| ¿µ¹® | purpura | ÇÑ±Û | ÀÚ»ö¹ÝÁõ |
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| ¼³¸í | ÇǺγ»ÀÇ ÃâÇ÷·Î ÀÎÇÏ¿©, ÇǺΠǥÇǸ¦ ÅëÇÏ¿© ½±°Ô º¸ÀÌ´Â ÀÚÈ«»ö ȤÀº Àû°¥»ö ¹ÝÁ¡À» Ư¡À¸·Î ÇÏ´Â ÀÏ·ÃÀÇ ÁúȯÀ» ÃÑĪÇÏ´Â ¿ë¾îÀÌ´Ù. ´ë°³ È«¹Ý°ú ±¸º°ÇØ¾ß ÇÏ´Â µ¥ È«¹ÝÀº ÇǺιØÀÇ Ç÷°üÀÌ ÆØÃ¢ÇÏ¿© ºÓ°Ô º¸ÀÌ´Â Çö»óÀ¸·Î Åõ¸íÇÑ ÀÚ¸¦ ÀÌ¿ëÇÏ¿© ÇǺθ¦ ´·¯¼ °üÂûÇØº¸¸é ½±°Ô ±¸º°ÀÌ °¡´ÉÇÏ´Ù. À̶§ È«¹ÝÀº ºÓÀº »öÀÌ ¾ø¾îÁöÁö¸¸, ÀÚ¹ÝÀº ºÓÀº »öÀÌ ¾ø¾îÁöÁö ¾Ê´Â´Ù. |
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| ITP | idiopathic thrombocytopenic purpura; immune thrombocytopenia; immunogenic thrombocytopenic purpura; ... |
|---|---|
| ATP | 1) Adenosine Tri-Phosphate 2) Autoimmune Thrombocytopenic Purpura |
| HSP | Henoch Schonlein Purpura |
| ITP | Idiopathic(Immune) Thrombocytopenic Purpura |
| PTP | Post-Transfusion Purpura |
| AITP | Autoimmune thrombocytopenic purpura |
|---|---|
| ATP | Autoimmune thrombocytopenic purpura |
| HSP | Henoch Schonlein Purpura |
| HSPN | Henoch-Schoenlein purpura nephritis |
| ITP | Idiopathic thrombocytopenic purpura |
| purpura senilis | The occurrence of petechiae and ecchymoses on the atrophic skin of the legs in aged and debilitated subjects. (05 Mar 2000) |
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| alopecia senilis | The normal loss of scalp hair in old age. (05 Mar 2000) |
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| arcus senilis | <clinical sign, ophthalmology> An opaque ring around the iris (coloured portion of the eye), seen most often in elderly people. (27 Sep 1997) |
| vaginitis senilis | senile vaginitis |
| malum articulorum senilis | <rheumatology> Arthritis in the aged. (05 Mar 2000) |
| verruca plana senilis | <dermatology> A skin lesion that is abnormally sensitive to the effects of ultraviolet light (sunlight). Thought to be a precancerous skin lesion that is more common in the fair-skinned or elderly individual. Approximately 20% of these skin lesions will develop into squamous cell carcinoma. Prevention includes the use of sun screen agents and the avoidance of drugs (for example tetracyclines) known to cause photosensitivity reactions. Usually a discreet slightly raised, red or pink lesion located on a sun exposed surface. Texture may appear as rough, gritty or scaly. Growths may be biopsied to look for cancer or removed via cryotherapy or electrical cautery. Some topical agents may be used to promote peeling. (27 Sep 1997) |
| verruca senilis | <dermatology> A skin lesion that is abnormally sensitive to the effects of ultraviolet light (sunlight). Thought to be a precancerous skin lesion that is more common in the fair-skinned or elderly individual. Approximately 20% of these skin lesions will develop into squamous cell carcinoma. Prevention includes the use of sun screen agents and the avoidance of drugs (for example tetracyclines) known to cause photosensitivity reactions. Usually a discreet slightly raised, red or pink lesion located on a sun exposed surface. Texture may appear as rough, gritty or scaly. Growths may be biopsied to look for cancer or removed via cryotherapy or electrical cautery. Some topical agents may be used to promote peeling. (27 Sep 1997) |
| pruritus senilis | Senile pruritus, itching associated with dryness of the skin in the aged. (05 Mar 2000) |
| linea corneae senilis | An opaque, grayish ring at the periphery of the cornea just within the sclerocorneal junction, of frequent occurrence in the aged; it results from a deposit of fatty granules in, or hyaline degeneration of, the lamellae and cells of the cornea. Synonym: anterior embryotoxon, arcus adiposus, arcus juvenilis, arcus lipoides, arcus senilis, gerontoxon, linea corneae senilis, lipoidosis corneae. (05 Mar 2000) |
| acute vascular purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| allergic purpura | Nonthrombocytopenic purpura due to sensitization to foods, drugs, and insect bites. Synonym: anaphylactoid purpura. (05 Mar 2000) |
| anaphylactoid purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| autoimmune thrombocytopenia purpura | <haematology> A rare autoimmune disorder characterised by an acute shortage of platelets with resultant bruising and spontaneous bleeding. The platelet count becomes exceedingly low and spontaneous bleeding from the gums, gastrointestinal tract and nose can be seen. Physical examination may demonstrate enlargement of the spleen. A typical rash occurs to do microscopic haemorrhage of small blood vessels in the skin. Platelet counts under 10,000 can lead to spontaneous haemorrhage into the brain causing death. Treatment with corticosteroids is generally effective. Surgical removal of the spleen (splenectomy) is reserved for some patients. Anti-platelet antibodies are detectable in some cases. It may present in either an acute or a chronic form. Acronym: ITP (20 Sep 2002) |
| Waldenstrom's purpura | <haematology> A condition characterised by proliferation of cells resembling lymphocytes or plasma cells in the bone marrow, anaemia, increased sedimentation rate and hyperglobulinaemia. Physical findings include mucosal bleeding, skin purpura and enlargement of the lymph nodes, liver and spleen. (27 Sep 1997) |
| Henoch-Schonlein purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
| Henoch's purpura | <dermatology> This relatively rare disorder is characterised by skin purpura, joint pains, abdominal pain and renal disease (glomerulonephritis). Although Henoch-Schonlein purpura or anaphylactoid purpura, is thought to be a immune complex mediated disease, its exact cause is unknown. Its typical benign coarse can, however, include renal failure. (27 Sep 1997) |
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