<abstract xmlns="http://www.w3.org/1999/xhtml">

<p>Burkitt lymphoma (BL) is a highly aggressive mature B-cell neoplasm with the highest incidence in a pediatric population. Three clinical subtypes of BL are known: sporadic, endemic, and immune deficiency associated. The most common site of involvement in the case of the sporadic form is an ileocecal region. We describe a rare case of sporadic BL in a 71-year-old male with a primary localisation in the rectum presenting with progressive bowel obstruction and rectal bleeding. The clinical evaluation involved colonoscopy, biopsy with a following morphological examination, computerised tomography of thorax, abdomen and pelvis, magnetic resonance imaging of pelvis, and laboratory analysis. Due to the unclear tumorous mass and progressive clinical symptoms, surgical treatment was applied – laparotomy, total mesorectal excision with the formation of permanent colostomy. Morphological examination of the specimen revealed a phenotype characteristic to BL. One month after the surgery, two single liver metastasis were detected. The patient received six courses of DA-EPOCH chemotherapy. Post-treatment radiological examinations revealed full clinical remission and disease-free survival for 68 months (5 years and 8 months).</p>
</abstract>

Burkitt lymphoma (BL) is a highly aggressive mature B-cell neoplasm with the highest incidence in a pediatric population. Three clinical subtypes of BL are known: sporadic, endemic, and immune deficiency associated. The most common site of involvement in the case of the sporadic form is an ileocecal region. We describe a rare case of sporadic BL in a 71-year-old male with a primary localisation in the rectum presenting with progressive bowel obstruction and rectal bleeding. The clinical evaluation involved colonoscopy, biopsy with a following morphological examination, computerised tomography of thorax, abdomen and pelvis, magnetic resonance imaging of pelvis, and laboratory analysis. Due to the unclear tumorous mass and progressive clinical symptoms, surgical treatment was applied – laparotomy, total mesorectal excision with the formation of permanent colostomy. Morphological examination of the specimen revealed a phenotype characteristic to BL. One month after the surgery, two single liver metastasis were detected. The patient received six courses of DA-EPOCH chemotherapy. Post-treatment radiological examinations revealed full clinical remission and disease-free survival for 68 months (5 years and 8 months).

Primary Burkitt Lymphoma of the Rectum

Pauls Stradiņš Clinical University Hospital

Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.

This work is licensed under the Creative Commons Attribution 4.0 International License.

{"article-title":"Primary Burkitt Lymphoma of the Rectum"}

Burkitt lymphoma (BL) is a highly aggressive mature B-cell neoplasm with the highest incidence in a pediatric population. Three clinical subtypes of BL are...

Primary Burkitt Lymphoma of the Rectum

Pubblicato online: 28 set 2023

Pagine: 211 - 216

Ricevuto: 21 nov 2021

Accettato: 21 apr 2023

DOI: https://doi.org/10.2478/prolas-2023-0029

Parole chiave
Burkitt lymphoma, sporadic, gastrointestinal, rectal neoplasm, bowel obstruction

© 2023 Linda Kokaine et al., published by Sciendo

This work is licensed under the Creative Commons Attribution 4.0 International License.

Primary Burkitt Lymphoma of the Rectum

Pubblicato online: 28 set 2023

Pagine: 211 - 216

Ricevuto: 21 nov 2021

Accettato: 21 apr 2023

DOI: https://doi.org/10.2478/prolas-2023-0029

Parole chiaveBurkitt lymphoma, sporadic, gastrointestinal, rectal neoplasm, bowel obstruction

© 2023 Linda Kokaine et al., published by Sciendo

This work is licensed under the Creative Commons Attribution 4.0 International License.

Parole chiave
Burkitt lymphoma, sporadic, gastrointestinal, rectal neoplasm, bowel obstruction