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Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review

INTRODUCTION AND IMPORTANCE: Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue, also called MALT lymphoma, is one of the entities of marginal zone lymphomas. These lymphomas are originated from indolent B-cell lymphomas and involve many organs such as the gastrointestinal tract,...

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Autores principales: Pham, Minh Duc, Nguyen, Minh Thao, Pham, Ngoc Trinh Thi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606698/
https://www.ncbi.nlm.nih.gov/pubmed/34840740
http://dx.doi.org/10.1016/j.amsu.2021.102973
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author Pham, Minh Duc
Nguyen, Minh Thao
Pham, Ngoc Trinh Thi
author_facet Pham, Minh Duc
Nguyen, Minh Thao
Pham, Ngoc Trinh Thi
author_sort Pham, Minh Duc
collection PubMed
description INTRODUCTION AND IMPORTANCE: Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue, also called MALT lymphoma, is one of the entities of marginal zone lymphomas. These lymphomas are originated from indolent B-cell lymphomas and involve many organs such as the gastrointestinal tract, salivary gland, skin, lung, thyroid or breast. Ileal MALT lymphoma is relatively rare and clinical symptoms are usually atypical. CASE PRESENTATION: We report a case of a 99-year-old man who admitted to the emergency department with increasing and colicky periumbilical pain, vomiting and constipation. Non-contrast-enhanced computed tomography suggested small bowel obstruction due to phytobezoar. Intraoperatively, surgeon discovered the tumor at the site of phytobezoar. Histologically, there was a diffuse infiltration comprised of small to medium sized lymphocytes with monocytoid features. Immunohistochemical result confirmed CD20 positive B-lymphocytes and the Ki-67 proliferation index was 10%. Ileal mucosa-associated lymphoid tissue lymphoma was diagnosed based on histological findings and immunohistochemistry. DISCUSSION: MALToma of the gastrointestinal tract is related to chronic antigenic, inflammatory bowel disease and malabsorption syndromes. However, the etiology of ileal MALToma is unclear. Moreover, symptom of ileal MALToma is really not typical and overleaped in the context of small intestinal obstruction. It should be differentiated small intestinal MALToma from immunoproliferative small intestinal disease and an alpha heavy chain disease. CONCLUSION: Ileal MALT lymphoma remains little known in many previous studies. It is really difficult to preoperatively diagnose. The combination of clinical presentation, postoperative histology and immunohistochemistry contribute to diagnosis and carry out appropriate management.
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spelling pubmed-86066982021-11-26 Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review Pham, Minh Duc Nguyen, Minh Thao Pham, Ngoc Trinh Thi Ann Med Surg (Lond) Case Report INTRODUCTION AND IMPORTANCE: Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue, also called MALT lymphoma, is one of the entities of marginal zone lymphomas. These lymphomas are originated from indolent B-cell lymphomas and involve many organs such as the gastrointestinal tract, salivary gland, skin, lung, thyroid or breast. Ileal MALT lymphoma is relatively rare and clinical symptoms are usually atypical. CASE PRESENTATION: We report a case of a 99-year-old man who admitted to the emergency department with increasing and colicky periumbilical pain, vomiting and constipation. Non-contrast-enhanced computed tomography suggested small bowel obstruction due to phytobezoar. Intraoperatively, surgeon discovered the tumor at the site of phytobezoar. Histologically, there was a diffuse infiltration comprised of small to medium sized lymphocytes with monocytoid features. Immunohistochemical result confirmed CD20 positive B-lymphocytes and the Ki-67 proliferation index was 10%. Ileal mucosa-associated lymphoid tissue lymphoma was diagnosed based on histological findings and immunohistochemistry. DISCUSSION: MALToma of the gastrointestinal tract is related to chronic antigenic, inflammatory bowel disease and malabsorption syndromes. However, the etiology of ileal MALToma is unclear. Moreover, symptom of ileal MALToma is really not typical and overleaped in the context of small intestinal obstruction. It should be differentiated small intestinal MALToma from immunoproliferative small intestinal disease and an alpha heavy chain disease. CONCLUSION: Ileal MALT lymphoma remains little known in many previous studies. It is really difficult to preoperatively diagnose. The combination of clinical presentation, postoperative histology and immunohistochemistry contribute to diagnosis and carry out appropriate management. Elsevier 2021-10-30 /pmc/articles/PMC8606698/ /pubmed/34840740 http://dx.doi.org/10.1016/j.amsu.2021.102973 Text en © 2021 The Authors https://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
Pham, Minh Duc
Nguyen, Minh Thao
Pham, Ngoc Trinh Thi
Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review
title Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review
title_full Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review
title_fullStr Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review
title_full_unstemmed Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review
title_short Ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: A case report and literature review
title_sort ileal mucosa-associated lymphoid tissue lymphoma diagnosed after emergency surgery: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606698/
https://www.ncbi.nlm.nih.gov/pubmed/34840740
http://dx.doi.org/10.1016/j.amsu.2021.102973
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