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Dermatologica, 2009
Peutz-Jeghers syndrome is an uncommon genodermatosis. The clinical and radiological features of Peutz-Jeghers syndrome are described in a 12-year-old male child. The relevant literature is briefly reviewed.
B S, Reddy +4 more
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Peutz-Jeghers syndrome is an uncommon genodermatosis. The clinical and radiological features of Peutz-Jeghers syndrome are described in a 12-year-old male child. The relevant literature is briefly reviewed.
B S, Reddy +4 more
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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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Peutz-Jeghers syndrome in a neonate
The Journal of Pediatrics, 1995A 15-day-old girl was found to have generalized gastrointestinal polyposis resulting from Peutz-Jeghers syndrome. Her manifestations included abdominal distention, hematemesis, bloody diarrhea, and edema. She died at 1 year of age of multiple complications of her disease.
M J, Fernandez Seara +5 more
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Cancer in peutz-jeghers syndrome
Cancer, 1993Peutz-Jeghers (P-J) syndrome has been found to be associated with an increased risk of malignant neoplasia.The authors reviewed the clinical courses of eight patients with P-J syndrome (four male and four female patients, ranging in age from 8 to 55 years), who had been followed up for as long as 12 years.
K, Hizawa +6 more
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Peutz-Jeghers syndrome and cancer
Oral Surgery, Oral Medicine, Oral Pathology, 1984A 27-year-old white woman with Peutz-Jeghers syndrome (PJS) associated with a rare but distinctive ovarian tumor, the sex cord tumor with annular tubules (SCTAT), is discussed. Pertinent oral manifestations of PJS and chemotherapy complications are illustrated by the case report.
B, Rodu, M G, Martinez
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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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Intussusception in the Peutz–Jeghers Syndrome
New England Journal of Medicine, 2021Khalid, Akbari, Bruno, Sgromo
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