Peutz-Jeghers syndrome screening: Difference between revisions

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{{Peutz-Jeghers syndrome}}
{{Peutz-Jeghers syndrome}}


{{CMG}} {{AE}} {{HQ}}
{{CMG}}; {{AE}} {{HQ}}


==Overview==
==Overview==
Screening for cancerous lesions by small intestine radiography, [[esophagogastroduodenoscopy]] (EGD), [[colonoscopy]], [[pancreatic]] [[ultrasound]], [[pelvic ultrasound]], [[mammography]], and [[Pap test|Papanicolaou test]] ([[Pap test]]) is recommended among patients with Peutz-Jeghers syndrome.
Screening for [[cancerous]] lesions by [[small intestine]] [[radiography]], [[esophagogastroduodenoscopy]] ([[EGD]]), [[colonoscopy]], [[pancreatic]] [[ultrasound]], [[pelvic ultrasound]], [[mammography]], and [[Pap test|Papanicolaou test]] ([[Pap test]]) is recommended among patients with Peutz-Jeghers syndrome.


==Screening==
==Screening==
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*[[Enteroclysis]]
*[[Enteroclysis]]
*[[Colonoscopy]]
*[[Colonoscopy]]
At time of diagnosis, screening for cancerous lesions among patients with Peutz-Jeghers syndrome include the following:<ref name="SyngalBrand2015">{{cite journal|last1=Syngal|first1=Sapna|last2=Brand|first2=Randall E|last3=Church|first3=James M|last4=Giardiello|first4=Francis M|last5=Hampel|first5=Heather L|last6=Burt|first6=Randall W|title=ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes|journal=The American Journal of Gastroenterology|volume=110|issue=2|year=2015|pages=223–262|issn=0002-9270|doi=10.1038/ajg.2014.435}}</ref>
*Small bowel video capsule endoscopy (every 3 years)
*Stomach [[Esophagogastroduodenoscopy]] (every 3 years)
*[[Colonoscopy]] (every 3 years)
*Pancreas (every 1-2 years)
**[[Endoscopic ultrasound]] OR
**[[Magnetic resonance cholangiopancreatography]] (MRCP)
*Abdominal [[CT]]
*[[Pelvic ultrasound]] (annually)
*Testicular exam (annually)
**If abnormalities palpable perform an ultrasound
*[[Mammography]] starting at age 25 (annually)
*Endometrial pelvic exam and ultrasound (annually)
*Cervical Papanicolaou test ([[Pap test]]) (annually).
*Physical examination that includes evaluation of the [[breasts]], [[abdomen]], [[pelvis]], and [[testes]] should be performed by a physician (annually)
*Complete blood count ([[CBC]]) to check for anemia should be done (annually)


== References ==
== References ==
{{reflist|2}}
{{reflist|2}}
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[[Category:Gastroenterology]]
[[Category:Surgery]]
[[Category:Oncology]]
[[Category:Disease]]
[[Category:Pediatrics]]
[[Category:Up-To-Date]]

Latest revision as of 16:43, 21 December 2017

Peutz-Jeghers syndrome Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]

Overview

Screening for cancerous lesions by small intestine radiography, esophagogastroduodenoscopy (EGD), colonoscopy, pancreatic ultrasound, pelvic ultrasound, mammography, and Papanicolaou test (Pap test) is recommended among patients with Peutz-Jeghers syndrome.

Screening

Patients who are at risk of developing Peutz-Jeghers syndrome are screened for the locations of the hamartomas by:[1]

References

  1. Syngal, Sapna; Brand, Randall E; Church, James M; Giardiello, Francis M; Hampel, Heather L; Burt, Randall W (2015). "ACG Clinical Guideline: Genetic Testing and Management of Hereditary Gastrointestinal Cancer Syndromes". The American Journal of Gastroenterology. 110 (2): 223–262. doi:10.1038/ajg.2014.435. ISSN 0002-9270.

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