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Mucosal prolapse syndrome mimicking Peutz-Jeghers syndrome in a pediatric patient. [PDF]
JPGN RepDo P +4 more
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Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome. [PDF]
Turk J GastroenterolAslan PG +8 more
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Peutz-Jeghers Syndrome: A Comprehensive Review of Genetics, Clinical Features, and Management Approaches. [PDF]
CureusAmru RL, Dhok A.
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Ischemic Polypectomy Through Detachable Snare and Rubber Band Ligation in Peutz-Jeghers Syndrome. [PDF]
ACG Case Rep JTan JRL, Co JT.
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Poorly differentiated adenocarcinoma of the jejunum in a patient with Peutz-Jeghers syndrome: A case report. [PDF]
Int J Surg Case RepMiresa F +4 more
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Global research landscape of Peutz-Jeghers syndrome and successful endoscopic management of intestinal intussusception in patients with recurrent laparotomies. [PDF]
World J Gastrointest SurgSun Q +7 more
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JAMA Dermatology, 2022
This case report describes multiple dark-brown 1- to 2-mm hyperpigmented macules on the lips, nose, and conjunctivae.
Eri, Sato, Takao, Goto, Hitoshi, Honda
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This case report describes multiple dark-brown 1- to 2-mm hyperpigmented macules on the lips, nose, and conjunctivae.
Eri, Sato, Takao, Goto, Hitoshi, Honda
openaire +2 more sources
Current Opinion in Gastroenterology, 2021
Purpose of review Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 (STK11/LKB1) genes.
Ilja, Tacheci +2 more
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Purpose of review Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 (STK11/LKB1) genes.
Ilja, Tacheci +2 more
openaire +2 more sources
Australian and New Zealand Journal of Surgery, 1985
Peutz‐Jeghers syndrome has now been widely reported. A case with previously unrecorded conjunctival pigmentation is presented and the management is reviewed.
P A, Dewan, J K, Hope
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Peutz‐Jeghers syndrome has now been widely reported. A case with previously unrecorded conjunctival pigmentation is presented and the management is reviewed.
P A, Dewan, J K, Hope
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The American Journal of Gastroenterology, 2000
Peutz-Jeghers syndrome (PJS) is an unusual polyposis syndrome that has enjoyed a rich and somewhat confusing history. Mucocutaneous pigmentation and diffuse gastrointestinal hamartomas are the hallmark features of this autosomal dominant inherited condition. Peutz-Jeghers syndrome is now also recognized as a cancer predisposition syndrome.
T J, McGarrity, H E, Kulin, R J, Zaino
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Peutz-Jeghers syndrome (PJS) is an unusual polyposis syndrome that has enjoyed a rich and somewhat confusing history. Mucocutaneous pigmentation and diffuse gastrointestinal hamartomas are the hallmark features of this autosomal dominant inherited condition. Peutz-Jeghers syndrome is now also recognized as a cancer predisposition syndrome.
T J, McGarrity, H E, Kulin, R J, Zaino
openaire +4 more sources