Peutz-Jeghers syndrome: Quantitative study on enterochromaffin cells in hamartomatous intestine polyps

Peutz-Jeghers syndrome: Quantitative study on enterochromaffin cells in hamartomatous intestine polyps

Introduction. Peutz-Jeghers (PJ) syndrome is a rare familial disorder with the autosomal transmission characterized by multiple intestinal polyps, mucocutaneous pigmentation and increased incidence of various malignancies. Some clinical manifestations of PJ syndrome may be associated with the se...

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Bibliographic Details
Main Authors: Krstić Miljan, Katić Vuka, Stojnev Slavica, Mihailović Dragan, Mojsilović Marijola, Radovanović Zoran, Živković Vladimir
Format: Article
Language:English
Published: Serbian Medical Society 2013-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
Peutz-Jeghers syndrome
hamartomatous polyp
enterochromaffin cells
chromogranin A
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2013/0370-81791310602K.pdf

Internet

http://www.doiserbia.nb.rs/img/doi/0370-8179/2013/0370-81791310602K.pdf

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