| ¿µ¹® | keratosis | ÇÑ±Û | °¢ÈÁõ |
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| ¼³¸í | ÇǺΠǥÇÇÀÇ ÃÖ»óÃþ¿¡ ÀÖ´Â °¢ÁúÃþÀÌ Áõ½Ä-º¯ÈÇÏ¿© ±îÄ¥±îÄ¥ÇØÁö°Å³ª ±»¾îÁö´Â ÇǺκ´-Ç¥ÇÇÀÇ °¢ÁúÀÌ Áõ½ÄÇÒ »Ó¸¸ ¾Æ´Ï¶ó, ¶§·Î´Â ÅÐÁÖ¸Ó´ÏÀÇ °¢ÃþÀÌ Ç¥ÇÇÀÇ °¢Ãþº¸´Ùµµ ½ÉÇÏ°Ô Áõ½ÄÇÏ¿© ±¸ÁøÀ» Çü¼ºÇÏ´Â ¼ö°¡ ÀÖ´Ù. °¢ÁúÀº Ç¥ÇǼ¼Æ÷°¡ °¢ÈÇÏ¿© »ý±â´Â °ÍÀ¸·Î, Á¤»óÀûÀÎ °¢È°úÁ¤¿¡¼´Â °¢Ãþ¿¡ ¼¼Æ÷ÇÙÀ» ¹ß°ßÇÒ ¼ö ¾ø´Ù. ±×·±µ¥ °¢ÁúÁõ½ÄÀÇ °æ¿ì¿¡´Â ¼¼Æ÷ÇÙÀÌ Àß ¿°»öµÇ¾î Á¸ÀçÇÑ´Ù. |
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| ¿µ¹® | actinic keratosis | ÇÑ±Û | ±¤¼±°¢ÈÁß |
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| ¼³¸í | Àϱ¤°¢ÈÁõ, ³ëÀμº°¢ÈÁõ µîÀ¸·Î ºÒ¸®´Â ÀÌ º´Àº ž翡 ³ëÃâµÇ´Â ºÎÀ§¿¡ ³ªÅ¸³ª´Â 1cm ÀÌÇÏÀÇ È«¹Ý¼º °¢È±¸ÁøÀÌ´Ù. Áï ºÓÀº »öÀ» ¶ì´Â ²®ÁúÀÌ ÀϾ´Â ¸ð¾çÀ» ÇÑ À¶±â°¡ ¾à°£ ÀÖ´Â ±×¸®°í °æ°è°¡ ºñ±³Àû ¸íÈ®ÇÑ µÕ±Ù ¸ð¾çÀÇ º´ÅÍÀÌ´Ù. ÀÌ º´Àº ´ë°³ ÇÞºµ³ëÃâÀ̳ª ÇǺÎÀÇ »öÁ¶¿Í »ó°üÀÖ°í ¾à 20%¿¡¼ ÆíÆò¼¼Æ÷¾ÏÁ¾ÀÇ ¹ß»ýÀÌ ÀÖ¾î Ä¡·á¸¦ ÇÊ¿ä·Î ÇÑ´Ù. |
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| SK | seborrheic keratosis; senile keratosis; Sloan-Kettering [Institute for Cancer Research]; spontaneous... |
|---|---|
| CDF | chondrodystrophia foetalis |
| IPK | intractable plantar keratosis |
| KFSD | keratosis follicularis spinulosa decalvans |
| LK | left kidney; lichenoid keratosis; lymphokine |
| KFSD | Keratosis follicularis spinulosa decalvans |
|---|---|
| SK | Seborrheic keratosis |
| keratosis diffusa foetalis | most common form of ichthyosis characterised by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autosomal dominant trait. (12 Dec 1998) |
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| placenta diffusa | An abnormally thin placenta covering an unusually large area of the uterine lining. Synonym: placenta diffusa. (05 Mar 2000) |
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| psoriasis diffusa | Diffused psoriasis, a form of psoriasis with extensive coalescence of the lesions. (05 Mar 2000) |
| encephalitis periaxialis diffusa | Term used to describe at least two separate disorders described by Schilder: 1) Diffuse sclerosis or encephalitis periaxialis diffusa; a nonfamilial disorder affecting primarily children and young adults and characterised by progressive dementia, visual disturbances, deafness, pseudobulbar palsy, and hemiplegia or quadriplegia. Most patients die within a few years of onset; pathologically, there is a large, asymmetrical area of myelin destruction, sometimes involving an entire cerebral hemisphere, and typically with extension across the corpus callosum. 2) The leukodystrophies. Synonym: encephalitis periaxialis diffusa, Flatau-Schilder disease. (05 Mar 2000) |
| leishmaniasis tegumentaria diffusa | Leishmaniasis caused by several New and Old World species and strains of Leishmania (L. Mexicana amazonensis, L. M. Pifanoi, possibly L. M. Garnhami and L. M. Venezuelensis; in Ethiopia, L. Aethiopica, and unidentified leishmanial agents in Namibia and Tanzania). The condition is associated with a suppressed cell-mediated immune response, so that the non-ulcerating, non-necrotizing cutaneous lesions can spread widely over the body; great numbers of parasite-filled macrophages are found in the dermal lesions. Healing does not appear to occur unless an acquired cellular hypersensitivity can develop. Synonym: anergic leishmaniasis, diffuse leishmaniasis, disseminated cutaneous leishmaniasis, leishmaniasis tegumentaria diffusa, pseudolepromatous leishmaniasis. (05 Mar 2000) |
| rachitis foetalis | congenital rickets |
| rachitis foetalis annularis | Congenital enlargement of the epiphyses of the long bones. (05 Mar 2000) |
| rachitis foetalis micromelica | A congenital condition in which development of the long bones is deficient. (05 Mar 2000) |
| pars foetalis placentae | <embryology> Placenta foetalis, the chorionic portion of the placenta, containing the foetal blood vessels, from which the funis develops; specifically, in humans, it develops from the chorion frondosum. Synonym: pars foetalis placentae. (05 Mar 2000) |
| chondromalacia foetalis | An intrauterine form of chondromalacia in which the foetus is born dead with soft pliable limbs. (05 Mar 2000) |
| hydrops foetalis | <embryology, paediatrics> A severe form of the genetic disorder thalassaemia in which all four alpha chain polypeptides making up the haemoglobin molecule (the protein which transports oxygen in the body) are missing due to a defect in the gene which codes for them. As a result, affected individuals die at or before birth. (09 Oct 1997) |
| ichthyosis foetalis | Recessive condition in Holstein and Norwegian red poll cattle resembling harlequin foetus in humans. See: harlequin foetus (05 Mar 2000) |
| erythroblastosis foetalis | <haematology> A condition which develops in the foetus due to an incompatibility between the mother's blood type (RH factor) and the baby's. Maternal antibodies, which enter the foetal circulation during delivery attack the baby's red blood cells leading to haemolysis (rupture of the cells). Symptoms include an infant with an enlarged liver and spleen, swelling, jaundice and anaemia. (27 Sep 1997) |
| actinic keratosis | <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) |
| arsenical keratosis | Multiple keratoses, most commonly of the palms and soles but also of the fingers and proximal portions of the extremities, resulting from long-term arsenic ingestion; they resemble Bowen's disease microscopically and may become malignant. (05 Mar 2000) |
| seborrheic keratosis | A benign skin lesion resulting from excessive growth of the top layer of skin cells. It usually is found in persons over 30 years old and may be few or numerous. (12 Dec 1998) |
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