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A Case of Recurrent Abdominal Pain with Fever and Urticarial Eruption
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ÀÌâ±Ù(Lee Chang-Geun) - µ¿±¹´ëÇб³ Àϻ꺴¿ø ³»°ú
ÀÓÀ±Á¤(Lim Yun-Jeong) - µ¿±¹´ëÇб³ Àϻ꺴¿ø ³»°ú
°Çö¿ì(Kang Hyoun-Woo) - µ¿±¹´ëÇб³ Àϻ꺴¿ø ³»°ú
±èÀçÇÐ(Kim Jae-Hak) - µ¿±¹´ëÇб³ Àϻ꺴¿ø ³»°ú
ÀÌÁرÔ(Lee Jun-Kyu) - µ¿±¹´ëÇб³ Àϻ꺴¿ø ³»°ú
°í¹®¼ö(Koh Moon-Soo) - µ¿±¹´ëÇб³ Àϻ꺴¿ø ³»°ú
ÀÌÁøÈ£(Lee Jin-Ho) - µ¿±¹´ëÇб³ Àϻ꺴¿ø ³»°ú
ÇãÈñÁø(Huh Hee-Jin) - µ¿±¹´ëÇб³ Àϻ꺴¿ø Áø´Ü°Ë»çÀÇÇаú
À̽ÂÈ£(Lee Seung-Ho) - µ¿±¹´ëÇб³ ÀÇ°ú´ëÇÐ Àϻ꺴¿ø ÇǺΰú
Abstract
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent episodes of fever and serosal, synovial, or cutaneous inflammation, caused by a dysfunction of pyrin as a result of mutation within the MEFV gene. It occurs mainly among Mediterranean and Middle Eastern populations, including Jews, Arabs, and Turks. However, FMF cases have been reported outside the Mediterranean and Middle Eastern countries in recent years. Although FMF has been relatively rare in Korea until now, proper recognition of FMF might lead to more frequent diagnoses of FMF. We experienced an interesting case, a 31-year-old Korean man who presented with recurrent abdominal pain with fever and urticarial eruption for 10 years. DNA analysis showed complex mutations (p.Leu110Pro, p.Glu148Gln) in the MEFV gene. To date, three cases have been reported, and this case of FMF with skin conditions is the first case in Korea.
Å°¿öµå
Familial Mediterranean fever, Abdominal pain, Urticaria
KMID :
0614620140640010040
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