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Paratesticular cellular angiofibroma: a case report.
Murashima, Takaya; Kida, Kazutaka; Gi, Toshihiro; Hida, Takuya; Fujii, Masato; Nagai, Takahiro; Takamori, Hiroki; Mukai, Shoichiro; Sato, Yuichiro; Kamoto, Toshiyuki.
Afiliação
  • Murashima T; Department of Urology, Faculty of Medicine, Miyazaki University Hospital, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
  • Kida K; Section of Urology, Harasanshin Hospital, Fukuoka, Japan.
  • Gi T; Department of Pathology, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.
  • Hida T; Department of Urology, Faculty of Medicine, Miyazaki University Hospital, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
  • Fujii M; Department of Urology, Faculty of Medicine, Miyazaki University Hospital, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
  • Nagai T; Department of Urology, Faculty of Medicine, Miyazaki University Hospital, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
  • Takamori H; Department of Urology, Faculty of Medicine, Miyazaki University Hospital, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
  • Mukai S; Department of Urology, Faculty of Medicine, Miyazaki University Hospital, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan. syoichiro_mukai@med.miyazaki-u.ac.jp.
  • Sato Y; Department of Diagnostic Pathology, Faculty of Medicine, Miyazaki University Hospital, Miyazaki, Japan.
  • Kamoto T; Department of Urology, Faculty of Medicine, Miyazaki University Hospital, 5200 Kihara, Kiyotake, Miyazaki, 889-1692, Japan.
J Med Case Rep ; 18(1): 170, 2024 Apr 11.
Article em En | MEDLINE | ID: mdl-38600580
ABSTRACT

INTRODUCTION:

Paratesticular cellular angiofibroma is a rare benign mesenchymal tumor. The optimal management is surgical resection due to the difficulty of preoperative accurate diagnosis. CASE PRESENTATION A 51-year-old Japanese male visited our hospital complaining of asymptomatic left scrotal swelling. Physical examination revealed a nontender elastic paratesticular mass (5.5 cm in diameter). Although testicular germ cell tumor was ruled out clinically, the possibility of malignant potential remained for the tumor. Since the patient consented to complete resection, a transinguinal radical orchiectomy was performed. The pathological diagnosis revealed cellular angiofibroma. The patient recovered without perioperative complications, and no apparent recurrence was observed at 5 years after surgery.

CONCLUSION:

The pathological findings were compatible for cellular angiofibroma. The tumor was successfully resected, and no apparent recurrence was observed at 5 years after surgery.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Angiofibroma / Neoplasias Embrionárias de Células Germinativas Limite: Humans / Male / Middle aged Idioma: En Revista: J Med Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Angiofibroma / Neoplasias Embrionárias de Células Germinativas Limite: Humans / Male / Middle aged Idioma: En Revista: J Med Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão País de publicação: Reino Unido