본문 바로가기
KERD
논문KCI 등재

유전성 비용종성 대장직장암에 동반된자궁내막암 1예

A Case of Endometrial Cancer with Hereditary Non-Polyposis Colorectal Cancer (HNPCC)

0

조회

0

다운로드

1

인용

0

참고문헌

키워드

주제분류산부인과학

초록

자궁내막암은 유전성 비용종성 대장직장암과 동반될 수 있는 가장 흔한 악성 질환이며 Lynch II 증후군으로 알려진 유전성 비용종성 대장직장암은 다른 장기, 특히 자궁내막에 암을 유발할 수 있는 상염색체 우성의 유전방식으로 유전되는 대장용종 질환이다. 유전성 비용종성 대장암 여성 환자에 있어서 자궁내막암의 평생위험률은 일반 여성의 3%의 비해 40- 60%로 높은 비율을 보인다. 이러한 자궁내막암의 평균 발생연령은 45세이고 종종 대장암보다 먼저 발병할 수 있다. 저자들은 최근 새롭게 발생한 유전성 비용종성 대장직장암 (de novo type of hereditary non-polyposis colorectal cancer)과 동반된 자궁내막암 1예를 경험하였기에 문헌 고찰과 함께 보고하는 바이다. ‘

Abstract

Endometrial cancer is the most common malignant disorder that can be associated with hereditary non-polyposis colorectal cancer (HNPCC), which is known as Lynch II syndrome. HNPCC is a polyposis of the colon which is inherited in an autosomal dominant pattern and can cause cancer in other organs, especially in the endometrium. The overall risk of a women with HNPCC to develop endometrial cancer is 40-60%, much higher than the 3% of the general population of women. The average age of developing endometrial cancer of a women with HNPCC is 45 years of age and is often found before development of colon cancer. We have recently experienced a case of de novo type of hereditary non-polyposis colorectal cancer associated with endometrial cancer, hence we are reporting this case with a brief review of literatures.

참고문헌 (17)

  1. Watson P, "Colorectal carcinoma survival among hereditary nonpolyposis colorectal carcinoma family members", 83, pp.259~66 (1998)
  2. Peinado MA, "Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis", io(v y), pp.558~61 (1993)
  3. Baba S, "New strategies for treatment of hereditary colorectal cancer" (1996)
  4. Aarnio M, "Cancer risk in mutation carriers of DNA-mismatch-repair genes", 81(2), pp.214~8 (1999)
  5. Banno K, "Association of HNPCC and endometrial cancers", 9(4), pp.262~9 (2004)
  6. Umar A, "Testing guidelines of heretary non-polyposis colorectal cancer", 4, pp.153~8 (2004)
  7. Raut CP, "Clinicopathologic features in colorectal cancer patients with microsatellite instability", 568(2), pp.275~82 (2004)
  8. Muller A, "Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry", 6(4), pp.308~15 (2004)
  9. Boland CR, "National Cancer Institute workshop on microsatellite instability in colorectal cancer", 58, pp.5248~57 (1998)
  10. Pedroni M, "Microsatellite instability in multiple colorectal tumors", 81, pp.1~5 (1999)
  11. Samowitz WS, "Microsatellite instability in sporadic colon cancer is associated with an improved prognosis at the population level", 10(9), pp.917~23 (2001)
  12. Gryfe R, "Tumor microsatellite instability and clinical outcome in young patients with colorectal cancer", 342(2), pp.69~77 (2000)
  13. Bonner JD, "Phenotype of microsatellite unstable colorectal carcinomas well- differentiated and focally mucinous tumors and the absence of dirty necrosis correlate with microsatellite instability", 27(5), pp.563~70 (2003)
  14. Young J, "Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings", 159(6), pp.2107~16 (2001)
  15. Watson PV, "The risk of endometrial cancer in hereditary nonpolyposis colorectal cancer", 96, pp.516~20 (1994)
  16. Watson P, "The tumor spectrum in HNPCC", 14, pp.1653~4 (1994)
  17. Tomita N, "The novel germline mutation of the hMLH1 gene in a case of suspected hereditary non-polyposis colorectal cancer in a patient with no family history of cancer", 34(9), pp.556~60 (2004)

관련 논문AI추천

이 간행물의 다른 논문 (18건)