Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case report

Peripheral T-cell lymphoma accounts for about 10% of all cases of non-Hodgkin’s lymphoma. However, less than 5% of patients with non-Hodgkin’s lymphoma present with hypercalcaemia as the initial symptom, and less than 1% present with primary bone lesions. We herein describe a 76-year-old Chinese man...

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Main Authors: Chen Li, Weiguo Wang, Lingyun Xu, Dingyun Zheng, Miao Zhang, Qin Zhang, Xiaoqian Wu, Yue Yao, Wenyue Huang, Xue Li, Peipei Ying, Xiuxiu Wang, Liu Shang, Yuhu Feng
Format: Article
Language:English
Published: SAGE Publishing 2021-10-01
Series:Journal of International Medical Research
Online Access:https://doi.org/10.1177/03000605211052229
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author Chen Li
Weiguo Wang
Lingyun Xu
Dingyun Zheng
Miao Zhang
Qin Zhang
Xiaoqian Wu
Yue Yao
Wenyue Huang
Xue Li
Peipei Ying
Xiuxiu Wang
Liu Shang
Yuhu Feng
author_facet Chen Li
Weiguo Wang
Lingyun Xu
Dingyun Zheng
Miao Zhang
Qin Zhang
Xiaoqian Wu
Yue Yao
Wenyue Huang
Xue Li
Peipei Ying
Xiuxiu Wang
Liu Shang
Yuhu Feng
author_sort Chen Li
collection DOAJ
description Peripheral T-cell lymphoma accounts for about 10% of all cases of non-Hodgkin’s lymphoma. However, less than 5% of patients with non-Hodgkin’s lymphoma present with hypercalcaemia as the initial symptom, and less than 1% present with primary bone lesions. We herein describe a 76-year-old Chinese man who was diagnosed with primary bone adult T-cell lymphoma with extensive osteolysis, including bone loss in the radius, as the initial manifestation. He had developed severe generalised bone pain and an inability to raise his arms. X-ray examination revealed osteolytic destruction of the forearm with loss of the radial diaphysis. The patient was diagnosed with peripheral T-cell lymphoma based on his immunohistochemical results. He began treatment with the CHOPE chemotherapy regimen, which resulted in significant improvement of his bone pain.
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spelling doaj.art-704a369b53834b3584baf1ef0e0703972022-12-21T22:39:26ZengSAGE PublishingJournal of International Medical Research1473-23002021-10-014910.1177/03000605211052229Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case reportChen LiWeiguo WangLingyun XuDingyun ZhengMiao ZhangQin ZhangXiaoqian WuYue YaoWenyue HuangXue LiPeipei YingXiuxiu WangLiu ShangYuhu FengPeripheral T-cell lymphoma accounts for about 10% of all cases of non-Hodgkin’s lymphoma. However, less than 5% of patients with non-Hodgkin’s lymphoma present with hypercalcaemia as the initial symptom, and less than 1% present with primary bone lesions. We herein describe a 76-year-old Chinese man who was diagnosed with primary bone adult T-cell lymphoma with extensive osteolysis, including bone loss in the radius, as the initial manifestation. He had developed severe generalised bone pain and an inability to raise his arms. X-ray examination revealed osteolytic destruction of the forearm with loss of the radial diaphysis. The patient was diagnosed with peripheral T-cell lymphoma based on his immunohistochemical results. He began treatment with the CHOPE chemotherapy regimen, which resulted in significant improvement of his bone pain.https://doi.org/10.1177/03000605211052229
spellingShingle Chen Li
Weiguo Wang
Lingyun Xu
Dingyun Zheng
Miao Zhang
Qin Zhang
Xiaoqian Wu
Yue Yao
Wenyue Huang
Xue Li
Peipei Ying
Xiuxiu Wang
Liu Shang
Yuhu Feng
Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case report
Journal of International Medical Research
title Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case report
title_full Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case report
title_fullStr Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case report
title_full_unstemmed Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case report
title_short Multiple osteolytic primary peripheral T-cell bone lymphoma: the first case report
title_sort multiple osteolytic primary peripheral t cell bone lymphoma the first case report
url https://doi.org/10.1177/03000605211052229
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