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Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity
INTRODUCTION: Inflammatory myo-fibroblastic tumor of appendix is one of the rarest clinical findings and less has been described in the literatures. So, we aimed to present the clinical case that we encountered at our institute. PRESENTATION OF A CASE: A 29-year-old lady presented with history of pa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627983/ https://www.ncbi.nlm.nih.gov/pubmed/34823164 http://dx.doi.org/10.1016/j.ijscr.2021.106607 |
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author | Baral, Suman Karki, Om Bahadur Poudel, Suman Bhattarai, Subash Poudel, Puskar |
author_facet | Baral, Suman Karki, Om Bahadur Poudel, Suman Bhattarai, Subash Poudel, Puskar |
author_sort | Baral, Suman |
collection | PubMed |
description | INTRODUCTION: Inflammatory myo-fibroblastic tumor of appendix is one of the rarest clinical findings and less has been described in the literatures. So, we aimed to present the clinical case that we encountered at our institute. PRESENTATION OF A CASE: A 29-year-old lady presented with history of pain at the periumbilical area for one day which shifted to right iliac fossa. Clinical examination revealed tenderness and rebound at right iliac fossa with increased total leucocyte count and ultrasonography abdomen showed swollen appendix. Intraoperatively, a lump around 4 × 3 cm was evident at the tip of appendix with cut section revealing pus along with fecalith. Appendectomy was done with no spillage of the content within the peritoneal cavity. Histopathology revealed inflammatory myo-fibroblastic tumor of appendix. Patient is on regular follow up. DISCUSSION: Inflammatory myo-fibroblastic tumor of appendix is one of the rarest clinical findings that mimics malignancy. Presentation could be that of acute appendicitis and in most instances, diagnosis is made intraoperatively. Surgical removal is the mainstay of treatment with regular follow up of the patient for chances of recurrences. Histologically, edematous stroma consisting of inflammatory infiltrates composed of lymphocytes, plasma cells, eosinophils and focal formation of lymphoid follicles along with the proliferation of scattered spindle to ovoid cells with proliferating blood vessels with unremarkable over lying epithelium is evident. Myo-fibroblastic origin can be confirmed by immunostaining with smooth muscle specific vimentin and actin. CONCLUSION: Inflammatory myo-fibroblastic tumor of appendix can present with features of acute appendicitis and may mimic malignancy. Appendectomy with regular follow up is mandated if such clinical cases are encountered. |
format | Online Article Text |
id | pubmed-8627983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-86279832021-12-06 Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity Baral, Suman Karki, Om Bahadur Poudel, Suman Bhattarai, Subash Poudel, Puskar Int J Surg Case Rep Case Report INTRODUCTION: Inflammatory myo-fibroblastic tumor of appendix is one of the rarest clinical findings and less has been described in the literatures. So, we aimed to present the clinical case that we encountered at our institute. PRESENTATION OF A CASE: A 29-year-old lady presented with history of pain at the periumbilical area for one day which shifted to right iliac fossa. Clinical examination revealed tenderness and rebound at right iliac fossa with increased total leucocyte count and ultrasonography abdomen showed swollen appendix. Intraoperatively, a lump around 4 × 3 cm was evident at the tip of appendix with cut section revealing pus along with fecalith. Appendectomy was done with no spillage of the content within the peritoneal cavity. Histopathology revealed inflammatory myo-fibroblastic tumor of appendix. Patient is on regular follow up. DISCUSSION: Inflammatory myo-fibroblastic tumor of appendix is one of the rarest clinical findings that mimics malignancy. Presentation could be that of acute appendicitis and in most instances, diagnosis is made intraoperatively. Surgical removal is the mainstay of treatment with regular follow up of the patient for chances of recurrences. Histologically, edematous stroma consisting of inflammatory infiltrates composed of lymphocytes, plasma cells, eosinophils and focal formation of lymphoid follicles along with the proliferation of scattered spindle to ovoid cells with proliferating blood vessels with unremarkable over lying epithelium is evident. Myo-fibroblastic origin can be confirmed by immunostaining with smooth muscle specific vimentin and actin. CONCLUSION: Inflammatory myo-fibroblastic tumor of appendix can present with features of acute appendicitis and may mimic malignancy. Appendectomy with regular follow up is mandated if such clinical cases are encountered. Elsevier 2021-11-22 /pmc/articles/PMC8627983/ /pubmed/34823164 http://dx.doi.org/10.1016/j.ijscr.2021.106607 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Baral, Suman Karki, Om Bahadur Poudel, Suman Bhattarai, Subash Poudel, Puskar Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity |
title | Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity |
title_full | Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity |
title_fullStr | Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity |
title_full_unstemmed | Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity |
title_short | Inflammatory myo-fibroblastic tumor of appendix: A rare clinical entity |
title_sort | inflammatory myo-fibroblastic tumor of appendix: a rare clinical entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627983/ https://www.ncbi.nlm.nih.gov/pubmed/34823164 http://dx.doi.org/10.1016/j.ijscr.2021.106607 |
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