"Peutz-Jeghers Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.
| Descriptor ID |
D010580
|
| MeSH Number(s) |
C04.700.705 C06.405.469.578.750 C16.320.700.705 C17.800.621.430.530.550.625
|
| Concept/Terms |
Peutz-Jeghers Syndrome- Peutz-Jeghers Syndrome
- Peutz Jeghers Syndrome
- Syndrome, Peutz-Jeghers
- Polyposis, Hamartomatous Intestinal
- Hamartomatous Intestinal Polyposes
- Hamartomatous Intestinal Polyposis
- Intestinal Polyposes, Hamartomatous
- Intestinal Polyposis, Hamartomatous
- Polyposes, Hamartomatous Intestinal
- Peutz-Jegher's Syndrome
- Peutz Jegher's Syndrome
- Peutz-Jegher Syndrome
- Syndrome, Peutz-Jegher's
- Peutz-Jeghers Polyposis
- Peutz Jeghers Polyposis
- Polyposis, Peutz-Jeghers
- Periorificial Lentiginosis Syndrome
- Periorificial Lentiginosis Syndromes
- Syndrome, Periorificial Lentiginosis
- Syndromes, Periorificial Lentiginosis
- Lentiginosis, Perioral
- Lentiginoses, Perioral
- Perioral Lentiginoses
- Perioral Lentiginosis
- Polyps-and-Spots Syndrome
- Polyps and Spots Syndrome
- Polyps-and-Spots Syndromes
- Syndrome, Polyps-and-Spots
- Syndromes, Polyps-and-Spots
|
Below are MeSH descriptors whose meaning is more general than "Peutz-Jeghers Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Peutz-Jeghers Syndrome".
This graph shows the total number of publications written about "Peutz-Jeghers Syndrome" by people in this website by year, and whether "Peutz-Jeghers Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2000 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 2 | 0 | 2 |
| 2004 | 1 | 0 | 1 |
| 2005 | 1 | 1 | 2 |
| 2006 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2013 | 2 | 1 | 3 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Peutz-Jeghers Syndrome" by people in Profiles.
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Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group. Clin Cancer Res. 2024 Oct 15; 30(20):4566-4571.
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Hereditary ovarian tumour syndromes: current update on genetics and imaging. Clin Radiol. 2021 Apr; 76(4):313.e15-313.e26.
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Pancreatic Cancer Early Detection and Interception in an Atypical Case of Peutz-Jeghers Syndrome. Pancreas. 2019 04; 48(4):e29-e30.
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Pancreatic cancer screening in high-risk individuals with germline genetic mutations. Gastrointest Endosc. 2018 Jun; 87(6):1443-1450.
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Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood. Clin Cancer Res. 2017 07 01; 23(13):e107-e114.
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Endoscopic Submucosal Dissection of a Large Hamartoma in a Young Child. J Pediatr Gastroenterol Nutr. 2016 Jan; 62(1):e5-7.
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Findings from the Peutz-Jeghers syndrome registry of uruguay. PLoS One. 2013; 8(11):e79639.
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Risk factors for surgery in pediatric intussusception in the era of pneumatic reduction. J Pediatr Surg. 2013 May; 48(5):1032-6.
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Unusually early presentation of small-bowel adenocarcinoma in a patient with Peutz-Jeghers syndrome. J Pediatr Hematol Oncol. 2013 May; 35(4):323-8.
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Endocrine tumors associated with neurofibromatosis type 1, Peutz-Jeghers syndrome and other familial neoplasia syndromes. Front Horm Res. 2013; 41:166-81.