Results 181 to 190 of about 10,344 (216)
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Dermatologic Clinics, 1995
Peutz-Jeghers syndrome is inherited as an autosomal dominant trait with variable incomplete penetrance. Patients with Peutz-Jeghers syndrome characteristically have hamartomatous polyps throughout their entire gastrointestinal tract, particularly in the small bowel, and mucocutaneous hyperpigmentation involving the lips, oral cavity, and skin. Although
S, Kitagawa, B L, Townsend, A A, Hebert
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Peutz-Jeghers syndrome is inherited as an autosomal dominant trait with variable incomplete penetrance. Patients with Peutz-Jeghers syndrome characteristically have hamartomatous polyps throughout their entire gastrointestinal tract, particularly in the small bowel, and mucocutaneous hyperpigmentation involving the lips, oral cavity, and skin. Although
S, Kitagawa, B L, Townsend, A A, Hebert
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New England Journal of Medicine, 2019
Peutz–Jeghers Syndrome A 45-year-old man presented with abdominal pain and vomiting. He had abdominal tenderness and hyperpigmented macules on the lips, oral mucosa, and nose. Emergency laparotomy revealed jejunojejunal intussusception and multiple polyps. A diagnosis of the Peutz–Jeghers syndrome was made.
Shreya, Sengupta, Sayantan, Bose
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Peutz–Jeghers Syndrome A 45-year-old man presented with abdominal pain and vomiting. He had abdominal tenderness and hyperpigmented macules on the lips, oral mucosa, and nose. Emergency laparotomy revealed jejunojejunal intussusception and multiple polyps. A diagnosis of the Peutz–Jeghers syndrome was made.
Shreya, Sengupta, Sayantan, Bose
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Journal of the American Academy of Dermatology, 2007
Dialogues in Dermatology, a monthly audio program from the American Academy of Dermatology, contains discussions between dermatologists on timely topics. Commentaries from Dialogues Editor-in-Chief Warren R. Heymann, MD, are provided after each discussion as a topic summary and are provided here as a special service to readers of the Journal of the ...
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Dialogues in Dermatology, a monthly audio program from the American Academy of Dermatology, contains discussions between dermatologists on timely topics. Commentaries from Dialogues Editor-in-Chief Warren R. Heymann, MD, are provided after each discussion as a topic summary and are provided here as a special service to readers of the Journal of the ...
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2010
Peutz-Jeghers Syndrome is an autosomal dominant syndrome characterized by hamartomatous gastrointestinal polyps and mucocutaneous melanin pigmentation. Patients are also at risk for extraintestinal neoplasms. In this chapter, the clinicopathologic characteristics of the syndrome, its management and surveillance recommendations will be discussed.
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Peutz-Jeghers Syndrome is an autosomal dominant syndrome characterized by hamartomatous gastrointestinal polyps and mucocutaneous melanin pigmentation. Patients are also at risk for extraintestinal neoplasms. In this chapter, the clinicopathologic characteristics of the syndrome, its management and surveillance recommendations will be discussed.
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JAMA, 1963
ABSTRACT To the Editor: —Recently, in reviewing an issue of The Journal (181:989 [Sept 15] 1962), I was particularly interested in the article by Dr. Harvey Blank of Miami, Fla. He made the statement in regard to Peutz-Jeghers syndrome that not all of the patients have polyps but that polyps should be sought because of the possibility of intestinal ...
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ABSTRACT To the Editor: —Recently, in reviewing an issue of The Journal (181:989 [Sept 15] 1962), I was particularly interested in the article by Dr. Harvey Blank of Miami, Fla. He made the statement in regard to Peutz-Jeghers syndrome that not all of the patients have polyps but that polyps should be sought because of the possibility of intestinal ...
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2014
Peutz-Jeghers syndrome (PJS) is an autosomal dominant polyposis syndrome with high penetrance. It is associated with a germline mutation in the STK11/LKB1 gene (19p13.3) in 80–94 % of patients [1] and has an incidence of about 1 in 8,500 to 1 in 200,000 live births [2–5].
Christopher Fraser, Edward J. Despott
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Peutz-Jeghers syndrome (PJS) is an autosomal dominant polyposis syndrome with high penetrance. It is associated with a germline mutation in the STK11/LKB1 gene (19p13.3) in 80–94 % of patients [1] and has an incidence of about 1 in 8,500 to 1 in 200,000 live births [2–5].
Christopher Fraser, Edward J. Despott
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Peutz–Jeghers Syndrome and the Role of Imaging: Pathophysiology, Diagnosis, and Associated Cancers
Cancers, 2021Ahmed W Moawad, Kamran Ali
exaly
Peutz-Jeghers-Polyp oder Peutz-Jeghers-Syndrom?
Zeitschrift für Gastroenterologie, 2010S Groß +3 more
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