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A case of inguinal cellular angiofibroma
INTRODUCTION: Cellular angiofibroma is a benign mesenchymal tumor that is rare and has a good prognosis. However, preoperative distinction of cellular angiofibroma from malignant tumors is difficult. CASE PRESENTATION: A 77‐year‐old man complained of a left inguinal mass, which was a solid, painless...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292165/ https://www.ncbi.nlm.nih.gov/pubmed/32743474 http://dx.doi.org/10.1002/iju5.12147 |
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author | Kamitani, Rei Matsumoto, Kazuhiro Fujiwara, Shinnosuke Akita, Hirotaka Mikami, Shuji Kameyama, Kaori Jinzaki, Masahiro Oya, Mototsugu |
author_facet | Kamitani, Rei Matsumoto, Kazuhiro Fujiwara, Shinnosuke Akita, Hirotaka Mikami, Shuji Kameyama, Kaori Jinzaki, Masahiro Oya, Mototsugu |
author_sort | Kamitani, Rei |
collection | PubMed |
description | INTRODUCTION: Cellular angiofibroma is a benign mesenchymal tumor that is rare and has a good prognosis. However, preoperative distinction of cellular angiofibroma from malignant tumors is difficult. CASE PRESENTATION: A 77‐year‐old man complained of a left inguinal mass, which was a solid, painless, mobile tumor measuring approximately 40 mm and contacted with the left spermatic cord. Based on his age, the location and imaging findings, a preoperative diagnosis of myxoid liposarcoma was made. The patient underwent left high inguinal orchiectomy with complete resection of the tumor. Histologically and immunohistochemically, the tumor had no feature of malignancy. A postoperative diagnosis of cellular angiofibroma was made. The patient remains free of disease recurrence 12 months after surgery. CONCLUSION: Cellular angiofibroma is a benign but rare tumor, which is sometimes difficult to distinguish from malignant neoplasms. Further studies are needed to accurately preoperatively diagnose this tumor. |
format | Online Article Text |
id | pubmed-7292165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72921652020-07-30 A case of inguinal cellular angiofibroma Kamitani, Rei Matsumoto, Kazuhiro Fujiwara, Shinnosuke Akita, Hirotaka Mikami, Shuji Kameyama, Kaori Jinzaki, Masahiro Oya, Mototsugu IJU Case Rep Case Reports INTRODUCTION: Cellular angiofibroma is a benign mesenchymal tumor that is rare and has a good prognosis. However, preoperative distinction of cellular angiofibroma from malignant tumors is difficult. CASE PRESENTATION: A 77‐year‐old man complained of a left inguinal mass, which was a solid, painless, mobile tumor measuring approximately 40 mm and contacted with the left spermatic cord. Based on his age, the location and imaging findings, a preoperative diagnosis of myxoid liposarcoma was made. The patient underwent left high inguinal orchiectomy with complete resection of the tumor. Histologically and immunohistochemically, the tumor had no feature of malignancy. A postoperative diagnosis of cellular angiofibroma was made. The patient remains free of disease recurrence 12 months after surgery. CONCLUSION: Cellular angiofibroma is a benign but rare tumor, which is sometimes difficult to distinguish from malignant neoplasms. Further studies are needed to accurately preoperatively diagnose this tumor. John Wiley and Sons Inc. 2020-02-20 /pmc/articles/PMC7292165/ /pubmed/32743474 http://dx.doi.org/10.1002/iju5.12147 Text en © 2020 The Authors. IJU Case Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Urological Association. This is an open access article under the terms of the 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 Kamitani, Rei Matsumoto, Kazuhiro Fujiwara, Shinnosuke Akita, Hirotaka Mikami, Shuji Kameyama, Kaori Jinzaki, Masahiro Oya, Mototsugu A case of inguinal cellular angiofibroma |
title | A case of inguinal cellular angiofibroma |
title_full | A case of inguinal cellular angiofibroma |
title_fullStr | A case of inguinal cellular angiofibroma |
title_full_unstemmed | A case of inguinal cellular angiofibroma |
title_short | A case of inguinal cellular angiofibroma |
title_sort | case of inguinal cellular angiofibroma |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7292165/ https://www.ncbi.nlm.nih.gov/pubmed/32743474 http://dx.doi.org/10.1002/iju5.12147 |
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