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Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child

INTRODUCTION: Primary bone lymphomas are rare, and primary anaplastic large cell lymphomas (ALCLs) of bone in a child are even rarer. A case of primary ALCL of calcaneus in a 7-year-old child is presented. CASE REPORT: Child aged 7 years presented with fungating swelling over his right heel which wa...

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Autores principales: Barik, Sitanshu, Goyal, Nikhil, Paul, Souvik, Singh, Vivek, Arora, Shobha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210905/
https://www.ncbi.nlm.nih.gov/pubmed/32405479
http://dx.doi.org/10.13107/jocr.2019.v09.i04.1458
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author Barik, Sitanshu
Goyal, Nikhil
Paul, Souvik
Singh, Vivek
Arora, Shobha
author_facet Barik, Sitanshu
Goyal, Nikhil
Paul, Souvik
Singh, Vivek
Arora, Shobha
author_sort Barik, Sitanshu
collection PubMed
description INTRODUCTION: Primary bone lymphomas are rare, and primary anaplastic large cell lymphomas (ALCLs) of bone in a child are even rarer. A case of primary ALCL of calcaneus in a 7-year-old child is presented. CASE REPORT: Child aged 7 years presented with fungating swelling over his right heel which was associated with fever. The diagnosis was established by immunohistochemistry (CD30, ALK) of the biopsied specimen. Treatment was done by chemotherapy and subsequent radiotherapy. At 12-month follow-up, the child was ambulant with complete resolution of the swelling. CONCLUSION: Masses arising from the foot and ankle can be a diagnostic challenge, and both infection and neoplasm should be considered in its differentials.
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spelling pubmed-72109052020-05-13 Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child Barik, Sitanshu Goyal, Nikhil Paul, Souvik Singh, Vivek Arora, Shobha J Orthop Case Rep Case Report INTRODUCTION: Primary bone lymphomas are rare, and primary anaplastic large cell lymphomas (ALCLs) of bone in a child are even rarer. A case of primary ALCL of calcaneus in a 7-year-old child is presented. CASE REPORT: Child aged 7 years presented with fungating swelling over his right heel which was associated with fever. The diagnosis was established by immunohistochemistry (CD30, ALK) of the biopsied specimen. Treatment was done by chemotherapy and subsequent radiotherapy. At 12-month follow-up, the child was ambulant with complete resolution of the swelling. CONCLUSION: Masses arising from the foot and ankle can be a diagnostic challenge, and both infection and neoplasm should be considered in its differentials. Indian Orthopaedic Research Group 2019 /pmc/articles/PMC7210905/ /pubmed/32405479 http://dx.doi.org/10.13107/jocr.2019.v09.i04.1458 Text en Copyright: © Indian Orthopaedic Research Group http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Barik, Sitanshu
Goyal, Nikhil
Paul, Souvik
Singh, Vivek
Arora, Shobha
Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child
title Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child
title_full Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child
title_fullStr Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child
title_full_unstemmed Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child
title_short Primary Bone Lymphoma: A Rare Case of Anaplastic Large Cell Lymphoma in Calcaneus in a Child
title_sort primary bone lymphoma: a rare case of anaplastic large cell lymphoma in calcaneus in a child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210905/
https://www.ncbi.nlm.nih.gov/pubmed/32405479
http://dx.doi.org/10.13107/jocr.2019.v09.i04.1458
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