| HMR | histiocytic medullary reticulosis |
|---|---|
| LFR | lymphoid follicular reticulosis |
| HLH | helix-loop-helix; hemophagocytic lymphohistiocytosis |
| IAHS | infection-associated hemophagocytic syndrome; International Association of Hospital Security |
| VAHS | virus-associated hemophagocytic syndrome |
| IAHS | Infection-Associated Hemophagocytic Syndrome |
|---|---|
| HMR | Histiocytic medullary reticulosis |
| MMR | Midline malignant reticulosis |
| PR | Polymorphic reticulosis |
| BFNC | Benign Familial Neonatal Convulsions |
omemtulum
Omenns syndrome : 동의어=histiocytic medullary reticulosis.
omental
| benign inoculation reticulosis | <disease> A self-limiting bacterial infection of the regional lymph nodes (lymphadenitis) caused by afipia felis, a gram-negative bacterium recently identified as bartonella henselae. It usually arises one or more weeks following a feline scratch, with raised inflammatory nodules at the site of the scratch being the primary symptom. It results in tender and enlarged lymph glands above the site of injury. A chronic benign adenopathy, especially in children and young adults, commonly associated with a recent cat scratch or bite and caused by bacteria including Bartonella henselae and Alipia felis; the lymphadenopathy usually resolves spontaneously within a period of several months, but complications involving central nervous system, liver, spleen, lung, and skin have been seen. Synonym: benign inoculation lymphoreticulosis, benign inoculation reticulosis, cat-scratch fever, regional granulomatous lymphadenitis. (05 Mar 2000) |
|---|---|
| pagetoid reticulosis | A benign localised form of lymphoma with solitary or closely grouped cutaneous tumours consisting of predominantly epidermal infiltration of mononuclear cells resembling those found in mycosis fungoides. Synonym: pagetoid reticulosis. (05 Mar 2000) |
| malignant midline reticulosis | An obsolete term for polymorphic reticulosis (05 Mar 2000) |
| reticulosis | 1. An increase in histiocytes, monocytes, or other reticuloendothelial elements. 2. Obsolete term for lymphoma. Origin: reticulo-+ G. -osis, condition (05 Mar 2000) |
| midline malignant reticulosis granuloma | Destruction of the nasal septum, hard palate, lateral nasal walls, paranasal sinuses, skin of the face, orbit and nasopharynx by an inflammatory infiltrate with atypical lymphocytic and histiocytic cells; presumably a form of lymphoma in most cases. An obsolete term for polymorphic reticulosis. Synonym: granuloma gangrenescens, malignant granuloma, midline malignant reticulosis granuloma. (05 Mar 2000) |
| polymorphic reticulosis | A necrotizing lymphoproliferative lesion with a predilection for the upper respiratory tract. Previously called lethal midline granuloma or malignant midline reticulosis. Treatment is irradiation. (05 Mar 2000) |
| leukaemic reticulosis | Cancer of the blood due to proliferation of cells of the monocyte series. Origin: Gr. Haima = blood (13 Nov 1997) |
| lipomelanic reticulosis | Enlargement of lymph nodes, with proliferation of pale-staining interdigitating reticulum cells and macrophages containing fat and melanin; secondary to various forms of dermatitis. Synonym: dermatopathic lymphadenitis, lipomelanic reticulosis. (05 Mar 2000) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
| cancer, breast, familial | A number of factors have been identified that increase the risk of breast cancer. One of the strongest of these risk factors is the history of breast cancer in a relative. About 15-20% of women with breast cancer have such a family history of the disease, clearly reflecting the participation of inherited (genetic) components in the development of some breast cancers. Dominant breast cancer suceptibility genes, including BRCA1 and BRCA2, appear responsible for about 5% of all breast cancer. (12 Dec 1998) |
| paralysis, familial periodic | An autosomal dominant trait marked by recurring attacks of rapidly progressive flaccid paralysis. There are three types: I, associated with a fall in serum potassium levels (hypokalaemic periodic paralysis); II, associated with a rise therein (hyperkalaemic periodic paralysis, called also adynamia episodica hereditaria); and III, with normal levels (normokalaemic periodic paralysis). (12 Dec 1998) |
| pemphigus, benign familial | Rare hereditary disease characterised by recurrent eruptions of vesicles and bullae mainly on the neck, axillae, and groin. It exhibits autosomal dominant inheritance and is unrelated to pemphigus vulgaris though it closely resembles that disease. (12 Dec 1998) |
| chronic familial icterus | <haematology> A hereditary disorder that leads to a chronic haemolytic anaemia due to an abnormality in the red blood cell membrane. This disorder is caused by a defective gene. Red cells are resistant to stress and rupture easily. Infants may appear jaundiced and pale. Fatigue, weakness and shortness of breath are other symptoms that may be seen in older patients. The spleen may also be enlarged. Treatment includes splenectomy (removal of the spleen). After this is accomplished the life-span of the red blood cells returns to normal. (27 Sep 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|