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Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature
BACKGROUND: Pilonidal sinus is commonly seen at the sacrococcygeal region and few other sites, usually located at the midline, at areas where hairs collect or near protuberances or some adjacent rubbing surfaces. Its presence elsewhere is uncommon. We share an interesting case of a recurrent dischar...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874666/ https://www.ncbi.nlm.nih.gov/pubmed/33563340 http://dx.doi.org/10.1186/s13256-020-02561-z |
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author | Adhikari, B. N. Khatiwada, S. Bhattarai, A. |
author_facet | Adhikari, B. N. Khatiwada, S. Bhattarai, A. |
author_sort | Adhikari, B. N. |
collection | PubMed |
description | BACKGROUND: Pilonidal sinus is commonly seen at the sacrococcygeal region and few other sites, usually located at the midline, at areas where hairs collect or near protuberances or some adjacent rubbing surfaces. Its presence elsewhere is uncommon. We share an interesting case of a recurrent discharging sinus from the cheek bulge of a male which turned out to be a pilonidal sinus containing tuft of hairs on exploration and wide excision. CASE PRESENTATION: A 37 years old hirsute male presents to us with a non-healing discharging sinus at the bulge of the cheek. Exploration after a course of antibiotics showed 2 subcutaneous cavities with tuft of hairs. The area was excised along with a margin, thorough irrigation and curettage was done and the wound was closed primarily; a Z-plasty was incorporated in the central part to break the resultant suture line. Histopathological examination was done to confirm the diagnosis and rule out an off-midline dermoid cyst or an underlying/coexisting malignancy. Post-operative course was uneventful. The patient has been recurrence free for 1.5 years and is satisfied with the nature of the scar. CONCLUSIONS: Pilonidal sinus of the cheek bulge is an extremely rare entity. Complete excision and clinical suspicion are important for cure of this nagging ailment, especially at unexpected areas. |
format | Online Article Text |
id | pubmed-7874666 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78746662021-02-11 Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature Adhikari, B. N. Khatiwada, S. Bhattarai, A. J Med Case Rep Case Report BACKGROUND: Pilonidal sinus is commonly seen at the sacrococcygeal region and few other sites, usually located at the midline, at areas where hairs collect or near protuberances or some adjacent rubbing surfaces. Its presence elsewhere is uncommon. We share an interesting case of a recurrent discharging sinus from the cheek bulge of a male which turned out to be a pilonidal sinus containing tuft of hairs on exploration and wide excision. CASE PRESENTATION: A 37 years old hirsute male presents to us with a non-healing discharging sinus at the bulge of the cheek. Exploration after a course of antibiotics showed 2 subcutaneous cavities with tuft of hairs. The area was excised along with a margin, thorough irrigation and curettage was done and the wound was closed primarily; a Z-plasty was incorporated in the central part to break the resultant suture line. Histopathological examination was done to confirm the diagnosis and rule out an off-midline dermoid cyst or an underlying/coexisting malignancy. Post-operative course was uneventful. The patient has been recurrence free for 1.5 years and is satisfied with the nature of the scar. CONCLUSIONS: Pilonidal sinus of the cheek bulge is an extremely rare entity. Complete excision and clinical suspicion are important for cure of this nagging ailment, especially at unexpected areas. BioMed Central 2021-02-10 /pmc/articles/PMC7874666/ /pubmed/33563340 http://dx.doi.org/10.1186/s13256-020-02561-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Adhikari, B. N. Khatiwada, S. Bhattarai, A. Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature |
title | Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature |
title_full | Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature |
title_fullStr | Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature |
title_full_unstemmed | Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature |
title_short | Pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature |
title_sort | pilonidal sinus of the cheek: an extremely rare clinical entity—case report and brief review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874666/ https://www.ncbi.nlm.nih.gov/pubmed/33563340 http://dx.doi.org/10.1186/s13256-020-02561-z |
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