Literature DB >> 23161240

Cellular angiofibroma with atypia or sarcomatous transformation - case description with literature review.

Konrad Ptaszyński1, Anna Szumera-Ciećkiewicz, Artur Bartczak.   

Abstract

Cellular angiofibroma (CAF) is a rare, benign, mesenchymal tumor. It was first described by Nucci et al. in 1997 and then in 1998 by Laskin. The tumor occurs predominantly in the vulvo-vaginal or inguino-scrotal region. We present a 71-year-old male, who was referred to the Bielanski Hospital with a three months' history of a slowly growing nodule in the right groin. Gross examination showed a well-circumscribed tumor attached to the spermatic cord and measuring 6 cm in the greatest dimension. Microscopic examination of the tumor showed a spindle cell lesion with a loose, myxoid, partly collagenized stroma with numerous, prominent thick-walled vessels. Scattered atypical cells were present.

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Year:  2012        PMID: 23161240     DOI: 10.5114/pjp.2012.31508

Source DB:  PubMed          Journal:  Pol J Pathol        ISSN: 1233-9687            Impact factor:   1.072


  2 in total

1.  Cellular angiofibroma of the vulva: a poorly known entity, a case report and literature review.

Authors:  Mouna Khmou; Najat Lamalmi; Abderrahmane Malihy; Lamia Rouas; Zaitouna Alhamany
Journal:  BMC Clin Pathol       Date:  2016-06-04

2.  A rare cellular angiofibroma of the epididymis.

Authors:  Qiang Guo; Jian-Dong Zhang; Li Li; Jian-Ping Xie; Ding Ma; Yan-Gang Zhang
Journal:  Asian J Androl       Date:  2018 Jan-Feb       Impact factor: 3.285

  2 in total

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