- Hereditary Hemorrhagic Telangiectasia in a Family
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Park HW, Chun SI
- KMID: 1920712
- Korean J Dermatol.
- 1990 Dec;28(6):826-830.
We report three cases of hereditary hemorrhagic telangiectasia in one family. The punctiform, spider-like and nodular telangieectatic lesions were presented in these all patients, the father, son an daughter. But... -
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- Hereditary Hemorrhagic Telangiectasia Combined with Pulmonary Arteriovenous Malformation Treated with Transcatheter Embolotherapy
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Park YW, Yeom KB, Kim KH
- KMID: 2301604
- Korean J Dermatol.
- 2012 Aug;50(8):752-754.
No abstract available. -
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- A Case of Hereditary Hemorrhagic Telangiectasia
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Chang DS, Kim MN, Hong CK, Ro BI
- KMID: 2303102
- Korean J Dermatol.
- 2002 Sep;40(9):1148-1150.
Hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber disease, is an autosomal dominant hereditary disorder leading to easily bleeding telangiectases on skin and mucosal surfaces, and it is associated with the... -
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- Genetic Mutation Analysis Can Supplement Clinically Confirmed Hereditary Hemorrhagic Telangiectasia Populations
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Kim ST
- KMID: 2462727
- Clin Exp Otorhinolaryngol.
- 2019 Nov;12(4):333-334.
- doi: 10.21053/ceo.2019.01585
No abstract available. -
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- Hepatic Involvement in Hereditary Hemorrhagic Telangiectasia
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Han JK, Kim SH
- KMID: 760570
- Korean J Hepatol.
- 2004 Dec;10(4):322-324.
No abstract available. -
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- A Case of Hepatic Involvement in Hereditary Hemorrhagic Telangiectasia Presenting as High Output Heart Failure
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Min JS, Park HY, Park JI, Park SR, Moon J, Lee SB
- KMID: 2224189
- Keimyung Med J.
- 2015 Dec;34(2):204-208.
- doi: 10.0000/kmj.2015.34.2.204
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease, is a rare autosomal dominant vascular disorder involving arteriovenous malformation. HHT is characterized by recurrent epistaxis, cutaneous telangiectasia, and visceral arteriovenous... -
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- A Case of Hereditary Hemorrhagic Telangiectasia
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Park HJ, Eun HC, Lee YS
- KMID: 1678743
- Korean J Dermatol.
- 1983 Aug;21(4):415-419.
Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) is a familial disease that is characterized by delicate, ectatic vessels in the skin, mucous membrane and viscera. These patients have a generalized vascular derangement... -
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- Hereditary Hemorrhagic Telangiectasia with Pulmonary Arteriovenous Fistula
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Kim HJ, Yoon YS, Seo JK, Moon HR, Yeon KM
- KMID: 1698924
- J Korean Pediatr Soc.
- 1984 Apr;27(4):390-394.
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- A Case of Hereditary Hemorrhagic Telangiectasia Combined with Pulmonary- Systemic Fistula
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Chang SA, Oh S, Koo JM, Kim HK, Cho HJ, Park SR, Lee MM, Park YB, Choi YS
- KMID: 2029616
- Korean Circ J.
- 2003 Feb;33(2):139-142.
- doi: 10.4070/kcj.2003.33.2.139
We report the first case of hereditary hemorrhagic telangiectasia combined with multiple pulmonary-systemic fistulae. In this case, a 39-year-old woman presented with long standing chest pain, dyspnea and hemoptysis. Finally... -
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- Two Cases of High Output Heart Failure Caused by Hereditary Hemorrhagic Telangiectasia
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Cho D, Kim S, Kim M, Seo YH, Kim W, Kang SH, Park SM, Shim W
- KMID: 1491105
- Korean Circ J.
- 2012 Dec;42(12):861-865.
- doi: 10.4070/kcj.2012.42.12.861
High-output cardiac failure is a rare complication of hereditary hemorrhagic telangiectasia (HHT) usually caused by shunting of blood through atriovenous malformations (AVMs) in the liver. We describe two cases of... -
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- A Case of Hereditary Hemorrhagic Telangiectasia
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Kim DH, Kim KH, Hahn JS
- KMID: 2251037
- Korean J Dermatol.
- 2001 Sep;39(9):1048-1050.
Hereditary hemorrhagic telangiecatasia(HHT) is a familial syndrome inherited by an autosomal dominant mode and characterized by recurrent epistaxis with multiple telangiectatic lesions on the mucosa and skin. Recently we experienced... -
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- A case of hereditary hemorrhagic telangiectasia
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Lee YS, Kim S, Kang EK, Park JD
- KMID: 2279317
- Korean J Pediatr.
- 2007 Oct;50(10):1018-1023.
- doi: 10.3345/kjp.2007.50.10.1018
Hereditary hemorrhagic telagiectasia (HHT), which is characterized by the classic triad of mucocutaneous telangiectases, arteriovenous malformations (AVMs) and inheritance, is an autosomal dominant disorder. The characteristic manifestations of HHT are... -
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- Splenic Arteriovenous Malformation Manifestated by Thrombocytopenia in Hereditary Hemorrhagic Telangiectasia: A Case Report
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Kwon HJ, Choi JC, Oh JY, Cho JH, Kang M, Lee JH, Yoon SK, Nam KJ
- KMID: 2103918
- J Korean Radiol Soc.
- 2008 Sep;59(3):197-200.
- doi: 10.3348/jkrs.2008.59.3.197
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant inherited disease characterized by epistaxis, telangiectases and visceral arteriovenous malformations (AVMs). The involvement of the gastrointestinal tract, liver, lung and cerebrum for... -
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- Mucocutaneous Telangiectasia as a Diagnostic Clue of Hereditary Hemorrhagic Telangiectasia: An Activin Receptor-Like Kinase-1 Mutation in a Korean Patient
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Seo J, Chu H, Lee JS, Kim DY
- KMID: 2171394
- Ann Dermatol.
- 2016 Apr;28(2):264-266.
- doi: 10.5021/ad.2016.28.2.264
No abstract available. -
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- A Case of Hereditary Hemorrhagic Telangiectasia Managed with Intranasal Topical Estrogen
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Song JW, Kim HJ, Yoon YR, Kim YT
- KMID: 2276630
- Korean J Otolaryngol-Head Neck Surg.
- 2006 Apr;49(4):447-450.
Hereditary hemorrhagic telangiectasia is an autosomal dominant disorder affecting blood vessels of the skin, mucous membrane and viscera. It is characterized by a clinical triad of multiple telangiectasia, recurrent hemorrhages... -
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- ST Elevation Myocardial Infarction in a Patient with Hereditary Hemorrhagic Telangiectasia Involving the Liver
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Kim SK, Lee SH, Kim K, Kim BI
- KMID: 2382659
- Korean J Med.
- 2017 Apr;92(2):182-185.
- doi: 10.3904/kjm.2017.92.2.182
This is a case report of a 71-year-old woman with hereditary hemorrhagic telangiectasia (hereditary hemorrhagic telangiectasia [HHT], Osler–Weber–Rendu syndrome) involving the liver who developed ST elevation myocardial infarction and died... -
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- Usefulness of Septodermoplasty in Hereditary Hemorrhagic Telangiectasia
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Yang CJ, Lee BJ, Jang YJ
- KMID: 2277862
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2015 May;58(5):330-336.
- doi: 10.3342/kjorl-hns.2015.58.5.330
BACKGROUND AND OBJECTIVES: Epistaxis is the most common symptom in patients with hereditary hemorrhagic telangiectasia (HHT). The aim of this study is to report treatment of severe epistaxis related to... -
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- A Case of Hereditary Hemorrhagic Telangiectasia
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Lee HE, Sagong C, Yeo KY, Ko JY, Kim JS, Yu HJ
- KMID: 2219399
- Ann Dermatol.
- 2009 May;21(2):206-208.
- doi: 10.5021/ad.2009.21.2.206
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... -
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- Three Cases of Hereditary Hemorrhagic Telangiectasia Treated with Bevacizumab
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Lee M, Park P, Kim D, Jin HR
- KMID: 2350486
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2016 Aug;59(8):613-619.
- doi: 10.3342/kjorl-hns.2016.59.8.613
Hereditary hemorrhagic telangiectasia (HHT) is a hereditary, autosomal dominant, vascular dysplasia characterized by mucocutaneous telangiectasia, epistaxis, gastrointestinal bleeding, and iron deficiency anemia. Epistaxis in HHT is a recurrent and debilitating... -
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- Posterior Cerebral Artery Infarction in a Patient with Coexisting Hereditary Hemorrhagic Telangiectasia and Patent Foramen Ovale
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Lee HS, Lee EJ, Kim R, Jun JS, Lee WJ, Lee YS
- KMID: 2184611
- J Korean Neurol Assoc.
- 2015 Aug;33(3):217-220.
- doi: 10.17340/jkna.2015.3.16
Patients with hereditary hemorrhagic telangiectasia (HHT) are at risk of developing pulmonary arteriovenous malformations (pAVMs). Paradoxical embolism may occur through pAVMs or patent foramen ovale (PFO) and lead to cerebral... -
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