Blog - INTERNET MÉDICA

Síndrome de Heyde II (Heyde´s Syndrome II)

Por Paulo Leite 23/05/2023

– A síndrome de Heyde é uma tríade de angiodisplasia colônica hemorrágica, estenose aórtica e coagulopatia adquirida. É mais comumente visto em idosos entre 60-80 anos de idade. A principal hipótese que explica a etiologia desta síndrome é a doença de von Willebrand adquirida, mas nem todos os estudos apóiam essa afirmação. A síndrome de Heyde é descrita em 1,7% dos pacientes com estenose aórtica importante. A indicação de intervenção valvar nesses pacientes segue as diretrizes atuais e, apesar de não existirem recomendações específicas, alguns centros defendem intervenção para redução de sangramento independente da presença de sintomas ou complicadores

■ Heyde´s syndrome: a systematic review of case reports

Bibek Saha, Eric Wien, Nicholas Fancher, et al

BMJ Open Gastroenterol. 2022; 9(1): e000866

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086603/

■ Síndrome de Heyde: estratégias terapêuticas e seguimento de longo prazo

V E E Rosa, F Tarasoutchi

Arq Bras Cardiol 2021, vol 117 (3)

https://www.scielo.br/j/abc/a/yxGGvG5hZZJWyG7dvMj3Jxq/

■ Multimodal treatment and diangostic modalities in the setting of Heyde´s syndrome: a systematic review

Dawood Jamil, Hadrian Hoang-Vu Tran, Mafaz Mansoor et al

Cureus. 2022 Aug; 14(8): e28080.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9477546/

■ Aortic stenosis and Heyde´s syndrome: a comprehensive review

Dennisdhilak Lourdusamy, Vamsee Krishna Mupparaju, Navila Fahmida Sharif, Uzoma N Ibebuogu

World J Clin Cases. 2021 Sep 6; 9(25): 7319–7329

■ Heyde syndrome treated by conventional aoritc valve replacement

A M Farzesi, G Tripoli, N L K L de Campos et al

Braz J Cardiovasc Surg 2019, vol 34 (5)

https://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-76382019000500630

■ Aortic stenosis and Heyde´s syndrome: a comprehensive review

Dennisdhilak Lourdusamy, Vamsee Krishna Mupparaju, Navila Fahmida Sharif, Uzoma N Ibebuogu

World J Clin Cases. 2021 Sep 6; 9(25): 7319–7329

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8464459/

■ Heyde syndrome: prevalence and outcomes in patients undergoing transcatheter aortic valve implantation

Lara Waldschmidt, Andreas Drolz, Paula Heimburg, et al

Clin Res Cardiol. 2021; 110(12): 1939–1946

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639542/

■ New onset Heyde´s syndrome presenting after total aortic valve replacement

Eric Omar Then, Carmine Catalano, Tagore Sunkara, Vinaya Gaduputi

Oxf Med Case Reports. 2019 Feb; 2019(2): omy134

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380530/

■ Recurrent gastrointestinal bleeding in a patient with severe aortic valve stenosis: a diagnosis of Heyde´s syndrome

Adham E Obeidat, Jean Kim

Cureus. 2021 Jun; 13(6): e1544

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8255048/

■ Recurrent gastrointestinal bleeding in a patient with Heyde syndrome with elevated fator VIII levesl: a case report

Omar Al-Radaideh, Iyad Farouji, Hossam Abed, Hamid Shaaban

Int J Crit Illn Inj Sci. 2021 Oct-Dec; 11(4): 253–256

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8725811/

■ Medical management of Heyde syndrome

Samridhi Sinha, Daniel Castro, Shams Shakil

Cureus. 2021 Jan; 13(1): e12551

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7863051/

■ Síndrome de Heyde I (Heyde´s Syndrome I)

Arquivos Blog Internet Médica – fevereiro 2018

https://internetmedica.com.br/sindrome-de-heyde-online-heydes-syndrome/

■ Acesso gratuito

■ Um dos Blog de Medicina mais acessado em todo o mundo. Mais de 900 temas médicos já disponíveis online

■ Use o mecanismo de busca – PESQUISAR na home page.

■ Acesse ARQUIVO e encontre os temas incluídos no Blog a cada mês, desde maio 2017

■ Blog Internet Médica – www.internetmedica.com.br

■ Médico Responsável: Dr Paulo Fernando Leite

CRMMG: 7026

Belo Horizonte/MG/Brasil

Email: pfleite1873@gmail.com

Maio 2023

Genética Médica: Artigos de Revisão/Diretrizes Médicas (Medical Genetics: Review Articles/Guidelines)

Por Paulo Leite 19/05/2023

■ Hereditary cancer syndromes

E N Imyanitov, E S Klligina, A P Sokolenko et al

World J Clin Oncol 2023, vol 14 (2): 40-68

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993141/

■ Genetic predisposition to colorectal cancer: How many and whic gene to test?

Francesca Rebuzzi, Paola Ulivi, Gianluca Tedaldi

Int J Mol Sci. 2023 Feb; 24(3): 213

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9916931/

■ Genetics, genomics and emerging molecular therapies of pancreatic cancer

Jakub Liu, Magdalena Mroczek, Anna Mach et al

Cancers (Basel) 2023 Feb; 15(3): 77

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9913594/

■ Genetic counselling and testing in pulmonar arterial hypertension: a consensus statement on behalf of the International Consortium for genetic studies in PAH

Christina A. Eichstaedt, Catharina Belge, Wendy K. Chung

Eur Respir J. 2023 Feb; 61(2): 220147

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947314/

■ Practice guidelines for BRCA1/2 tumour testing in ovarian cancer

Daria Grafodatskaya, Darren D O’Rielly, Karine Bedard et al

J Med Genet. 2022 Aug; 59(8): 727–736

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340048/

■ UK consensus recommendations for clinical management of cancer risk for women with germline pathogenic variantes in cancer predisposition genes: RAD51C,_RAD51D_BRIP1 and PAlB2

Helen Hanson, Anjana Kulkarni, Lucy Loong et al

On behalf of Consensus meeting attendees, Fiona Lalloo

J Med Genet. 2023 May; 60(5): 417–429

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10176381/

■ Automated clinical practice guideline recommendations for hereditary cancer risk using chatbots and ontologies: systemm description

Jordon B Ritchie, Lewis J Frey, Jean-Baptiste Lamy, et al

JMIR Cancer. 2022 Jan-Mar; 8(1): e29289

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845001/

■ The international WAO/EAACI guideline for the management of hereditary angioedema – The 2021 revision and update

Marcus Maurer, Markus Magerl, Stephen Betschel et al

World Allergy Organ J. 2022 Mar; 15(3): 100627

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023902/

■ Brazilian consensus for diagnosis, management and treatment of hereditary tansthyretin amyloidosis with peripheral neuropahy: second edition

Marcus Vinicius Pinto, Marcondes Cavalcante França, Jr, Marcus Vinicius Magno Gonçalves et al

Arq Neuropsiquiatr. 2023 Mar; 81(3): 308–321

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104762/

■ Clinical guidelnes for diagnosis and management of juvenile polyposis syndrome in children and adults – secondary publication

Takayuki Matsumoto, Junji Umeno, Keisuke Jimbo, et al

J Anus Rectum Colon. 2023; 7(2): 115–125

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10129355/

■ Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement

F Brioude, J M Kalish, A Mussa et al

Nat Rev Endocrinol 2018, vol 14 (4): 229-249

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022848/