| ECG | Electro-Cardio-Graphy(-Gram); 심전도 = EKG 1. Conducting System Structu... |
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| PMD | Progressive Muscular Dystrophy; 진행성 근이영양증 Types of PMD(Progressive Muscular Dystroph... |
| TAPVR | Total Anomalous Pulmonary Venous Return = TAPVC 4 Types of TAPVR &... |
| NFJ | Naegeli-Franceschetti-Jadassohn [syndrome] |
| ALL | Acute Lymphocytic Leukemia 형태학적 분류 L1; Small, Homogenous(... |
| AMoL | Acute monocytic leukaemia |
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| M5 | monocytic leukaemia |
| HME | Human monocytic ehrlichiosis |
| AMML | acute myelo-monocytic leukemia |
| M4 | myelo-monocytic leukemia |
acute monocytic leukemia
| Naegeli type of monocytic leukaemia | A variant of granulocytic leukaemia with monocytosis in the peripheral blood. Synonym: Naegeli type of monocytic leukaemia. (05 Mar 2000) |
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| Schilling type of monocytic leukaemia | See: monocytic leukaemia. (05 Mar 2000) |
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| acute monocytic leukaemia | <haematology> The most common translocation in this disorder of poorly differentiated monocytic cells involves chromosome region 11q in a large percentage of cases. The translocation involves a cellular oncogene, c-ets which is mapped to the 11q23-24 region. The most common translocations reported are t(6;11), t(9;11), t(11;17) and t(11;19), of which t(9;11) (p21-22;q23) is by far the most frequently detected and implicated in acute myeloid leukaemia. The cells express CD14 surface antigen, which is diagnostic of monocytic cells. Acronym: AML Classification: FAB M5 (07 Apr 1998) |
| monocytic leukaemia | Cancer of the blood due to proliferation of cells of the monocyte series. Origin: Gr. Haima = blood (13 Nov 1997) |
| Naegeli, Oskar | <person> Swiss physician, 1885-1959. See: Naegeli syndrome. (05 Mar 2000) |
| Naegeli, Otto | <person> Swiss physician, 1871-1938. See: Naegeli type of monocytic leukaemia. (05 Mar 2000) |
| Naegeli syndrome | <syndrome> Reticular skin pigmentation, diminished sweating, hypodontia, and hyperkeratosis of the palms and soles; may be confused with incontinentia pigmenti but is as common in males as in females; autosomal dominant inheritance. Synonym: Franceschetti-Jadassohn syndrome. (05 Mar 2000) |
| monocytic angina | An obsolete term for infectious mononucleosis. (05 Mar 2000) |
| monocytic leukemoid reaction | Leukocytosis of varying degree, e.g., 30,000 to 40,000 per cu mm, with adult monocytes and immature forms amounting to 30% (or more) of the total number of white blood cells in the circulating blood; may be observed in association with tuberculosis, especially the first infection, miliary type. (05 Mar 2000) |
| monocytic leukocytosis | An abnormal increase in the number of monocytes in the circulating blood. Synonym: monocytic leukocytosis. (05 Mar 2000) |
| monocytic leukopenia | Diminution in the number of monocytes in the circulating blood. Synonym: monocytic leukopenia, monopenia. Origin: mono-+ G. Kytos, cell, + penia, poverty (05 Mar 2000) |
| equine monocytic ehrlichiosis | <veterinary> A febrile disease of horses in North America caused by Ehrlichia risticii and characterised by anorexia, leukopenia, and occasional diarrhoea. Synonym: Potomac horse fever. (05 Mar 2000) |
| abelson leukaemia virus | A defective murine leukaemia virus capable of transforming lymphoid cells and producing a rapidly progressing lymphoid leukaemia after superinfection with friend, moloney, or rauscher virus. (12 Dec 1998) |
| Abelson murine leukaemia virus | A retrovirus belonging to the Type C retrovirus group subfamily (family Oncovirinae) which is associated with leukaemia and produces in vitro transformation of mouse cells. (05 Mar 2000) |
| accelerated phase of leukaemia | Refers to chronic myelogenous leukaemia that is progressing. The number of immature, abnormal white blood cells in the bone marrow and blood is higher than in the chronic phase, but not as high as in the blast phase. (12 Dec 1998) |
| acute granulocytic leukaemia | <haematology> A form of leukaemia which is characterised by the proliferation of 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. Treatment includes chemotherapy and/or bone marrow transplant. Origin: Gr. Haima = blood (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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