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Multicentric Castleman's disease developing during follow‐up of sarcoidosis
Pulmonary sarcoidosis is reported to have complication of lymphoproliferative disease such as malignant lymphoma, but the complication of multicentric Castleman's disease (MCD) is rarely reported. In our case of a 60‐year‐old woman, bilateral hilar lymphadenopathy was noted in her chest X‐ray....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969854/ https://www.ncbi.nlm.nih.gov/pubmed/27512568 http://dx.doi.org/10.1002/rcr2.168 |
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author | Sawata, Tetsuro Bando, Masashi Nakayama, Masayuki Mato, Naoko Takemura, Tamiko Sugiyama, Yukihiko |
author_facet | Sawata, Tetsuro Bando, Masashi Nakayama, Masayuki Mato, Naoko Takemura, Tamiko Sugiyama, Yukihiko |
author_sort | Sawata, Tetsuro |
collection | PubMed |
description | Pulmonary sarcoidosis is reported to have complication of lymphoproliferative disease such as malignant lymphoma, but the complication of multicentric Castleman's disease (MCD) is rarely reported. In our case of a 60‐year‐old woman, bilateral hilar lymphadenopathy was noted in her chest X‐ray. We performed a transbronchial lung biopsy. She was diagnosed as having pulmonary sarcoidosis (Stage II). The shadow on chest X‐ray disappeared without treatment. However, after 8 years, swelling of the mediastinal and abdominal lymph node, thickened bronchovascular bundle, and multiple nodular shadows were identified, and a thoracoscopic lung biopsy was performed. Based on the histopathological findings and elevated serum interleukin‐6 level (75.7 pg/mL), she was diagnosed with pulmonary sarcoidosis complicated by MCD. When a change in chest X‐ray findings are found during monitoring of pulmonary sarcoidosis, it is important to proceed with a thoracoscopic lung biopsy, because of the possibility of the rare complication of MCD. |
format | Online Article Text |
id | pubmed-4969854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49698542016-08-11 Multicentric Castleman's disease developing during follow‐up of sarcoidosis Sawata, Tetsuro Bando, Masashi Nakayama, Masayuki Mato, Naoko Takemura, Tamiko Sugiyama, Yukihiko Respirol Case Rep Case Reports Pulmonary sarcoidosis is reported to have complication of lymphoproliferative disease such as malignant lymphoma, but the complication of multicentric Castleman's disease (MCD) is rarely reported. In our case of a 60‐year‐old woman, bilateral hilar lymphadenopathy was noted in her chest X‐ray. We performed a transbronchial lung biopsy. She was diagnosed as having pulmonary sarcoidosis (Stage II). The shadow on chest X‐ray disappeared without treatment. However, after 8 years, swelling of the mediastinal and abdominal lymph node, thickened bronchovascular bundle, and multiple nodular shadows were identified, and a thoracoscopic lung biopsy was performed. Based on the histopathological findings and elevated serum interleukin‐6 level (75.7 pg/mL), she was diagnosed with pulmonary sarcoidosis complicated by MCD. When a change in chest X‐ray findings are found during monitoring of pulmonary sarcoidosis, it is important to proceed with a thoracoscopic lung biopsy, because of the possibility of the rare complication of MCD. John Wiley and Sons Inc. 2016-05-28 /pmc/articles/PMC4969854/ /pubmed/27512568 http://dx.doi.org/10.1002/rcr2.168 Text en © 2016 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 Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Sawata, Tetsuro Bando, Masashi Nakayama, Masayuki Mato, Naoko Takemura, Tamiko Sugiyama, Yukihiko Multicentric Castleman's disease developing during follow‐up of sarcoidosis |
title | Multicentric Castleman's disease developing during follow‐up of sarcoidosis |
title_full | Multicentric Castleman's disease developing during follow‐up of sarcoidosis |
title_fullStr | Multicentric Castleman's disease developing during follow‐up of sarcoidosis |
title_full_unstemmed | Multicentric Castleman's disease developing during follow‐up of sarcoidosis |
title_short | Multicentric Castleman's disease developing during follow‐up of sarcoidosis |
title_sort | multicentric castleman's disease developing during follow‐up of sarcoidosis |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969854/ https://www.ncbi.nlm.nih.gov/pubmed/27512568 http://dx.doi.org/10.1002/rcr2.168 |
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