지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2009.1
- 수록면
- 206 - 208 (3page)
이용수
초록· 키워드
오류제보하기
Hereditary hemorrhagic telangiectasia, also known as
Osler-Weber-Rendu disease, is an autosomal dominant disorder
of the fibrovascular tissue. It is characterized by the
classic triad of mucocutaneous telangiectasias, recurrent
hemorrhages, and familial occurrence. The cutaneous manifestation
appear clinically as punctuate, linear, or splinter-
like telangiectasias of the upper body, oral, and nasal mucous
membranes, and nail beds. A 73-year-old woman presented
with purpuric, punctuate, and tiny macules on the finger
tips of both hands and the tongue. The skin lesions were
discovered about 50 years previously. She had a family history
of cutaneous telangiectasia. Also, she had episodes of recurrent
epistaxis, gastrointestinal bleeding, and anemia. The
gastroendoscopy revealed gastric angiodysplasia of the fundus
and body of the stomach. The histopathologic study
showed dilated capillaries lined by flat endothelial cells in
the papillary dermis. From these findings, we diagnosed this
case as hereditary hemorrhagic telangiectasia, which has
rarely been reported in the dermatologic literature.
목차
등록된 정보가 없습니다.
참고문헌 (8)
참고문헌 신청
Abdalla SA / 2006 / Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease / J Med Genet 43 : 97 ~ 110
Bossler AD / 2006 / Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia
Fernandez-Jorge B / 2007 / Treatment of cutaneous and mucosal telangiectases in hereditary hemorrhagic telangiectasia: report of three cases / J Cosmet Laser Ther 9 : 29 ~ 33
Garzon MC / 2007 / Vascular malformations. Part II: associated syndromes / J Am Acad Dermatol 56 : 541 ~ 564
Juares AJ / 2008 / Rendu-Osler-Weber Syndrome: case report and literature review / Braz J Otorhinolaryngol 74 : 452 ~ 457
Bossler AD / 2006 / Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia
Fernandez-Jorge B / 2007 / Treatment of cutaneous and mucosal telangiectases in hereditary hemorrhagic telangiectasia: report of three cases / J Cosmet Laser Ther 9 : 29 ~ 33
Garzon MC / 2007 / Vascular malformations. Part II: associated syndromes / J Am Acad Dermatol 56 : 541 ~ 564
Juares AJ / 2008 / Rendu-Osler-Weber Syndrome: case report and literature review / Braz J Otorhinolaryngol 74 : 452 ~ 457
함께 읽어보면 좋을 논문
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