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Perianal pseudolymphoma: A case report and review of the literature

INTRODUCTION: Perianal pseudolymphoma is a rare lymphoproliferative disorder that can mimic cutaneous lymphoma. The condition can present acutely with concerns of perianal sepsis. The purpose of this case review is to review the current literature on perianal pseudolymphoma and emphasise to the surg...

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Autores principales: Cuda, Tahleesa, Prinsloo, Pieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587893/
https://www.ncbi.nlm.nih.gov/pubmed/28881336
http://dx.doi.org/10.1016/j.ijscr.2017.08.014
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author Cuda, Tahleesa
Prinsloo, Pieter
author_facet Cuda, Tahleesa
Prinsloo, Pieter
author_sort Cuda, Tahleesa
collection PubMed
description INTRODUCTION: Perianal pseudolymphoma is a rare lymphoproliferative disorder that can mimic cutaneous lymphoma. The condition can present acutely with concerns of perianal sepsis. The purpose of this case review is to review the current literature on perianal pseudolymphoma and emphasise to the surgical community its presentation, suggested aetiology and management. CASE PRESENTATION: In this case report, we detail the case of a 28-year-old female who presented with perianal pseudolymphoma. Malignant lymphoproliferative diseases required exclusion. Conservative management of this rare condition was successful. DISCUSSION: We highlight the differential diagnoses, investigations and treatment options for a rare condition. A review of the literature on the limited published data on perianal pseudolymphoma is briefly discussed. CONCLUSION: The aim of this case report is to highlight the existence of such a rare condition that can imitate an acute surgical presentation and its successful conservative management.
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spelling pubmed-55878932017-09-14 Perianal pseudolymphoma: A case report and review of the literature Cuda, Tahleesa Prinsloo, Pieter Int J Surg Case Rep Case Report INTRODUCTION: Perianal pseudolymphoma is a rare lymphoproliferative disorder that can mimic cutaneous lymphoma. The condition can present acutely with concerns of perianal sepsis. The purpose of this case review is to review the current literature on perianal pseudolymphoma and emphasise to the surgical community its presentation, suggested aetiology and management. CASE PRESENTATION: In this case report, we detail the case of a 28-year-old female who presented with perianal pseudolymphoma. Malignant lymphoproliferative diseases required exclusion. Conservative management of this rare condition was successful. DISCUSSION: We highlight the differential diagnoses, investigations and treatment options for a rare condition. A review of the literature on the limited published data on perianal pseudolymphoma is briefly discussed. CONCLUSION: The aim of this case report is to highlight the existence of such a rare condition that can imitate an acute surgical presentation and its successful conservative management. Elsevier 2017-08-17 /pmc/articles/PMC5587893/ /pubmed/28881336 http://dx.doi.org/10.1016/j.ijscr.2017.08.014 Text en © 2017 The Author(s) 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 Report
Cuda, Tahleesa
Prinsloo, Pieter
Perianal pseudolymphoma: A case report and review of the literature
title Perianal pseudolymphoma: A case report and review of the literature
title_full Perianal pseudolymphoma: A case report and review of the literature
title_fullStr Perianal pseudolymphoma: A case report and review of the literature
title_full_unstemmed Perianal pseudolymphoma: A case report and review of the literature
title_short Perianal pseudolymphoma: A case report and review of the literature
title_sort perianal pseudolymphoma: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587893/
https://www.ncbi.nlm.nih.gov/pubmed/28881336
http://dx.doi.org/10.1016/j.ijscr.2017.08.014
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