 | hookworm | 한글 | 구충 |
|---|---|---|---|
| 설명 | 선충류 원충목 구충과의 기생충을 통틀어 이르는 말. 사람과 그 밖의 포유류에 기생하는 흡혈성 선충이며 구충에는 사람에게 기생하는 아메리카구충(Necator americanus)-십이지장충(Ancylostoma duodenale)과 개-소-양 등에 기생하는 고유의 구충이 있다. 이탈리아의 밀라노에서 처음으로 구충이 발견되었을 때 때마침 십이지장에 기생하고 있었기 때문에 십이지장충이라 명명되었으나, 본래의 기생부위는 오히려 빈창자이고, 현재에는 구충이라 일컬어진다. 입부분에 이빨과 같은 흡착기를 가지고 있으면서 숙주의 장점막에 붙어 피를 빨아먹는 한 무리의 선충들을 가리킨다. 한국에는 개십이지장충(A. caninum)과 소구충(Bunostomum phlebotomus)-양구충(B. trigonocepbalum) 등이 있다. 인체에 기생하는 구충은 몸길이가 대개 1cm 정도이지만 십이지장충은 좀 길고 굵다. 또 십이지장충의 입에는 두 쌍의 이빨이 있고 아메리카 구충은 얇은 널빤지와 같은 모양의 치판이 있다. 대변과 함께 밖으로 나온 알은 적당한 온도-습도-산소가 있으면 부화하여 2회 탈피하여 필라리아형의 감염형 유충이 된다. 십이지장충은 입으로, 아메리카 구충은 피부로 감염된다. 감염된 지 4~7주가 지나면 작은창자 상부에서 성충이 되어 산란을 시작하고 알이 대변으로 나온다. 침입 부위에 가려움-작열감을 일으키고 홍반과 구진, 물집 등을 일으킨다. 십이지장충에 감염되면 채독증을 일으키며 발작성 기침 등의 특이한 증세를 보인다. 또 빈혈이 생기는 수도 있다. 감염을 예방하려면 인분을 위생적으로 처리하고 채소를 깨끗이 씻는 등 위생에 각별히 신경써야 한다. |
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| ACD | Anaemia of chronic disease |
|---|---|
| AIHA | Auto-immune haemolytic anaemia |
| AHA | autoimmune haemolytic anaemia |
| CAV | Chicken Anaemia Virus |
| CAA | Chicken anaemia agent |
| hookworm anaemia | Anaemia associated with heavy infestation by Ancylostoma duodenale or Necator americanus. (05 Mar 2000) |
|---|
| hookworm | A parasitic intestinal infection caused most commonly by Necator americanus or Ancylostoma duodenale. Individuals may be asymptomatic and be carriers. Infection occurs when the larvae invade exposed skin, most commonly the feet. Symptoms can be similar to peptic ulcer disease. (27 Sep 1997) |
|---|---|
| hookworm disease | See: ancylostomiasis, necatoriasis. (05 Mar 2000) |
| hookworm infections | Infection of humans or animals with hookworms other than those caused by the genus ancylostoma or necator, for which the specific terms ancylostomiasis and necatoriasis are available. (12 Dec 1998) |
| achlorhydric anaemia | A form of chronic hypochromic microcytic anaemia associated with achlorhydria or achylia gastrica; observed most frequently in women in the third to fifth decades. Synonym: Faber's anaemia, Faber's syndrome. (05 Mar 2000) |
| achrestic anaemia | A form of chronic progressive macrocytic anaemia that can be fatal in which the changes in bone marrow and circulating blood closely resemble those of pernicious anaemia, but in which there is only transient or no response to therapy with vitamin B12; glossitis, gastrointestinal disturbances, central nervous system disease, and pyrexia are not observed, and there is only little bleeding or haemolysis. Origin: G. A-priv. + chresis, a using (05 Mar 2000) |
| acquired haemolytic anaemia | Nonhereditary acute or chronic anaemia associated with or caused by extracorpuscular factors, e.g., certain infectious agents, chemicals (including autoantibodies or therapeutic agents), burns, toxic materials from higher plant and animal forms (including snake venoms). (05 Mar 2000) |
| addisonian anaemia | <haematology> A form of anaemia (low red blood cell counts) that results when the bone marrow fails to produce adequate numbers of red blood cells due to a deficiency in vitamin B12. Intrinsic factor, necessary for normal B12 absorption, may be the underlying cause for B12 deficiency if is not produced in the gastric glands (in the stomach). Origin: Gr. Haima = blood (27 Sep 1997) |
| Addison's anaemia | <haematology> A form of anaemia (low red blood cell counts) that results when the bone marrow fails to produce adequate numbers of red blood cells due to a deficiency in vitamin B12. Intrinsic factor, necessary for normal B12 absorption, may be the underlying cause for B12 deficiency if is not produced in the gastric glands (in the stomach). Origin: Gr. Haima = blood (27 Sep 1997) |
| anaemia | <haematology> Too few red blood cells in the bloodstream, resulting in insufficient oxygen to tissues and organs. Origin: Gr. Haima = blood (16 Dec 1997) |
| anaemia, aplastic | A form of anaemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. (12 Dec 1998) |
| anaemia, Cooley's | 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. Another name for the disease is Mediterranean anaemia. The name thalassaemia was coined by the Nobel Prise winning pathologist George Whipple and the professor of paediatrics Wm Bradford at Univ. 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) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia gravis | <haematology> This form of anaemia occurs when the bone marrow ceases sufficient red and white blood cell production. It may be induced by exposures to high levels of toxic chemicals, radiation and certain drugs. It is generally unresponsive to specific therapy, often accompanied by granulocytopenia and thrombocytopenia, in which the bone marrow may not necessarily be hypocellular or hypoplastic but fails to produce adequate numbers of peripheral blood elements. The term actually is all inclusive and most probably encompasses several clinical syndromes. Origin: Gr. Haima = blood (29 Sep 1997) |
| anaemia, haemolytic | Anaemia due to decreased life span of erythrocytes. (12 Dec 1998) |
| anaemia, haemolytic, autoimmune | Acquired haemolytic anaemia due to the presence of autoantibodies which agglutinate or lyse the patient's own red cells. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|