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Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports
BACKGROUND: Pediatric-type follicular lymphoma (PTFL) is a unique pathological type in the 4(th) edition of hematopoiesis and lymphoid tissue tumor classification revised by World Health Organization. It is unique in clinical practice and seldom seen in adult. PTFL mainly occurs in the head and neck...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610869/ https://www.ncbi.nlm.nih.gov/pubmed/34877288 http://dx.doi.org/10.12998/wjcc.v9.i31.9542 |
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author | Liu, Yao Xing, Hui Liu, Yue-Ping |
author_facet | Liu, Yao Xing, Hui Liu, Yue-Ping |
author_sort | Liu, Yao |
collection | PubMed |
description | BACKGROUND: Pediatric-type follicular lymphoma (PTFL) is a unique pathological type in the 4(th) edition of hematopoiesis and lymphoid tissue tumor classification revised by World Health Organization. It is unique in clinical practice and seldom seen in adult. PTFL mainly occurs in the head and neck lymph nodes. Most of the cases are short of fever, night sweat, weight loss, and other B symptoms which substitute for lymphadenopathy as the main symptom. PTFL can be disposed of surgical resection and it can achieve long-term tumor-free survival, and it has an excellent outcome. CASE SUMMARY: Two cases of PTFL were reported and their clinicopathological features, differential diagnosis, therapy and prognosis were discussed. PTFL showed gray-brown tough texture in general performance. The histological manifestations of PTFL were similar to that of adult-follicular lymphoma (FL). Under low power microscope, the structure of lymph nodes was destroyed in different degree, the follicles were closely arranged, expanded and irregular, and the mantle zone became thin or disappeared. In addition, the “starry sky phenomenon” could be seen. At high magnification, the follicles were mainly composed of single medium-sized central cells, and some of them mainly consisted of centroblastic cells to characterize scattered chromatin and inconspicuous nucleoli. Immunohistochemical showed the tumor cells expressed CD20, PAX5, CD79a and CD10, BCL6, FOXP-1, which were limited in germinal center; Ki-67 was highly expressed in germinal center. CD21 and CD23 showed nodular and expanded follicular dendritic cells. Immunoglobulin gene rearrangement was positive for IGH and IGK. The two patients underwent surgical resection with no complications. After discharge, the two patients with a close review for 18 mo and 5 mo respectively and showed no evidence of recurrence. CONCLUSION: PTFL in adult is generally supposed to be extremely rare. PTFL displayed characteristic morphological, immunophenotypic, and molecular biological changes which are a kind of neoplasm with satisfactory prognosis after surgical excision. |
format | Online Article Text |
id | pubmed-8610869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-86108692021-12-06 Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports Liu, Yao Xing, Hui Liu, Yue-Ping World J Clin Cases Case Report BACKGROUND: Pediatric-type follicular lymphoma (PTFL) is a unique pathological type in the 4(th) edition of hematopoiesis and lymphoid tissue tumor classification revised by World Health Organization. It is unique in clinical practice and seldom seen in adult. PTFL mainly occurs in the head and neck lymph nodes. Most of the cases are short of fever, night sweat, weight loss, and other B symptoms which substitute for lymphadenopathy as the main symptom. PTFL can be disposed of surgical resection and it can achieve long-term tumor-free survival, and it has an excellent outcome. CASE SUMMARY: Two cases of PTFL were reported and their clinicopathological features, differential diagnosis, therapy and prognosis were discussed. PTFL showed gray-brown tough texture in general performance. The histological manifestations of PTFL were similar to that of adult-follicular lymphoma (FL). Under low power microscope, the structure of lymph nodes was destroyed in different degree, the follicles were closely arranged, expanded and irregular, and the mantle zone became thin or disappeared. In addition, the “starry sky phenomenon” could be seen. At high magnification, the follicles were mainly composed of single medium-sized central cells, and some of them mainly consisted of centroblastic cells to characterize scattered chromatin and inconspicuous nucleoli. Immunohistochemical showed the tumor cells expressed CD20, PAX5, CD79a and CD10, BCL6, FOXP-1, which were limited in germinal center; Ki-67 was highly expressed in germinal center. CD21 and CD23 showed nodular and expanded follicular dendritic cells. Immunoglobulin gene rearrangement was positive for IGH and IGK. The two patients underwent surgical resection with no complications. After discharge, the two patients with a close review for 18 mo and 5 mo respectively and showed no evidence of recurrence. CONCLUSION: PTFL in adult is generally supposed to be extremely rare. PTFL displayed characteristic morphological, immunophenotypic, and molecular biological changes which are a kind of neoplasm with satisfactory prognosis after surgical excision. Baishideng Publishing Group Inc 2021-11-06 2021-11-06 /pmc/articles/PMC8610869/ /pubmed/34877288 http://dx.doi.org/10.12998/wjcc.v9.i31.9542 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Liu, Yao Xing, Hui Liu, Yue-Ping Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports |
title | Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports |
title_full | Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports |
title_fullStr | Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports |
title_full_unstemmed | Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports |
title_short | Clinical observation of pediatric-type follicular lymphomas in adult: Two case reports |
title_sort | clinical observation of pediatric-type follicular lymphomas in adult: two case reports |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610869/ https://www.ncbi.nlm.nih.gov/pubmed/34877288 http://dx.doi.org/10.12998/wjcc.v9.i31.9542 |
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