| ¿µ¹® | keratosis | ÇÑ±Û | °¢ÈÁõ |
|---|---|---|---|
| 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. |
||
| ¿µ¹® | actinic keratosis | ÇÑ±Û | ±¤¼±°¢ÈÁß |
|---|---|---|---|
| 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. |
||
| SK | seborrheic keratosis; senile keratosis; Sloan-Kettering [Institute for Cancer Research]; spontaneous... |
|---|---|
| IPK | intractable plantar keratosis |
| KFSD | keratosis follicularis spinulosa decalvans |
| LK | left kidney; lichenoid keratosis; lymphokine |
| PPK | palmoplantar keratosis; prekallikrein |
| RCDP | Rhizomelic Chondrodysplasia Punctata |
|---|---|
| KFSD | Keratosis follicularis spinulosa decalvans |
| SK | Seborrheic keratosis |
| keratosis punctata | Horny papules over the palms, soles, and digits that develop central plugs; seen commonly in blacks. Synonym: keratoma disseminatum, keratosis punctata. (05 Mar 2000) |
|---|
| acne punctata | Acne with black open comedones. (05 Mar 2000) |
|---|---|
| retinopathy punctata albescens | A disease in which both fundi show numerous white dots through the retina; causes night blindness. (05 Mar 2000) |
| chondrodysplasia punctata | A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (chondrodysplasia punctata, rhizomelic), an autosomal dominant form (conradi-hunermann syndrome), and a milder x-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form. (12 Dec 1998) |
| chondrodysplasia punctata, rhizomelic | An autosomal recessive form of chondrodysplasia punctata characterised by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondrial bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata. (12 Dec 1998) |
| chondrodystrophia congenita punctata | Congenital shortening of the humerus and femur, with stippled epiphyses, high-arched palate, cataracts, erythroderma in the newborn, and scaling followed by follicular atrophoderma; there is also an autosomal dominant inheritance pattern . Synonym: chondrodystrophia congenita punctata. (05 Mar 2000) |
| Cooperia punctata | Species that occurs mainly in cattle, less commonly in sheep, water buffalo, and several wild ruminants; although worldwide in distribution, it is especially widespread in North America and common in Hawaii. Synonym: Cooperia fieldingi. (05 Mar 2000) |
| Haemaphysalis cinnabarina punctata | A race of Haemaphysalis in Europe, north Africa, and Japan; larvae and nymphs feed on terrestrial reptiles, and adults on various domestic herbivores, rabbits, and hedgehogs; it transmits bovine babesiosis and anaplasmosis. (05 Mar 2000) |
| psoriasis punctata | Psoriasis in which the individual lesions are papules, each red in colour, and tipped with a single white scale. (05 Mar 2000) |
| dysplasia epiphysialis punctata | A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form. Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis. (05 Mar 2000) |
| 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) |
| senile 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) |
| solar keratosis | 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) |
| nevus follicularis keratosis | Comedo nevus, congenital or childhood linear keratinous cystic invaginations of the epidermis, with failure of development of normal pilosebaceous follicles. Synonym: nevus follicularis keratosis. (05 Mar 2000) |
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|