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"hereditary progressive mucinous histiocytosis X"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
¾Ë±â½¬¿î ÀÇÇпë¾îÇ®ÀÌÁý, ¼­¿ïÀÇ´ë ±³¼ö ÁöÁ¦±Ù, °í·ÁÀÇÇÐ ÃâÆÇ À¯»ç °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
¿µ¹® mucinous tumor ÇÑ±Û Á¡¾×Á¾¾ç
¼³¸í   
  Á¡¾×À¸·Î ±¸¼ºµÈ Á¾¾çÀ» ¸»Çϴµ¥ ÁַΠ¿©¼ºÀÇ ³­¼Ò¿¡¼­ ¹ß»ýÇϴ ³¶¼º(¹°ÁָӴϰ°Àº Á¾¾çÀ» ¸»ÇÔ) Á¾¾ç¿¡¼­ ¸¹ÀÌ º¼ ¼ö ÀÖ´Ù.
´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • histiocytosis
    Á¶Á÷±¸Áõ
  • Langerhans cell histiocytosis
    ¶û°Ô¸£Çѽº¼¼Æ÷Á¶Á÷±¸Áõ
  • mucinous
    Á¡¾×-
  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾
  • mucinous cystadenoma
    Á¡¾×³¶»ùÁ¾
  • congenital hereditary hearing loss
    ¼±ÃµÀ¯Àü³­Ã»
  • hereditary
    À¯Àü-
  • hereditary ataxia
    À¯Àü½ÇÁ¶
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¾ç¼º»óÇdz»ÀÌ»ó°¢È­Áõ
  • hereditary cerebellar ataxia
    À¯Àü¼Ò³ú½ÇÁ¶
  • hereditary chorea
    À¯Àü¹«µµº´
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hereditary coproporphyria
    À¯ÀüÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ
  • hereditary disease
    À¯Àüº´
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
´ëÇÑÀÇÇù Çʼö ÀÇÇпë¾îÁý »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 7 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • mucinous cystadenoma
    Á¡¾×³¶»ùÁ¾
  • histiocytosis
    Á¶Á÷±¸Áõ
  • rapidly progressive glomerulonephritis
    ±Þ¼ÓÁøÇàÅ丮ÄáÆÏ¿°, ±Þ¼ÓÁøÇà»ç±¸Ã¼½Å¿°
  • progressive bulbar palsy
    ÁøÇà¼û³ú¸¶ºñ, ÁøÇ࿬¼ö¸¶ºñ
  • hereditary
    À¯Àü-
  • hereditary motor sensory neuropathy
    À¯Àü¿îµ¿°¨°¢½Å°æº´Áõ
  • hereditary spherocytosis
    À¯ÀüµÕ±ÙÀûÇ÷±¸Áõ, À¯Àü±¸ÇüÀûÇ÷±¸Áõ
¿¾ ´ëÇÑÀÇÇù ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • histiocytosis
    Á¶Á÷±¸Áõ
  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾
  • mucinous exudate
    Á¡¾×»ïÃâ¹°
  • mucinous syringometaplasia
    Á¡¾×¶¡°üÈ­»ý
  • hereditary ataxia
    À¯ÀüÁ¶È­¿îµ¿ºÒ´É
  • congenital hereditary hearing loss
    ¼±ÃµÀ¯Àü³­Ã»
  • hereditary chorea
    À¯Àü¹«µµº´
  • hereditary coproporphyria
    À¯ÀüÄÚÇÁ·ÎÆ÷¸£ÇǸ°Áõ
  • hereditary methemoglobinemic cyanosis
    À¯Àü¸ÞÆ®Çì¸ð±Û·ÎºóÇ÷û»öÁõ
  • hereditary disease
    À¯Àüº´
  • hereditary disorder
    À¯ÀüÀå¾Ö, À¯ÀüÁúȯ
  • hereditary benign intraepithelial dyskeratosis
    À¯Àü¾ç¼º»óÇdz»ÀÌ»ó°¢È­Áõ
  • hereditary coagulation disorder
    À¯ÀüÀÀ°íÀå¾Ö
  • hereditary opalescent dentine
    À¯ÀüÀ¯¹é»ö»ó¾ÆÁú
  • recessive hereditary disease
    ¿­¼ºÀ¯Àüº´
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hereditary progressive mucinous histiocytosis X
    À¯Àü¼º ÁøÇ༺ Á¡¾×¼ºÁ¶Á÷±¸Áõ
¿¾ ´ëÇÑÀÇÇù 2 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • Langerhans cell histiocytosis
    ¶û°Ô¸£Çѽº ¼¼Æ÷ Á¶Á÷±¸Áõ
  • Langerhans cell histiocytosis
    ¶û°Ô¸£Çѽº¼¼Æ÷Á¶Á÷±¸Áõ
  • hematophagic histiocytosis
    ½ÄÇ÷¼º Á¶Á÷±¸Áõ
  • histiocytosis
    Á¶Á÷±¸Áõ
  • histiocytosis
    Á¶Á÷±¸Áõ.(ðÚòÄϹñø)
  • histiocytosis X
    XÁ¶Á÷±¸Áõ.
  • histiocytosis X
    XÁ¶Á÷±¸Áõ
  • histiocytosis syndrome
    Á¶Á÷±¸Áõ ÁõÈıº.
  • histiocytosis,generalized
    Àü½Å¼º(îïãóàõ)
  • histiocytosis,malignant
    ¾Ç¼º
  • histiocytosis,sinus
    (Á¤¸Æ)µ¿
  • acquired progressive lymphangioma
    ÈÄõ¼º ÁøÇ༺ ¸²ÇÁ°üÁ¾
  • infantile progressive spinal muscular atrophy
    ¿µ¾ÆÁøÇ༺ ô¼ö¼º ±ÙÀ§Ãà(Áõ).
  • progressive
    ÁøÇ༺
  • progressive
    ÁøÇ༺ÀÇ(òäú¼àõ¡­), Á÷Áø(¼º)ÀÇ(òÁòä(àõ)¡­)
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú : 1 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hereditary progressive mucinous histiocytosis X
    À¯Àü¼º ÁøÇ༺ Á¡¾×¼ºÁ¶Á÷±¸Áõ
¿¾ ´ëÇÑÀÇÇù 3 ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • breast,carcinoma colloid or mucinous
    Á¡¾×¼º (ïÄäûàõ)
  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾(¡­¾ÏÁ¾).
  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾(¡­äßðþ)
  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾(¡­äßðþ).
  • mucinous corneal degeneration
    Á¡¾×°¢¸·º¯¼º
  • mucinous eccrine carcinoma
    Á¡¾×¼º ÇѼ± ¾ÏÁ¾
  • mucinous exudate
    Á¡¾×»ó »ïÃâ¾×(¡­ßÒß¶õóäû).
  • mucinous syringometaplasia
    Á¡¾×¼º ÇѰü ÀÌÇü¼ºÁõ
  • mucinous tumor
    Á¡¾×¼º Á¾¾ç(¡­àõ ðþåË)
  • atypical regressing histiocytosis X
    ÅðÇ༺ ºñÀüÇü Á¶Á÷±¸Áõ
  • benign cephalic histiocytosis
    ¾ç¼º µÎºÎÁ¶Á÷±¸Áõ
  • hematophagic histiocytosis
    ½ÄÇ÷¼º Á¶Á÷±¸Áõ
  • histiocytosis
    Á¶Á÷±¸Áõ
  • histiocytosis
    Á¶Á÷±¸Áõ.(ðÚòÄϹñø)
  • histiocytosis X
    XÁ¶Á÷±¸Áõ
´ëÇÑ»ýÈ­ÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 2 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hereditary code
    À¯Àü ºÎÈ£(ë¶îîݬûÜ)
  • hereditary material
    À¯Àü ¹°Áú(ë¶îîÚªòõ)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 12 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • histiocytosis X
    XÁ¶Á÷±¸Áõ
  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾
  • hereditary
    À¯Àü¼ºÀÇ
  • hereditary craniofacial dysostosis
    À¯Àü¼ºµÎ°³¾È¸éÀ̰ñÁõ
  • hereditary disease
    À¯Àüº´
  • hereditary ectodermal polydysplasia
    À¯Àü¼º¿Ü¹è¿±¼º´Ù¹ßÀÌÇü¼ºÁõ
  • hereditary hemorrhagic telangiectasia
    À¯Àü¼ºÃâÇ÷¼º¸ð¼¼Ç÷°üÈ®Àå
  • progressive
    ÁøÇ༺ÀÇ, ÁøÁ÷(¼º)ÀÇ
  • progressive diaphyseal dysplasia
    ÁøÇ༺°ñ°£¼ºÀÌÇü¼º(Áõ)
  • progressive multifocal leukoencephalopathy
    ÁøÇ༺´ÙÃÊÁ¡¼º¹éÁú³úº´Áõ
  • progressive muscle dystrophy
    ÁøÇ༺±ÙÀÌ¿µ¾çÁõ
  • progressive spinal amyotrophy
    ÁøÇ༺ô¼ö¼º±ÙÀ§ÃàÁõ
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
OCAA Ovarian Cystadenocarcinoma Associated Antigen; Serous Mucinous Ovarian Tumor¿¡¸¸ ³ªÅ¸³²
PMD Progressive Muscular Dystrophy; ÁøÇ༺ ±ÙÀÌ¿µ¾çÁõ
  Types of PMD(Progressive Muscular Dystroph...
PML peripheral motor latency; polymorphonuclear leukocyte; posterior mitral leaflet; progressive multifo...
PR by way of the rectum [Lat. per rectum]; far point [of accommodation] [Lat. punctum remotum]; palindr...
PSS painful shoulder syndrome; physiologic saline solution; porcine stress syndrome; primary Sjogren syn...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
histiocytosis X histiocytosis
IPMT Intraductal papillary mucinous tumor
HX Histiocytosis X
LCH Langerhans Cell Histiocytosis
MH Malignant Histiocytosis
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • mucinous breast carcinoma
    Á¡¾×¼º À¯¹æ ¾Ï
  • histiocytosis syndrome
    Á¶Á÷±¸Áõ ÁõÈıº
  • histiocytosis-x
    Á¶Á÷±¸ Áõ½ÄÁõ
  • idiopathic histiocytosis
    Ư¹ß¼º Á¶Á÷±¸Áõ, Ư¹ß¼º Á¶Á÷±¸ Áõ½ÄÁõ
    ÀÌÀü¿¡´Â Á¶Á÷±¸ Áõ½ÄÁõ X¶ó°í ºÒ·¶À¸¸ç ±âº»ÀûÀÎ º´º¯Àº ¼¼¸Á ³»ÇÇ ¼¼Æ÷ÀÇ Áõ½ÄÀÌ¸ç ¹ßº´ ¿¬·É ¹× ¿¹ÈÄ¿¡ µû¶ó Letterer-Siwe Áúȯ, Hand-schuller-christian Áúȯ, È£»ê¼º À°¾ÆÁ¾À¸·Î ºÐ·ùÇÑ´Ù.
  • hereditary
    À¯Àü¼º
    ºÎ¸ð·ÎºÎÅÍ ´ÙÀ½ ¼¼´ë·Î À¯ÀüÀÚ¿¡ ÀÇÇØ Àü´ÞµÇ´Â.
  • hereditary amyloidosis
    À¯Àü¼º À¯ÀüºÐÁõ
    1. À¯Àü¿¡ ÀÇÇØ ¿ø¼¶À¯¼º ´ç ´Ü¹éÀÌ ÇǺÎ, Á¡¸·, ³»ºÎ Àå±â¿¡ ħÀüµÇ´Â º´. 2. À¯ÀüÀûÀ¸·Î ½ÅüÀÇ °¢Á¾ ºÎÀ§¿¡ ¾Æ¹Ð·ÎÀ̵å
  • hereditary angioedema
    À¯Àü¼º ¸Æ°ü ºÎÁ¾, À¯Àü¼º Ç÷°ü ºÎÁ¾
    ½ÉºÎÀÇ ÁøÇÇ, ÇÇÇÏ Á¶Á÷, Á¡¸·ÇÏÁ¶Á÷À» ħ½ÀÇÏ´Â Ç÷°ü ¹ÝÀÀÀ¸·Î¼­, ¸ð¼¼Ç÷°üÀÇ È®Àå°ú Åõ°ú¼º Ç×Áø¿¡ ÀÇÇØ ÀϾ´Â ±¹ÇѼº ºÎÁ¾À» ³ªÅ¸³»¸ç °Å´ëÇÑ ÆØÁøÀÇ ¹ß»ýÀ» Ư¡À¸·Î ÇÑ´Ù. »ó¿°»öü¼º ¿ì¼º ÇüÁú·Î À¯ÀüÇÑ´Ù. »ê¹ß¼ºº¸´Ù ³»Àå º´º¯À» ´õ Àß ÀÏÀ¸Å°´Â °æÇâÀÌ ÀÖ´Ù.
  • hereditary aphasia
    À¯Àü ½Ç¾î, À¯Àü¼º ½Ç¾î, À¯Àü ½Ç¾îÁõ, À¯Àü¼º ½Ç¾îÁõ
  • hereditary brown tooth
    À¯Àü¼º °¥»ö Ä¡¾Æ
  • hereditary cerebrospinal paralysis
    ¿ìÀü¼º ³úô¼ö ¸¶ºñ
    º¸Åë Áß³â Ãʱ⿡ ÁøÇàÇÏ´Â À¯Àü¼º ÁúȯÀ¸·Î »óÁö ¶Ç´Â ÇÏÁöÀÇ ¾çÁö ¶Ç´Â ÀÏÃøÀ̳ª »çÁö¿¡ ³ªÅ¸³ª¸ç, ¼­¼­È÷ ÁøÇàµÇ´Â ¸¶ºñ°¡ Ư¡ÀÌ´Ù.
  • hereditary craniofacial dysostosis
    À¯Àü¼º µÎ°³ ¾È¸é À̰ñÁõ
    ž»ó µÎ°³, ¾È±¸ µ¹Ãâ, ¾ç¾È °Ý¸®, »ç½Ã, ¾Þ¹«»õ ºÎ¸® ¸ð¾ç1114-377786/377786Àüµ¹À» ¼ö¹ÝÇÏ´Â »ó¾Ç Çü¼º ºÎÀüÀ» Ư¡À¸·Î ÇÏ´Â À¯ÀüÀû Áúȯ.
  • hereditary disease
    À¯Àüº´
    À¯ÀüÀÚ¿¡ ÀÇÇÏ¿© ÀϾ´Â ½ÅüÀû, Á¤½ÅÀûÀÎ ÀÌ»óÀÇ ÃÑĪ. À¯Àü¼º ÁúȯÀ̶ó°íµµ ÇÑ´Ù. º´, ÀÌ»ó ÇüÁúÀÌ À¯ÀüÀû ¿äÀΰú °ü·ÃÀÌ ÀÖÀ½¿¡ µû¶ó¼­ ¹Ýµå½Ã À¯ÀüÀÚ¿¡ ÀÇÇÏÁö ¾Ê´Â À¯ÀüÀûÀÎ º´µµ À¯Àüº´À̶ó°í ÇÏ°Ô µÇ¾ú´Ù. 1°³ÀÇ ¿ì¼º À¯ÀüÀÚ¿¡ ÀÇÇÏ¿© ÀϾ´Â ÇåÆÃÅÏ ¹«µµº´, ¹ß·»ºÎ¸£Å© ÁõÈıº, ¿­¼º À¯ÀüÀÚÀÇ µ¿Çü Á¢ÇÕ¿¡ ÀÇÇÏ¿© ³ªÅ¸³ª´Â ¹éÀÚ, Æä´ÒÄÉÅæ´¢Áõ, X ¿°»öü À§ÀÇ ¹Ý¼º À¯ÀüÀÚ¿¡ ÀÇÇÑ Àû·Ï »ö¸Í, Ç÷¿ìº´, ÁøÇ༺ ±Ù µð½ºÆ®·ÎÇÇÁõ µîÀº ¸í¹éÈ÷ ÀÌÀ¯ ÀüÀÚ¿¡ ÀÇÇÑ °ÍÀ¸·Î¼­, À¯Àüº´ÀÇ ´ëÇ¥ÀûÀÎ °ÍÀ̶ó°í ÇÒ ¼ö ÀÖ´Ù. ¹Ý¼º À¯ÀüÀÚ´Â X ¿°»öü À§¿¡ À§Ä¡ÇÏ´Â °Í¸¸ ¾Ë·ÁÁ® ÀÖ°í, ³²¼ºÀ» °áÁ¤ÇÏ´Â Y ¿°»öü À§¿¡´Â ÇöÀç±îÁö ƯÈ÷ È®½ÇÇÑ ÇüÁúÀ» °áÁ¤ÇÏ´Â À¯ÀüÀÚ´Â Á¸ÀçÇÏÁö ¾Ê´Â´Ù°í º¸°í ÀÖ´Ù. À¯ÀüÀÚ¿¡ ÀÇÇÑ ÀÌ»óÀ̳ª º´Àº Ãâ»ýÇÏ´Â ¾Æ±âÀÇ 1 %°¡ ÀÌ¹Ì °¡Áö°í Àְųª ¹ßº´ÇÒ °¡´É¼ºÀ» Áö´Ï°í ÀÖ´Ù. ¿°»öüÀÇ ±¸Á¶ ¶Ç´Â ±¸¼ºÀÇ ÀÌ»ó¿¡ ÀÇÇÏ¿© ÀϾ´Â ¿©·¯ °¡Áö ÀÌ»ó ´Ù¿î ÁõÈıº, ÅÍ³Ê ÁõÈıº, Ŭ¶óÀÎÆçÅÍ ÁõÈıº µîµµ ¿°»öü À§¿¡ À¯ÀüÀÚ°¡ ÀÖ´Ù°í ÇÏ´Â Àǹ̿¡¼­´Â À¯ÀüÇÐÀûÀÎ °ÍÀ̶ó°í ÇÒ ¼ö ÀÖ´Ù. ±×·¯³ª ´ë°³´Â ÀÌ»ó °³Ã¼¸¦ ¸¸µç ¹è¿ìÀÚ
  • hereditary disturbance
    À¯Àü¼º Àå¾Ö
    ¼±ÃµÀûÀ¸·Î ¾î¹öÀ̷κÎÅÍ ÀÚ¼Õ¿¡°Ô ¹°·ÁÁ® ³»¸®´Â Áúº´.
  • hereditary ectodermal dysplasia
    À¯Àü¼º ¿Ü¹è¿±¼º ÀÌÇü¼ºÁõ
  • hereditary enamel hypoplasia
    À¯Àü¼º ¹ý¶ûÁú ÀúÇü¼ºÁõ
    Ä¡¾Æ ¹ý¶ûÁúÀÇ À¯ÀüÀû ºÒ¿ÏÀü Çü¼º ¶Ç´Â ¹ßÀ° ÀÌ»ó.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
hereditary progressive arthro-ophthalmopathy Autosomal dominant arthro-ophthalmopathy associated with progressive multiple dysplasia of the epiphyses, overtubulation of long bones, cleft lip and palate, hypermobility of joints, flattened vertebral bodies, pelvic bone deformities, and deafness.
Synonym: Stickler's syndrome.
(05 Mar 2000)
adenocarcinoma, mucinous An adenocarcinoma producing mucin in significant amounts.
(12 Dec 1998)
mucinous Relating to or containing mucin.
Synonym: mucoid.
(05 Mar 2000)
mucinous carcinoma <tumour> A variety of adenocarcinoma in which the neoplastic cells secrete conspicuous quantities of mucin, and, as a result, the neoplasms are likely to be glistening, sticky, and gelatinoid in consistency.
Synonym: colloid cancer, colloid carcinoma.
(05 Mar 2000)
mucinous cystic neoplasm of pancreas <radiology> = macrocystic adenoma of pancreas, cystadenoma / cystadenocarcinoma, M:F = 1:9, 40-60 years of age, malignant or pre-malignant, large mass (mean 12 cm), multilocular cysts, thick septations, tail / body in 85% (unlike adenocarcinoma and microcystic adenoma), hypo-/avascular, Differential diagnosis: panc pseudocyst, ** Cf: microcystic adenoma
(12 Dec 1998)
cystadenocarcinoma, mucinous A malignant cystic or semisolid tumour most often occurring in the ovary. Rarely, one is solid. This tumour may develop from a mucinous cystadenoma, or it may be malignant at the onset. The cysts are lined with tall columnar epithelial cells; in others, the epithelium consists of many layers of cells that have lost normal structure entirely. In the more undifferentiated tumours, one may see sheets and nests of tumour cells that have very little resemblance to the parent structure. (hughes, obstetric-gynecologic terminology, 1972, p184)
(12 Dec 1998)
cystadenoma, mucinous A multilocular tumour produced by the epithelial cells of the ovary and having mucin-filled cavities. The great majority of these tumours is benign.
(12 Dec 1998)
neoplasms, cystic, mucinous, and serous Neoplasms containing cyst-like formations or producing mucin or serum.
(12 Dec 1998)
malignant histiocytosis A rapidly fatal form of lymphoma, characterised by fever, jaundice, pancytopenia, and enlargement of the liver, spleen, and lymph nodes; the affected organs show focal necrosis and haemorrhage, with proliferation of histiocytes and phagocytosis of red blood cells.
(05 Mar 2000)
regressing atypical histiocytosis A rare disease characterised clinically by multiple ulcerating cutaneous papules and nodules which show spontaneous regression; the skin is infiltrated by malignant-appearing histiocytes.
(05 Mar 2000)
histiocytosis A condition marked by the abnormal appearance of histiocytes (macrophages) in the blood. Lipid h., Niemann-Pick disease. Sinus h., a disorder of the lymph nodes in which the distended sinuses are completely or nearly completely, filled by histiocytes, as a result of active multiplication of the littoral cells. H. X, a generic term embracing eosinophilic granuloma, Letterer-Siwe disease and Hand-Schuller-Christian disease and indicating a shared common origin for the three entities.
(16 Dec 1997)
histiocytosis, langerhans-cell Group of disorders of histiocyte proliferation which includes letterer-siwe disease, hand-schueller-christian syndrome, and eosinophilic granuloma. Langerhans cells are components of the lesions.
(12 Dec 1998)
histiocytosis, malignant A rare, usually rapidly progressive disorder, characterised by abrupt onset, fever, weight loss, hepato-splenomegaly, pancytopenia, and lymphadenopathy.
(12 Dec 1998)
histiocytosis, non-langerhans-cell Group of disorders which feature accumulations of active histiocytes and lymphocytes, but where the histiocytes are not langerhans cells. The group includes haemophagocytic lymphohistiocytosis, infection-associated haemophagocytic syndrome, sinus histiocytosis, xanthogranuloma, reticulohistiocytoma, juvenile xanthoma, xanthoma disseminatum, as well as the lipid storage diseases (sea-blue histiocyte syndrome and niemann-pick disease).
(12 Dec 1998)
histiocytosis, sinus Benign, non-langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosis with massive lymphadenopathy.
(12 Dec 1998)
ÇÑ¿µ/¿µÇÑ »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • hereditary
    À¯Àü¼ºÀÇ; ¼¼½ÀÀÇ
  • hereditary
    À¯ÀüÀÇ;¼¼½ÀÀÇ;´ë´ëÀÇ
  • hereditary peer
    ¼¼½À ±ÍÁ·
  • progressive
    ÀüÁøÀûÀÎ
  • Progressive Party
    Áøº¸´ç
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