Peutz-Jeghers syndrome pathophysiology: Difference between revisions

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===Gross Pathology===
===Gross Pathology===
Peutz-Jeghers [[polyps]] are non neoplastic [[hamartomas]] due to proliferation of all three layers of the [[mucosa]], which have a characteristic feature of a [[smooth muscle]] core continuous with [[muscularis mucosa]] in a tree-like branching pattern.
Peutz-Jeghers [[polyps]] are non neoplastic [[hamartomas]] due to proliferation of all three layers of the [[mucosa]], which have a characteristic feature of a [[smooth muscle]] core continuous with [[muscularis mucosa]] in a tree-like branching pattern.
===Microscopic Pathology===
On microscopic histopathological analysis, polyps have the following characteristic findings:
*Frond-like polyp with all three components of mucosa:
:*Muscosal epithelium (melanotic mucosa, goblet cells)
:*Lamina propria
:*Muscularis mucosae


== References ==
== References ==

Revision as of 14:00, 14 September 2015

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Peutz-Jeghers syndrome is transmitted in autosomal dominant pattern.

Pathophysiology

Genetics

Peutz-Jeghers syndrome is caused by a mutation in STK11 (LKB1) tumor suppressor gene on chromosome 19.[1] It is inherited in an autosomal dominant pattern, which means that anyone who has Peutz-Jeghers syndrome (PJS) has a 50% chance of passing it onto his/her offspring.

Gross Pathology

Peutz-Jeghers polyps are non neoplastic hamartomas due to proliferation of all three layers of the mucosa, which have a characteristic feature of a smooth muscle core continuous with muscularis mucosa in a tree-like branching pattern.

Microscopic Pathology

On microscopic histopathological analysis, polyps have the following characteristic findings:

  • Frond-like polyp with all three components of mucosa:
  • Muscosal epithelium (melanotic mucosa, goblet cells)
  • Lamina propria
  • Muscularis mucosae

References

  1. JBouquot, Jerry E.; Neville, Brad W.; Damm, Douglas D.; Allen, Carl P. (2008).Oral and Maxillofacial Pathology. Philadelphia: Saunders. p.16.11.ISBN1-4160-3435-8.

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