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Intrascrotal hibernoma mimicking liposarcoma: A case study

Hibernoma is a rare benign lipomatous tumor derived from brown fat, which is typically found in infants. Specifically, intrascrotal hibernoma is extremely rare with only one case reported to date. We encountered the second case, which was successfully treated with surgical resection without any recu...

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Detalles Bibliográficos
Autores principales: Hayashida, Michikata, Yano, Akihiro, Nagamoto, Shoichi, Sakaguchi, Kazushige, Okaneya, Toshikazu, Urakami, Shinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170945/
https://www.ncbi.nlm.nih.gov/pubmed/32322531
http://dx.doi.org/10.1016/j.eucr.2020.101206
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author Hayashida, Michikata
Yano, Akihiro
Nagamoto, Shoichi
Sakaguchi, Kazushige
Okaneya, Toshikazu
Urakami, Shinji
author_facet Hayashida, Michikata
Yano, Akihiro
Nagamoto, Shoichi
Sakaguchi, Kazushige
Okaneya, Toshikazu
Urakami, Shinji
author_sort Hayashida, Michikata
collection PubMed
description Hibernoma is a rare benign lipomatous tumor derived from brown fat, which is typically found in infants. Specifically, intrascrotal hibernoma is extremely rare with only one case reported to date. We encountered the second case, which was successfully treated with surgical resection without any recurrence at 3 years. The patient was first misdiagnosed with an intrascrotal liposarcoma preoperatively. Preoperative usefulness of imaging modalities to discriminate hibernomas and liposarcomas is limited due to lack of specific features of hibernomas with its rarity. Here, we report a case of intrascrotal hibernoma in addition to a current literature review.
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spelling pubmed-71709452020-04-22 Intrascrotal hibernoma mimicking liposarcoma: A case study Hayashida, Michikata Yano, Akihiro Nagamoto, Shoichi Sakaguchi, Kazushige Okaneya, Toshikazu Urakami, Shinji Urol Case Rep Oncology Hibernoma is a rare benign lipomatous tumor derived from brown fat, which is typically found in infants. Specifically, intrascrotal hibernoma is extremely rare with only one case reported to date. We encountered the second case, which was successfully treated with surgical resection without any recurrence at 3 years. The patient was first misdiagnosed with an intrascrotal liposarcoma preoperatively. Preoperative usefulness of imaging modalities to discriminate hibernomas and liposarcomas is limited due to lack of specific features of hibernomas with its rarity. Here, we report a case of intrascrotal hibernoma in addition to a current literature review. Elsevier 2020-04-15 /pmc/articles/PMC7170945/ /pubmed/32322531 http://dx.doi.org/10.1016/j.eucr.2020.101206 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Hayashida, Michikata
Yano, Akihiro
Nagamoto, Shoichi
Sakaguchi, Kazushige
Okaneya, Toshikazu
Urakami, Shinji
Intrascrotal hibernoma mimicking liposarcoma: A case study
title Intrascrotal hibernoma mimicking liposarcoma: A case study
title_full Intrascrotal hibernoma mimicking liposarcoma: A case study
title_fullStr Intrascrotal hibernoma mimicking liposarcoma: A case study
title_full_unstemmed Intrascrotal hibernoma mimicking liposarcoma: A case study
title_short Intrascrotal hibernoma mimicking liposarcoma: A case study
title_sort intrascrotal hibernoma mimicking liposarcoma: a case study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170945/
https://www.ncbi.nlm.nih.gov/pubmed/32322531
http://dx.doi.org/10.1016/j.eucr.2020.101206
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