Peutz-Jeghers syndrome is an autonomic dominant disease characterized by hamartomatous polyps and mucocutaneous hyperpigmentation. We present 16 cases; females were more affected. The most common presenting complaints were of gastrointestinal tract. All polyps found were hamartomatous with general distribution through gastrointestinal tract. Endoscopic
Roberto, Cervantes Bustamante +6 more
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Severe Iron Deficiency Anemia in a Jehovah's Witness diagnosed with Peutz-Jeghers Syndrome. [PDF]
Gulla V +5 more
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Adrenocortical Carcinoma in Peutz-Jeghers Syndrome With a Rare STK11 Pathogenic Germline Variant: A Case Report. [PDF]
Ishida T +14 more
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Peutz -Jeghers syndrome (PJS) [PDF]
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Familial pediatric Peutz-Jeghers syndrome with recurrent intussusception: case report and literature review. [PDF]
Sahli S +7 more
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Gastric-type endocervical adenocarcinoma with Peutz-Jeghers syndrome: a case report and literature review. [PDF]
Li J, Lu R, Lin H, Sun D, Fan J.
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Mutation profile and therapeutic implications in Peutz-Jeghers syndrome-associated gastric-type endocervical adenocarcinoma. [PDF]
Niu T +5 more
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Acute intestinal intussusception revealing Peutz-Jeghers Syndrome in a 16-year-old male: a case report. [PDF]
Atri S +5 more
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Neurofibromatosis type 1 with concomitant Peutz-Jeghers syndrome in a child: a case report. [PDF]
Liu Q, Long Y.
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Peutz-Jeghers syndrome with concurrent lobular endocervical glandular hyperplasia and sex cord tumor with annular tubules: a case report. [PDF]
Yin M, Lu C, Cheng L.
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