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An extragonadal germ cell tumor with dermatomyositis: A case report and literature review

The risk of malignancy in inflammatory myopathy patients is well recognized. However, the incidence of germ cell tumor (GCT) with inflammatory myopathy is low, and most reported cases of GCT also exhibit testicular tumors. Therefore, a case of extragonadal GCT with dermatomyositis (DM) is reported i...

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Autores principales: Fujiwara, Yu, Fukuda, Naoki, Ohmoto, Akihiro, Nakano, Kenji, Ono, Makiko, Taira, Shinichiro, Torii, Junichi, Takamatsu, Manabu, Takahashi, Shunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484733/
https://www.ncbi.nlm.nih.gov/pubmed/32953114
http://dx.doi.org/10.3892/mco.2020.2130
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author Fujiwara, Yu
Fukuda, Naoki
Ohmoto, Akihiro
Nakano, Kenji
Ono, Makiko
Taira, Shinichiro
Torii, Junichi
Takamatsu, Manabu
Takahashi, Shunji
author_facet Fujiwara, Yu
Fukuda, Naoki
Ohmoto, Akihiro
Nakano, Kenji
Ono, Makiko
Taira, Shinichiro
Torii, Junichi
Takamatsu, Manabu
Takahashi, Shunji
author_sort Fujiwara, Yu
collection PubMed
description The risk of malignancy in inflammatory myopathy patients is well recognized. However, the incidence of germ cell tumor (GCT) with inflammatory myopathy is low, and most reported cases of GCT also exhibit testicular tumors. Therefore, a case of extragonadal GCT with dermatomyositis (DM) is reported in the current study to better understand this paraneoplastic syndrome. A 53-year-old man presented with bilateral cervical lymph node enlargement. A lymph node biopsy showed embryonal carcinoma, and computed tomography showed multiple lymph node and lung metastases. A period of one month after bleomycin, etoposide and cisplatin (BEP) chemotherapy, this patient developed an erythematous eruption over the extensor surfaces of bilateral fingers, or Gottron's sign and facial erythema. The patient was diagnosed with DM with a positive anti-TIF-1γ-antibody result. High-dose prednisolone was effective, and there has been no evidence of cancer recurrence for over one year. The literature review identified 17 cases of GCT with inflammatory myopathy that have been reported so far, and it was indicated that this is the first case of extragonadal GCT with DM following chemotherapy. This case highlights the importance of monitoring after the completion of cancer treatment, as distinctive dermal and muscular symptoms should cause us to consider the possibility of paraneoplastic inflammatory myopathy.
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spelling pubmed-74847332020-09-18 An extragonadal germ cell tumor with dermatomyositis: A case report and literature review Fujiwara, Yu Fukuda, Naoki Ohmoto, Akihiro Nakano, Kenji Ono, Makiko Taira, Shinichiro Torii, Junichi Takamatsu, Manabu Takahashi, Shunji Mol Clin Oncol Articles The risk of malignancy in inflammatory myopathy patients is well recognized. However, the incidence of germ cell tumor (GCT) with inflammatory myopathy is low, and most reported cases of GCT also exhibit testicular tumors. Therefore, a case of extragonadal GCT with dermatomyositis (DM) is reported in the current study to better understand this paraneoplastic syndrome. A 53-year-old man presented with bilateral cervical lymph node enlargement. A lymph node biopsy showed embryonal carcinoma, and computed tomography showed multiple lymph node and lung metastases. A period of one month after bleomycin, etoposide and cisplatin (BEP) chemotherapy, this patient developed an erythematous eruption over the extensor surfaces of bilateral fingers, or Gottron's sign and facial erythema. The patient was diagnosed with DM with a positive anti-TIF-1γ-antibody result. High-dose prednisolone was effective, and there has been no evidence of cancer recurrence for over one year. The literature review identified 17 cases of GCT with inflammatory myopathy that have been reported so far, and it was indicated that this is the first case of extragonadal GCT with DM following chemotherapy. This case highlights the importance of monitoring after the completion of cancer treatment, as distinctive dermal and muscular symptoms should cause us to consider the possibility of paraneoplastic inflammatory myopathy. D.A. Spandidos 2020-11 2020-09-03 /pmc/articles/PMC7484733/ /pubmed/32953114 http://dx.doi.org/10.3892/mco.2020.2130 Text en Copyright: © Fujiwara et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 Articles
Fujiwara, Yu
Fukuda, Naoki
Ohmoto, Akihiro
Nakano, Kenji
Ono, Makiko
Taira, Shinichiro
Torii, Junichi
Takamatsu, Manabu
Takahashi, Shunji
An extragonadal germ cell tumor with dermatomyositis: A case report and literature review
title An extragonadal germ cell tumor with dermatomyositis: A case report and literature review
title_full An extragonadal germ cell tumor with dermatomyositis: A case report and literature review
title_fullStr An extragonadal germ cell tumor with dermatomyositis: A case report and literature review
title_full_unstemmed An extragonadal germ cell tumor with dermatomyositis: A case report and literature review
title_short An extragonadal germ cell tumor with dermatomyositis: A case report and literature review
title_sort extragonadal germ cell tumor with dermatomyositis: a case report and literature review
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484733/
https://www.ncbi.nlm.nih.gov/pubmed/32953114
http://dx.doi.org/10.3892/mco.2020.2130
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