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Neurofibroma with adenosis in the mammary gland: a case report
BACKGROUND: Neurofibroma of the breast is extremely rare, with only a few reported cases. Here, we report a case of solitary neurofibroma of the breast in a 95-year-old woman. CASE PRESENTATION: A 95-year-old woman presented with a palpable mass in the left breast. Mammography revealed a well-define...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225381/ https://www.ncbi.nlm.nih.gov/pubmed/37246203 http://dx.doi.org/10.1186/s40792-023-01673-0 |
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author | Yamazaki, Hirokazu Koizumi, Kei Watahiki, Mana Takatsuka, Daiki Asano, Yuko Goto, Mana Shiiya, Norihiko Baba, Satoshi |
author_facet | Yamazaki, Hirokazu Koizumi, Kei Watahiki, Mana Takatsuka, Daiki Asano, Yuko Goto, Mana Shiiya, Norihiko Baba, Satoshi |
author_sort | Yamazaki, Hirokazu |
collection | PubMed |
description | BACKGROUND: Neurofibroma of the breast is extremely rare, with only a few reported cases. Here, we report a case of solitary neurofibroma of the breast in a 95-year-old woman. CASE PRESENTATION: A 95-year-old woman presented with a palpable mass in the left breast. Mammography revealed a well-defined mass. A 1.6-cm round mass was found in the lower outer quadrant of the left breast on ultrasonography. The internal echo of the tumor was a mixture of relatively uniform hypoechoic areas with posterior enhancement and heterogeneous hyperechoic areas. She underwent a core needle biopsy. The pathological findings revealed a spindle cell lesion with no malignant findings. At 2 months follow-up, repeat breast ultrasonography showed that the mass had enlarged to be 2.7 cm in size. A repeat core needle biopsy, however, revealed no particularly new information. Because the tumor was growing and a definite diagnosis was not made, lumpectomy was performed. We found bland-spindled cells with shredded-carrot collagen bundles. Immunohistochemical antibody markers (S100, SOX10, and CD34) were positive for the spindle cells. Some of the tumors maintained the bilayer nature of luminal cells and myoepithelial cells, which might be the reason for internal heterogeneity on ultrasound. A histological diagnosis of neurofibroma with adenosis was made. At 6 months follow-up, no recurrent lesions were found. CONCLUSIONS: Ultrasound and pathological images revealed an extremely rare case of neurofibroma combined with adenosis. Tumor resection was performed because it was difficult to make a definitive diagnosis using needle biopsy. Even when a benign tumor is suspected, short-term follow-up is necessary, and if an enlargement is observed, early tumor resection is recommended. |
format | Online Article Text |
id | pubmed-10225381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-102253812023-05-30 Neurofibroma with adenosis in the mammary gland: a case report Yamazaki, Hirokazu Koizumi, Kei Watahiki, Mana Takatsuka, Daiki Asano, Yuko Goto, Mana Shiiya, Norihiko Baba, Satoshi Surg Case Rep Case Report BACKGROUND: Neurofibroma of the breast is extremely rare, with only a few reported cases. Here, we report a case of solitary neurofibroma of the breast in a 95-year-old woman. CASE PRESENTATION: A 95-year-old woman presented with a palpable mass in the left breast. Mammography revealed a well-defined mass. A 1.6-cm round mass was found in the lower outer quadrant of the left breast on ultrasonography. The internal echo of the tumor was a mixture of relatively uniform hypoechoic areas with posterior enhancement and heterogeneous hyperechoic areas. She underwent a core needle biopsy. The pathological findings revealed a spindle cell lesion with no malignant findings. At 2 months follow-up, repeat breast ultrasonography showed that the mass had enlarged to be 2.7 cm in size. A repeat core needle biopsy, however, revealed no particularly new information. Because the tumor was growing and a definite diagnosis was not made, lumpectomy was performed. We found bland-spindled cells with shredded-carrot collagen bundles. Immunohistochemical antibody markers (S100, SOX10, and CD34) were positive for the spindle cells. Some of the tumors maintained the bilayer nature of luminal cells and myoepithelial cells, which might be the reason for internal heterogeneity on ultrasound. A histological diagnosis of neurofibroma with adenosis was made. At 6 months follow-up, no recurrent lesions were found. CONCLUSIONS: Ultrasound and pathological images revealed an extremely rare case of neurofibroma combined with adenosis. Tumor resection was performed because it was difficult to make a definitive diagnosis using needle biopsy. Even when a benign tumor is suspected, short-term follow-up is necessary, and if an enlargement is observed, early tumor resection is recommended. Springer Berlin Heidelberg 2023-05-29 /pmc/articles/PMC10225381/ /pubmed/37246203 http://dx.doi.org/10.1186/s40792-023-01673-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Yamazaki, Hirokazu Koizumi, Kei Watahiki, Mana Takatsuka, Daiki Asano, Yuko Goto, Mana Shiiya, Norihiko Baba, Satoshi Neurofibroma with adenosis in the mammary gland: a case report |
title | Neurofibroma with adenosis in the mammary gland: a case report |
title_full | Neurofibroma with adenosis in the mammary gland: a case report |
title_fullStr | Neurofibroma with adenosis in the mammary gland: a case report |
title_full_unstemmed | Neurofibroma with adenosis in the mammary gland: a case report |
title_short | Neurofibroma with adenosis in the mammary gland: a case report |
title_sort | neurofibroma with adenosis in the mammary gland: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10225381/ https://www.ncbi.nlm.nih.gov/pubmed/37246203 http://dx.doi.org/10.1186/s40792-023-01673-0 |
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