Cargando…

Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report

Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant condition characterized by hamartomatous polyps, primarily in the gastrointestinal tract and mucocutaneous pigmented macules. PJS patients are at an increased lifetime risk of malignancies and complications, such as gastrointestinal bleeding...

Descripción completa

Detalles Bibliográficos
Autores principales: Shakil, Sidra, Aldaher, Zackery, DiValentin, Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339141/
https://www.ncbi.nlm.nih.gov/pubmed/35919209
http://dx.doi.org/10.7759/cureus.26481
_version_ 1784760128415727616
author Shakil, Sidra
Aldaher, Zackery
DiValentin, Louis
author_facet Shakil, Sidra
Aldaher, Zackery
DiValentin, Louis
author_sort Shakil, Sidra
collection PubMed
description Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant condition characterized by hamartomatous polyps, primarily in the gastrointestinal tract and mucocutaneous pigmented macules. PJS patients are at an increased lifetime risk of malignancies and complications, such as gastrointestinal bleeding from polyposis. Routine screening is critical in patients diagnosed with PJS in order to avoid complications. We report a case of a 30-year-old female with PJS who had no family history presenting acutely due to gastrointestinal bleeding and poor surveillance of her condition.
format Online
Article
Text
id pubmed-9339141
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Cureus
record_format MEDLINE/PubMed
spelling pubmed-93391412022-08-01 Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report Shakil, Sidra Aldaher, Zackery DiValentin, Louis Cureus Internal Medicine Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant condition characterized by hamartomatous polyps, primarily in the gastrointestinal tract and mucocutaneous pigmented macules. PJS patients are at an increased lifetime risk of malignancies and complications, such as gastrointestinal bleeding from polyposis. Routine screening is critical in patients diagnosed with PJS in order to avoid complications. We report a case of a 30-year-old female with PJS who had no family history presenting acutely due to gastrointestinal bleeding and poor surveillance of her condition. Cureus 2022-07-01 /pmc/articles/PMC9339141/ /pubmed/35919209 http://dx.doi.org/10.7759/cureus.26481 Text en Copyright © 2022, Shakil et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Shakil, Sidra
Aldaher, Zackery
DiValentin, Louis
Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report
title Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report
title_full Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report
title_fullStr Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report
title_full_unstemmed Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report
title_short Peutz-Jeghers Syndrome Presenting With Anemia: A Case Report
title_sort peutz-jeghers syndrome presenting with anemia: a case report
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9339141/
https://www.ncbi.nlm.nih.gov/pubmed/35919209
http://dx.doi.org/10.7759/cureus.26481
work_keys_str_mv AT shakilsidra peutzjegherssyndromepresentingwithanemiaacasereport
AT aldaherzackery peutzjegherssyndromepresentingwithanemiaacasereport
AT divalentinlouis peutzjegherssyndromepresentingwithanemiaacasereport