Cargando…
A Rare Case of Duodenal Melanosis: Case Report
Pseudomelanosis (PM) is a rare condition of unknown etiology and pathogenesis, described as speckled black pigmentation of intestinal mucosa. It is usually discovered as an incidental finding during endoscopy. Although, etiology of PM is unclear, it has been associated with different medications and...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567319/ https://www.ncbi.nlm.nih.gov/pubmed/33083177 http://dx.doi.org/10.7759/cureus.10475 |
_version_ | 1783596303055323136 |
---|---|
author | Rana, Navpreet K Minhas, Umair Mahl, Thomas |
author_facet | Rana, Navpreet K Minhas, Umair Mahl, Thomas |
author_sort | Rana, Navpreet K |
collection | PubMed |
description | Pseudomelanosis (PM) is a rare condition of unknown etiology and pathogenesis, described as speckled black pigmentation of intestinal mucosa. It is usually discovered as an incidental finding during endoscopy. Although, etiology of PM is unclear, it has been associated with different medications and systemic diseases such as chronic renal disease and diabetes mellitus. In this report, we describe a case of a 72-year-old male with multiple co-morbidities who presented with epigastric pain, nausea and hematemesis. Subsequently, upper endoscopy performed revealed intestinal PM with no active bleeding. Although considered a benign condition, knowing the existence of PM is important to exclude other serious conditions with similar endoscopic findings. |
format | Online Article Text |
id | pubmed-7567319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-75673192020-10-19 A Rare Case of Duodenal Melanosis: Case Report Rana, Navpreet K Minhas, Umair Mahl, Thomas Cureus Endocrinology/Diabetes/Metabolism Pseudomelanosis (PM) is a rare condition of unknown etiology and pathogenesis, described as speckled black pigmentation of intestinal mucosa. It is usually discovered as an incidental finding during endoscopy. Although, etiology of PM is unclear, it has been associated with different medications and systemic diseases such as chronic renal disease and diabetes mellitus. In this report, we describe a case of a 72-year-old male with multiple co-morbidities who presented with epigastric pain, nausea and hematemesis. Subsequently, upper endoscopy performed revealed intestinal PM with no active bleeding. Although considered a benign condition, knowing the existence of PM is important to exclude other serious conditions with similar endoscopic findings. Cureus 2020-09-15 /pmc/articles/PMC7567319/ /pubmed/33083177 http://dx.doi.org/10.7759/cureus.10475 Text en Copyright © 2020, Rana et al. http://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 | Endocrinology/Diabetes/Metabolism Rana, Navpreet K Minhas, Umair Mahl, Thomas A Rare Case of Duodenal Melanosis: Case Report |
title | A Rare Case of Duodenal Melanosis: Case Report |
title_full | A Rare Case of Duodenal Melanosis: Case Report |
title_fullStr | A Rare Case of Duodenal Melanosis: Case Report |
title_full_unstemmed | A Rare Case of Duodenal Melanosis: Case Report |
title_short | A Rare Case of Duodenal Melanosis: Case Report |
title_sort | rare case of duodenal melanosis: case report |
topic | Endocrinology/Diabetes/Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567319/ https://www.ncbi.nlm.nih.gov/pubmed/33083177 http://dx.doi.org/10.7759/cureus.10475 |
work_keys_str_mv | AT rananavpreetk ararecaseofduodenalmelanosiscasereport AT minhasumair ararecaseofduodenalmelanosiscasereport AT mahlthomas ararecaseofduodenalmelanosiscasereport AT rananavpreetk rarecaseofduodenalmelanosiscasereport AT minhasumair rarecaseofduodenalmelanosiscasereport AT mahlthomas rarecaseofduodenalmelanosiscasereport |