Peutz-Jeghers syndrome natural history, complications, and prognosis: Difference between revisions

Jump to navigation Jump to search
No edit summary
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{Peutz-Jeghers syndrome}}
{{Peutz-Jeghers syndrome}}
{{CMG}} {{AE}} {{MJK}}
{{CMG}} {{AE}} {{HQ}}


==Overview==
==Overview==
If left untreated, patients with Peutz-Jeghers syndrome may progress to develop [[rectal bleeding]], [[anemia]], [[intussusception]], [[bowel obstruction]], and [[abdominal pain]]. Common complications of Peutz-Jeghers syndrome include [[colon cancer]] and [[cachexia]].<ref>Zbuk KM, Eng C. Hamartomatous polyposis syndromes. Nat Clin Pract Gastroenterol Hepatol. 2007 Sep. 4(9):492-502.</ref>
If left untreated, patients with Peutz-Jeghers syndrome may progress to develop [[rectal bleeding]], [[anemia]], [[intussusception]], [[bowel obstruction]], and [[abdominal pain]]. Common complications of Peutz-Jeghers syndrome include [[colon cancer]] and [[cachexia]].
Prognosis is generally good with treatment.
Prognosis is generally good with treatment.


Line 11: Line 11:


==Complications==
==Complications==
Complications that can develop as a result of Peutz-Jeghers syndrome are:<ref>Complications of Peutz-Jeghers syndrome. Dr Amir Rezaee and Dr Alexandra Stanislavsky et al. Radiopaedia.org 2015. http://radiopaedia.org/articles/peutz-jeghers-syndrome-2</ref>
Complications that can develop as a result of Peutz-Jeghers syndrome are:<ref>Complications of Peutz-Jeghers syndrome. Dr Amir Rezaee and Dr Alexandra Stanislavsky et al. Radiopaedia.org 2015. http://radiopaedia.org/articles/peutz-jeghers-syndrome-2</ref><ref>Zbuk KM, Eng C. Hamartomatous polyposis syndromes. Nat Clin Pract Gastroenterol Hepatol. 2007 Sep. 4(9):492-502.</ref>
*[[Colon cancer]]
*[[Colon cancer]]
*[[Cachexia]]
*[[Cachexia]]

Revision as of 22:23, 15 December 2017

Peutz-Jeghers syndrome Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Peutz-Jeghers syndrome from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural history, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Chest X Ray

CT

MRI

Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Peutz-Jeghers syndrome natural history, complications, and prognosis On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Peutz-Jeghers syndrome natural history, complications, and prognosis

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Peutz-Jeghers syndrome natural history, complications, and prognosis

CDC on Peutz-Jeghers syndrome natural history, complications, and prognosis

Peutz-Jeghers syndrome natural history, complications, and prognosis in the news

Blogs on Peutz-Jeghers syndrome natural history, complications, and prognosis

Directions to Hospitals Treating Peutz-Jeghers syndrome

Risk calculators and risk factors for Peutz-Jeghers syndrome natural history, complications, and prognosis

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

Overview

If left untreated, patients with Peutz-Jeghers syndrome may progress to develop rectal bleeding, anemia, intussusception, bowel obstruction, and abdominal pain. Common complications of Peutz-Jeghers syndrome include colon cancer and cachexia. Prognosis is generally good with treatment.

Natural History

If left untreated, patients with Peutz-Jeghers syndrome may progress to develop rectal bleeding, anemia, intussusception, bowel obstruction, and abdominal pain.

Complications

Complications that can develop as a result of Peutz-Jeghers syndrome are:[1][2]

Prognosis

Prognosis is generally good with treatment. Almost half of Peutz-Jeghers patients die from cancer between age 50-60, and the cumulative risk of developing a form of cancer associated with Peutz-Jeghers syndrome between ages 15-64 is 93%.[4]

References

  1. Complications of Peutz-Jeghers syndrome. Dr Amir Rezaee and Dr Alexandra Stanislavsky et al. Radiopaedia.org 2015. http://radiopaedia.org/articles/peutz-jeghers-syndrome-2
  2. Zbuk KM, Eng C. Hamartomatous polyposis syndromes. Nat Clin Pract Gastroenterol Hepatol. 2007 Sep. 4(9):492-502.
  3. Butt N, Salih M, Khan MR, Ahmed R, Haider Z, Shah SH (2012). "An incidentally discovered asymptomatic para-aortic paraganglioma with Peutz-Jeghers syndrome". Saudi J Gastroenterol. 18 (6): 388–91. doi:10.4103/1319-3767.103432. PMC 3530995. PMID 23150026.
  4. Spigelman AD, Murday V, Phillips RK (1989). "Cancer and the Peutz-Jeghers syndrome". Gut. 30 (11): 1588–90. PMC 1434341. PMID 2599445.

Template:Digestive system neoplasia


Template:WH Template:WS