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Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination

INTRODUCTION: Primary NHL (non-Hodgkin lymphoma) of the colon represents only 0.2% to 1.2% of all colonic malignancies. Burkitt's lymphoma (BL) is usually a disease reported in children and young people, most of them associated with EBV or HIV infection. We describe a rare case of intestinal ob...

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Autores principales: Panaccio, Paolo, Fiordaliso, Michele, Testa, Domenica, Mazzola, Lorenzo, Battilana, Mariangela, Cotellese, Roberto, Selvaggi, Federico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952441/
https://www.ncbi.nlm.nih.gov/pubmed/29854542
http://dx.doi.org/10.1155/2018/6265182
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author Panaccio, Paolo
Fiordaliso, Michele
Testa, Domenica
Mazzola, Lorenzo
Battilana, Mariangela
Cotellese, Roberto
Selvaggi, Federico
author_facet Panaccio, Paolo
Fiordaliso, Michele
Testa, Domenica
Mazzola, Lorenzo
Battilana, Mariangela
Cotellese, Roberto
Selvaggi, Federico
author_sort Panaccio, Paolo
collection PubMed
description INTRODUCTION: Primary NHL (non-Hodgkin lymphoma) of the colon represents only 0.2% to 1.2% of all colonic malignancies. Burkitt's lymphoma (BL) is usually a disease reported in children and young people, most of them associated with EBV or HIV infection. We describe a rare case of intestinal obstruction due to sporadic Burkitt's lymphoma causing ileocaecal invagination explaining our experience Methods. A 31-year-old man presented with diffuse colic pain and weight loss. Clinical examination revealed an abdominal distension with pain in the right iliac fossa. Colonoscopy documented a caecal large lesion with ulcerated mucosa. Computed tomography (CT) have shown a 60 × 50 mm right colic parietal lesion with signs of ileocolic intussusception. RESULTS: Laparoscopic right hemicolectomy was performed. Postoperative period was uneventful. CD20+ high-grade B-cell Burkitt's lymphoma was confirmed by immunohistochemistry (CD20+, CD79+, and CD10+) and FISH test (t (8;14) (q24; q32). The patient was subsequently treated with adjuvant combination chemotherapy (Hyper-CVAD) and is alive and disease-free at 8 months follow-up. DISCUSSION: Adult sporadic Burkitt's lymphoma (BL) causing intestinal obstruction due to ileocaecal intussusception is an extremely rare occurrence and a diagnostic dilemma. Despite the surgical approach is selected based on patient's conditions and surgeon's expertise, minimally invasive method could be preferred.
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spelling pubmed-59524412018-05-31 Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination Panaccio, Paolo Fiordaliso, Michele Testa, Domenica Mazzola, Lorenzo Battilana, Mariangela Cotellese, Roberto Selvaggi, Federico Case Rep Surg Case Report INTRODUCTION: Primary NHL (non-Hodgkin lymphoma) of the colon represents only 0.2% to 1.2% of all colonic malignancies. Burkitt's lymphoma (BL) is usually a disease reported in children and young people, most of them associated with EBV or HIV infection. We describe a rare case of intestinal obstruction due to sporadic Burkitt's lymphoma causing ileocaecal invagination explaining our experience Methods. A 31-year-old man presented with diffuse colic pain and weight loss. Clinical examination revealed an abdominal distension with pain in the right iliac fossa. Colonoscopy documented a caecal large lesion with ulcerated mucosa. Computed tomography (CT) have shown a 60 × 50 mm right colic parietal lesion with signs of ileocolic intussusception. RESULTS: Laparoscopic right hemicolectomy was performed. Postoperative period was uneventful. CD20+ high-grade B-cell Burkitt's lymphoma was confirmed by immunohistochemistry (CD20+, CD79+, and CD10+) and FISH test (t (8;14) (q24; q32). The patient was subsequently treated with adjuvant combination chemotherapy (Hyper-CVAD) and is alive and disease-free at 8 months follow-up. DISCUSSION: Adult sporadic Burkitt's lymphoma (BL) causing intestinal obstruction due to ileocaecal intussusception is an extremely rare occurrence and a diagnostic dilemma. Despite the surgical approach is selected based on patient's conditions and surgeon's expertise, minimally invasive method could be preferred. Hindawi 2018-04-30 /pmc/articles/PMC5952441/ /pubmed/29854542 http://dx.doi.org/10.1155/2018/6265182 Text en Copyright © 2018 Paolo Panaccio et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Panaccio, Paolo
Fiordaliso, Michele
Testa, Domenica
Mazzola, Lorenzo
Battilana, Mariangela
Cotellese, Roberto
Selvaggi, Federico
Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination
title Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination
title_full Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination
title_fullStr Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination
title_full_unstemmed Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination
title_short Minimally Invasive Treatment of Sporadic Burkitt's Lymphoma Causing Ileocaecal Invagination
title_sort minimally invasive treatment of sporadic burkitt's lymphoma causing ileocaecal invagination
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952441/
https://www.ncbi.nlm.nih.gov/pubmed/29854542
http://dx.doi.org/10.1155/2018/6265182
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