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Peutz-Jeghers Syndrome

New Approach Pits Old Drug Against Troublesome Pathway
New Approach Pits Old Drug Against Troublesome Pathway administrator 1 Views • 2 years ago

Duncan Family Institute seed grant helps Chongjuan Wei test medication in her mouse model of Peutz-Jeghers syndrome, aiming at a molecular chain active in many cancers. More information:
http://www.mdanderson.org/educ....ation-and-research/d

Peutz Jeghers syndrome
Peutz Jeghers syndrome administrator 1 Views • 2 years ago

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Peutz Jeghers Syndrome Hamartomas of the stomach - Todua Clinic
Peutz Jeghers Syndrome Hamartomas of the stomach - Todua Clinic administrator 1 Views • 2 years ago

PEUTZ JEGHERS SYNDROME
PEUTZ JEGHERS SYNDROME administrator 1 Views • 2 years ago

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Colonic polyps
Colonic polyps administrator 2 Views • 2 years ago

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Síndrome de Peutz-Jeghers
Síndrome de Peutz-Jeghers administrator 2 Views • 2 years ago

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2162093
2162093 administrator 2 Views • 2 years ago

Combined Surgical and Endocospic Management of Recurrent Intussusception Secondary to Peutz-Jeghers Syndrome
Endoscopic ischemic polypectomy for small-bowel polyps in patients with Peutz–Jeghers syndrome
Endoscopic ischemic polypectomy for small-bowel polyps in patients with Peutz–Jeghers syndrome administrator 1 Views • 2 years ago

Endoscopic ischemic polypectomy for small-bowel polyps in patients with Peutz–Jeghers syndrome

Authors: Tsevelnorov Khurelbaatar, Hirotsugu Sakamoto, Tomonori Yano et al.

Summary:
Retrospective analysis showing effectiveness and safety of ischemic polypectomy in 352 polyps larger than 5mm during repeated double-balloon enteroscopy in Japanese patients with Peutz–Jeghers syndrome. A decreasing trend in polypectomies of polyps larger than 15mm was seen over time.

Bibliography
Endoscopy 2021; 53: 744–748
DOI 10.1055/a-1276-6452
ISSN 0013-726X
© 2020. Thieme. All rights reserved.
Georg Thieme Verlag KG, Rüdigerstraße 14,
70469 Stuttgart, Germany

Read more here: https://doi.org/10.1055/a-1276-6452

Síndrome de Peutz Jeghers
Síndrome de Peutz Jeghers administrator 2 Views • 2 years ago

A síndrome de Peutz-Jeghers (SPJ) é uma condição hereditária autossômica dominante rara, caracterizada pela presença de múltiplos pólipos hamartomatosos no estômago, intestino delgado e colo, acompanhada de lesões epidérmicas pigmentadas distintivas.
O seu surgimento se dá pela herança de uma mutação no gene STK11, também chamado de LKB1. Alguns pesquisadores consideram que possam existir outros genes causadores SPJ que ainda não foram estudados.

Sem o acompanhamento de um especialista, o risco do desenvolvimento de câncer ao longo da vida em pessoas com a doença pode chegar a 93%.
Indivíduos com pelo menos 2 das seguintes características podem ser considerados portadores de SPJ:
Pelo menos 2 pólipos hamartomatosos do tipo Peutz-Jeghers no intestino delgado
Sardas características da boca, lábios, dedos das mãos ou pés
Pelo menos 1 parente diagnosticado com SPJ
Recomenda-se que os indivíduos que atendem a esses critérios façam testes genéticos para rastreio de mutação herdada, também chamada de alteração, no gene STK11
#draandrezasouto #oncologia #oncogenetica #oncologiaclinica #oncologistaembrasilia #oncoclinicas #shorts
Peutz–Jeghers syndrome (Medical Condition)
Peutz–Jeghers syndrome (Medical Condition) administrator 2 Views • 2 years ago

Symptoms, risk factors and treatments of Peutz–Jeghers syndrome (Medical Condition)

Peutz-Jeghers syndrome, also known as hereditary intestinal polyposis syndrome, is an autosomal dominant genetic disease characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa

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Music: 'Undaunted' Kevin Macleod CC-BY-3.0
Source/Images: "Peutz–Jeghers syndrome" CC-BY-2.5 https://www.freebase.com/m/048vkz

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