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A long survival case of spinal nephroblastoma in a dog
BACKGROUND: Dogs’ nephroblastoma of the spinal cord is a rare neoplastic disease, with few reports of long-term survival after surgery. We experienced that surgical treatment with postoperative radiation therapy for spinal nephroblastoma in a dog resulted in the long-term survival of 11 years. CASE...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Faculty of Veterinary Medicine
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109834/ https://www.ncbi.nlm.nih.gov/pubmed/35603077 http://dx.doi.org/10.5455/OVJ.2022.v12.i2.5 |
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author | Nakaichi, Munekazu Iseri, Toshie Horikirizono, Hiro Itoh, Harumichi Sunahara, Hiroshi Nemoto, Yuki Itamoto, Kazuhito Tani, Kenji |
author_facet | Nakaichi, Munekazu Iseri, Toshie Horikirizono, Hiro Itoh, Harumichi Sunahara, Hiroshi Nemoto, Yuki Itamoto, Kazuhito Tani, Kenji |
author_sort | Nakaichi, Munekazu |
collection | PubMed |
description | BACKGROUND: Dogs’ nephroblastoma of the spinal cord is a rare neoplastic disease, with few reports of long-term survival after surgery. We experienced that surgical treatment with postoperative radiation therapy for spinal nephroblastoma in a dog resulted in the long-term survival of 11 years. CASE DESCRIPTION: The patient presented to our veterinary hospital because of progressive hindlimb paralysis. Based on diagnostic imaging, she was diagnosed with a thoracolumbar spinal cord tumor and was treated with surgery. The gross tumor tissue was removed after laminectomy, followed by postoperative radiation therapy using orthovoltage equipment. The histopathological features of the surgical specimen were consistent with those of previously reported spinal nephroblastoma, although infrequent mitotic figures were observed. The dog recovered well after treatment and resumed her normal walking condition. No tumor recurrence was observed on periodic follow-up magnetic resonance imaging performed 10 and 21 months after surgery. Imaging evaluation for the gradual development of hindlimb weakness was performed 9 years after surgery; however, no recurrence of tumor tissue was observed, and spondylosis deformans, probably induced after laminectomy, were identified as a possible cause. The dog died of aspiration pneumonia 11 years after surgery, independent of spinal nephroblastoma. CONCLUSION: To date, no clinical cases of canine spinal cord primary nephroblastoma that survived for 11 years after surgery have been reported. This case strongly suggests that providing intensive treatment for canine spinal nephroblastoma is very important. |
format | Online Article Text |
id | pubmed-9109834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Faculty of Veterinary Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-91098342022-05-21 A long survival case of spinal nephroblastoma in a dog Nakaichi, Munekazu Iseri, Toshie Horikirizono, Hiro Itoh, Harumichi Sunahara, Hiroshi Nemoto, Yuki Itamoto, Kazuhito Tani, Kenji Open Vet J Case Report BACKGROUND: Dogs’ nephroblastoma of the spinal cord is a rare neoplastic disease, with few reports of long-term survival after surgery. We experienced that surgical treatment with postoperative radiation therapy for spinal nephroblastoma in a dog resulted in the long-term survival of 11 years. CASE DESCRIPTION: The patient presented to our veterinary hospital because of progressive hindlimb paralysis. Based on diagnostic imaging, she was diagnosed with a thoracolumbar spinal cord tumor and was treated with surgery. The gross tumor tissue was removed after laminectomy, followed by postoperative radiation therapy using orthovoltage equipment. The histopathological features of the surgical specimen were consistent with those of previously reported spinal nephroblastoma, although infrequent mitotic figures were observed. The dog recovered well after treatment and resumed her normal walking condition. No tumor recurrence was observed on periodic follow-up magnetic resonance imaging performed 10 and 21 months after surgery. Imaging evaluation for the gradual development of hindlimb weakness was performed 9 years after surgery; however, no recurrence of tumor tissue was observed, and spondylosis deformans, probably induced after laminectomy, were identified as a possible cause. The dog died of aspiration pneumonia 11 years after surgery, independent of spinal nephroblastoma. CONCLUSION: To date, no clinical cases of canine spinal cord primary nephroblastoma that survived for 11 years after surgery have been reported. This case strongly suggests that providing intensive treatment for canine spinal nephroblastoma is very important. Faculty of Veterinary Medicine 2022 2022-03-19 /pmc/articles/PMC9109834/ /pubmed/35603077 http://dx.doi.org/10.5455/OVJ.2022.v12.i2.5 Text en https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Nakaichi, Munekazu Iseri, Toshie Horikirizono, Hiro Itoh, Harumichi Sunahara, Hiroshi Nemoto, Yuki Itamoto, Kazuhito Tani, Kenji A long survival case of spinal nephroblastoma in a dog |
title | A long survival case of spinal nephroblastoma in a dog |
title_full | A long survival case of spinal nephroblastoma in a dog |
title_fullStr | A long survival case of spinal nephroblastoma in a dog |
title_full_unstemmed | A long survival case of spinal nephroblastoma in a dog |
title_short | A long survival case of spinal nephroblastoma in a dog |
title_sort | long survival case of spinal nephroblastoma in a dog |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109834/ https://www.ncbi.nlm.nih.gov/pubmed/35603077 http://dx.doi.org/10.5455/OVJ.2022.v12.i2.5 |
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