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Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case
A 57‐year‐old man with neurofibromatosis type 1 (NF‐1) and intrathoracic meningoceles was admitted to hospital after presenting with neck pain and progressive dyspnoea. On admission, a chest computed tomography scan demonstrated right pleural effusion, neck tumour, intrathoracic meningoceles, and ri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635143/ https://www.ncbi.nlm.nih.gov/pubmed/31346470 http://dx.doi.org/10.1002/rcr2.463 |
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author | Furukawa, Marie Ota, Hiroki Nakamura, Yasuhiko Nihonyanagi, Yasuhiro Tochigi, Naobumi Homma, Sakae |
author_facet | Furukawa, Marie Ota, Hiroki Nakamura, Yasuhiko Nihonyanagi, Yasuhiro Tochigi, Naobumi Homma, Sakae |
author_sort | Furukawa, Marie |
collection | PubMed |
description | A 57‐year‐old man with neurofibromatosis type 1 (NF‐1) and intrathoracic meningoceles was admitted to hospital after presenting with neck pain and progressive dyspnoea. On admission, a chest computed tomography scan demonstrated right pleural effusion, neck tumour, intrathoracic meningoceles, and rib metastasis. The myelography showed no transportation between the intrathoracic meningoceles and pleural cavity. As a result, these radiological finding indicated the potential for malignant transformation. The appearance of the right pleural effusion was bloody and had no malignant cells. We biopsied the neck tumour, and the tissue showed glass‐like materials but no malignant cells. At 1 month after admission, he developed bladder–rectal disorder, syndrome of inappropriate secretion of antidiuretic hormone, and paralysis of both legs and later died. An autopsy demonstrated glass‐like material in the neck tumour, which was surrounded by malignant cells. NF‐1 appears to have progressed to a malignant peripheral nerve sheath tumour in this patient. |
format | Online Article Text |
id | pubmed-6635143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-66351432019-07-25 Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case Furukawa, Marie Ota, Hiroki Nakamura, Yasuhiko Nihonyanagi, Yasuhiro Tochigi, Naobumi Homma, Sakae Respirol Case Rep Case Reports A 57‐year‐old man with neurofibromatosis type 1 (NF‐1) and intrathoracic meningoceles was admitted to hospital after presenting with neck pain and progressive dyspnoea. On admission, a chest computed tomography scan demonstrated right pleural effusion, neck tumour, intrathoracic meningoceles, and rib metastasis. The myelography showed no transportation between the intrathoracic meningoceles and pleural cavity. As a result, these radiological finding indicated the potential for malignant transformation. The appearance of the right pleural effusion was bloody and had no malignant cells. We biopsied the neck tumour, and the tissue showed glass‐like materials but no malignant cells. At 1 month after admission, he developed bladder–rectal disorder, syndrome of inappropriate secretion of antidiuretic hormone, and paralysis of both legs and later died. An autopsy demonstrated glass‐like material in the neck tumour, which was surrounded by malignant cells. NF‐1 appears to have progressed to a malignant peripheral nerve sheath tumour in this patient. John Wiley & Sons, Ltd 2019-07-16 /pmc/articles/PMC6635143/ /pubmed/31346470 http://dx.doi.org/10.1002/rcr2.463 Text en © 2019 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Furukawa, Marie Ota, Hiroki Nakamura, Yasuhiko Nihonyanagi, Yasuhiro Tochigi, Naobumi Homma, Sakae Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case |
title | Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case |
title_full | Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case |
title_fullStr | Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case |
title_full_unstemmed | Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case |
title_short | Neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case |
title_sort | neurofibromatosis type 1‐associated malignant peripheral nerve sheath tumour carcinomatous pleurisy: an autopsy case |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635143/ https://www.ncbi.nlm.nih.gov/pubmed/31346470 http://dx.doi.org/10.1002/rcr2.463 |
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