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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...

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Detalles Bibliográficos
Autores principales: Kamitani, Rei, Matsumoto, Kazuhiro, Fujiwara, Shinnosuke, Akita, Hirotaka, Mikami, Shuji, Kameyama, Kaori, Jinzaki, Masahiro, Oya, Mototsugu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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
Descripción
Sumario: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.