Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

¼Ò³ú¡¤¿¬¼ö¡¤Ã´¼ö¸¦ ħ¹üÇÑ ´Ù¹ß¼º Ç÷°ü¸ð¼¼Æ÷Á¾ -1 Áõ·Ê º¸°í- Multiple Hemangioblastomas in Cerebellums Medulla Oblongata and Spinal Cord

´ëÇѺ´¸®ÇÐȸÁö 1995³â 29±Ç 3È£ p.403 ~ 406
ÀÌ¿ø¾Ö, ±è»óÁø, Á¶ÇýÁ¦, °íÀÏÇâ,
¼Ò¼Ó »ó¼¼Á¤º¸
ÀÌ¿ø¾Ö (  ) 
ÀÎÁ¦´ëÇб³ »ó°è¹éº´¿ø Çغκ´¸®°ú

±è»óÁø (  ) 
ÀÎÁ¦´ëÇб³ »ó°è¹éº´¿ø ½Å°æ¿Ü°ú
Á¶ÇýÁ¦ (  ) 
ÀÎÁ¦´ëÇб³ »ó°è¹éº´¿ø Çغκ´¸®°ú
°íÀÏÇâ (  ) 
ÀÎÁ¦´ëÇб³ »ó°è¹éº´¿ø Çغκ´¸®°ú

Abstract

Ç÷°ü¸ð¼¼Æ÷Á¾Àº ¸ðµç µÎ°³³» Á¾¾çÀÇ ¾à 1¡­2%¸¦ Â÷ÁöÇÏ°í, ¼Ò³ú¿¡¼­ °¡Àå ÈçÈ÷ ¹ß»ýÇϸç,
º¸ÅëÀº ´Ü¹ß¼ºÀÌÁö¸¸ ³ú±³, ¿¬¼ö, ô¼ö, ¸Á¸· µî¿¡ ´Ù¹ß¼ºÀ¸·Î ¹ß»ýÇϱ⵵ ÇÑ´Ù. ÀϹÝÀûÀ¸·Î
¼Ò³ú¿¡¼­ ¹ß»ýÇÑ Ç÷°ü¸ð¼¼Æ÷Á¾Àº 'Lindau tumor' ¶ó°í Çϸç, ¸Á¸·¿¡¼­ ¹ß»ýÇÑ °æ¿ì´Â 'von
Hippel tumor' ¶ó°í ºÒ¸°´Ù. ¼Ò³úÀÇ Ç÷°ü¸ð¼¼Æ÷Á¾Àº ¾à 20% Á¤µµ¿¡¼­ ¸Á¸· ¹× ´Ù¸¥ ÁßÃß½Å
°æ°èÀÇ Ç÷°ü¸ð¼¼Æ÷Á¾À̳ª, ½ÅÀå, ÃéÀå, ºÎ½Å, °£, ºñÀå, ºÎ°íȯµîÀÇ ³»ºÎÀå±â¿¡ ºñÁ¾¾ç¼º ³¶ÀÌ
³ª Á¾¾çÀ» µ¿¹ÝÇÑ´Ù. ±¤ÀÇÀÇ von Hippel-Lindau disease¶óÇÔÀº »ó¿°Ã¼¼º ¿ì¼º À¯ÀüÀÇ ´Ù±â
°ü Àå¾Ö·Î¼­ ±âÁ¸ÀÇ °³³ä¿¡¼­ ´õ¿í È®´ëµÇ¾î, ÁßÃ߽Űæ°è³»¿¡ µÎ °³ÀÌ»óÀÇ Ç÷°ü¸ð¼¼Æ÷Á¾ÀÌ
Àְųª, Ç÷°ü¸ð¼¼Æ÷Á¾°ú ´õºÒ¾î ³»ºÎÀå±âÀÇ ³¶¼º ¶Ç´Â Á¾¾ç¼º ÁúȯÀÌ µ¿¹ÝµÇ°Å³ª, °¡Á··ÂÀÌ
ÀÖ´Â °æ¿ì¸¦ ¸ðµÎ Æ÷ÇÔÇÑ´Ù. ±¹³» ¹®Çå¿¡ º¸°íµÈ Ç÷°ü¸ð¼¼Æ÷Á¾Àº ´ëºÎºÐÀÌ ´Ü¹ß¼ºÀÎ °æ¿ìÀÌ
°í, ¹ÚµîÀÌ º¸°íÇÑ 1¿¹¸¸ÀÌ ¼Ò³ú¿¡ ´Ù¹ß¼º Ç÷°ü¸ð¼¼Æ÷Á¾ÀÌ ÀÖÀ¸¸é¼­ ½ÅÀå°ú ÃéÀå¿¡ ³¶¼º º´
º¯ÀÌ µ¿¹ÝµÈ von-Hippel-Lindau disease¿¡ ÇØ´çÇÏ´Â °æ¿ì¿´´Ù. ÀúÀÚµéÀº ¼Ò³ú, °æ¼ö¹× ¿¬¼ö
¿¡ µ¿½Ã¿¡ ¹ß»ýÇÑ ´Ù¹ß¼º Ç÷°ü¸ð¼¼Æ÷Á¾À¸·Î¼­ von Hippel-Lindau disease¿¡ ÇÕ´çÇÑ 1¿¹¸¦
°æÇèÇÏ¿´±â¿¡ ¹®Çå°íÂû°ú ÇÔ²² º¸°íÇÏ´Â ¹ÙÀÌ´Ù.
#ÃÊ·Ï#
Hemangioblastomas comprise 1 to 2% of all intracranial neoplasm, and 8 to 12% of
tumors within the posterior fossa. They are composed of admixtures of three different
cell types; endothelial cells, pericytes and stromal cells. Although most
hemangioblastomas arise sporadically, they are associated with von Hippel-Lindau
disease in about 20% cases. We have experienced a case of multiple hemangioblastomas
occuring in the cerebellum, medulla oblongata and cervical spinal cord simultaneously in
a 55-year-old male. He had complained of headache, dizziness, generalized weariless and
gait disturbance for 2 weeks. The patient had neither specific family history nor
increased hematocrit. MRI showed a nonenhancing cystic lesion with an enhancing mural
nodule in the right cerebellar hemisphere and two separate enhancing nodules in the
medulla oblongata and dorsal cervical spinal cord at the 5-6th. Grossly, the excised
mass of the cerebellum, 2.5¡¿2¡¿1.8 §¯, was solid to partly cystic, and that of spinal
cord, 1cm in diameter, was mostly solid. Microscopically, the tumor was composed of
thin-walled blood vessels in variable size and interspersed stromal cells. The stromal
cells revealed dimorphic cytoplasm that were either homogeneous and eosinophilic, or
clear and vacuolated. Immunohistochemically, the endothelial cells reacted positively for
glial fibrillary acidic protein(GFAP) and vimentin. The stromal cells reacted diffusely
positively for vimentin, focally positively for GFAP and S-100 protein near the periphery
of the tumor, focally positively for neuron specipic enolase(NSE), and negatively for
lysozyme, desmin and chromogranin. Ultrastructurally, the stromal cells contained
numerous microfilaments and lipid droplets.

Å°¿öµå

Multiple hemangioblastomas; Cerebellum; Medulla oblongata; Spinal cord; Von Hippel-Lindau disease;

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

   

µîÀçÀú³Î Á¤º¸

KCI
KoreaMed
KAMS