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Èĺ¹¸·°­ÀÇ ÆòÈ°±ÙÀ°Á¾ 1·Ê A Case of Retroperitoneal Leiomyosarcoma

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Abstract

Èĺ¹¸·Á¾¾çÀº 40-50´ë¿¡ È£¹ßÇÏ¸ç ¹ß»ý·üÀº ´ë°³ ¸ðµç ¾Ç¼º Á¾¾çÀÇ 0.2% ÀÌÇÏ·Î º¸°íµÇ
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ÁÖÀ§ Àå±âÀÇ ¾Ð¹Ú°ú ħÀ±À¸·Î ´Ù¾çÇÑ ÀÓ»ó Áõ¼¼°¡ ³ªÅ¸³ª¹Ç·Î Áø´ÜÀÌ ¾î·Æ´Ù. ÀúÀÚµéÀº ¼ú
Àü º¹ÇÕÈ­Çпä¹ý ÈÄ ¼ö¼ú·Î ¿ÏÀü ÀûÃâÀ» ½ÃÇàÇÑ Èĺ¹¸·ÆòÈ° ±ÙÀ°Á¾À» 1·Ê °æÇèÇÏ¿´±â¿¡ ¹®
Çå °íÂû°ú ÇÔ²² º¸°íÇÑ´Ù.

Retroperitoneal tumors are account for fewer than 0.2% of total malignancies.
Retroperitoneal reiomyosarcoma of these are rare and show a tendency toward large size
and extensions by infiltration to the adjacent structure. Thus, the most frequent
symptoms are palpable abdominal mass and abdominal pain. Early detection and
treatment is difficult in retroperitoneal tumor. Aggressive radical surgical excision is
treatment of choice. Modem therapeutic modalilty improve the prognosis, but still
remained debatable prognosis.
We report a case of retroperitoneal leiomyosarcoma in 54-year-old women who was
recieved chemotherapy and then surgical removal.

Å°¿öµå

Retroperitoneum; Leiomyosarcoma;

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KoreaMed
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