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Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India
INTRODUCTION: Trichobezoars are concretions formed by accumulation of hair in stomach. Usually, trichobezoar is confined to the stomach, but rarely it may extend from the stomach to the small intestine and even colon. This is an unusual form called Rapunzel syndrome. Our experience with this rare en...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602516/ https://www.ncbi.nlm.nih.gov/pubmed/28918296 http://dx.doi.org/10.1016/j.ijscr.2017.08.060 |
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author | Kajal, Pradeep Bhutani, Namita Tyagi, Niharika Arya, Pratibha |
author_facet | Kajal, Pradeep Bhutani, Namita Tyagi, Niharika Arya, Pratibha |
author_sort | Kajal, Pradeep |
collection | PubMed |
description | INTRODUCTION: Trichobezoars are concretions formed by accumulation of hair in stomach. Usually, trichobezoar is confined to the stomach, but rarely it may extend from the stomach to the small intestine and even colon. This is an unusual form called Rapunzel syndrome. Our experience with this rare entity of Rapunzel syndrome and interesting entity of trichobezoar is being presented with review of literature. PRESENTATION OF CASES: We, at our institute, encountered four cases of trichobezoar in last five years, out of which two were found to be of Rapunzel syndrome. All of these cases were managed successfully by open surgical intervention in view of the very large size of the mass in all the cases. DISCUSSION: The clinical presentation is highly variable ranging from asymptomatic cases diagnosed incidently to serious gastrointestinal symptoms and complications. Cases of trichobezoar have been reported in literature very infrequently but Rapunzel syndrome is extremely rare and less than 50 cases have been reported in medical literature till date. CONCLUSION: Trichobezoar leading to Rapunzel syndrome is an extremely rare entity. The clinical presentation is usually vague and non-specific. Treatment is mainly surgical because of delayed presentation in majority of the cases. Psychiatric illness is the usual association. |
format | Online Article Text |
id | pubmed-5602516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56025162017-09-25 Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India Kajal, Pradeep Bhutani, Namita Tyagi, Niharika Arya, Pratibha Int J Surg Case Rep Case Series INTRODUCTION: Trichobezoars are concretions formed by accumulation of hair in stomach. Usually, trichobezoar is confined to the stomach, but rarely it may extend from the stomach to the small intestine and even colon. This is an unusual form called Rapunzel syndrome. Our experience with this rare entity of Rapunzel syndrome and interesting entity of trichobezoar is being presented with review of literature. PRESENTATION OF CASES: We, at our institute, encountered four cases of trichobezoar in last five years, out of which two were found to be of Rapunzel syndrome. All of these cases were managed successfully by open surgical intervention in view of the very large size of the mass in all the cases. DISCUSSION: The clinical presentation is highly variable ranging from asymptomatic cases diagnosed incidently to serious gastrointestinal symptoms and complications. Cases of trichobezoar have been reported in literature very infrequently but Rapunzel syndrome is extremely rare and less than 50 cases have been reported in medical literature till date. CONCLUSION: Trichobezoar leading to Rapunzel syndrome is an extremely rare entity. The clinical presentation is usually vague and non-specific. Treatment is mainly surgical because of delayed presentation in majority of the cases. Psychiatric illness is the usual association. Elsevier 2017-09-08 /pmc/articles/PMC5602516/ /pubmed/28918296 http://dx.doi.org/10.1016/j.ijscr.2017.08.060 Text en © 2017 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Series Kajal, Pradeep Bhutani, Namita Tyagi, Niharika Arya, Pratibha Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India |
title | Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India |
title_full | Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India |
title_fullStr | Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India |
title_full_unstemmed | Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India |
title_short | Trichobezoar with and without Rapunzel syndrome in paediatric population: A case series from a tertiary care centre of Northern India |
title_sort | trichobezoar with and without rapunzel syndrome in paediatric population: a case series from a tertiary care centre of northern india |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5602516/ https://www.ncbi.nlm.nih.gov/pubmed/28918296 http://dx.doi.org/10.1016/j.ijscr.2017.08.060 |
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