» Articles » PMID: 31936598

First Glance of Molecular Profile of Atypical Cellular Angiofibroma/Cellular Angiofibroma with Sarcomatous Transformation by Next Generation Sequencing

Overview
Specialty Radiology
Date 2020 Jan 16
PMID 31936598
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Cellular angiofibroma is a rare benign mesenchymal neoplasm most commonly occurring in the vulvovaginal region in women and the inguinoscrotal region in men with specific genetic deletion involved in the gene in chromosome 13q14 region. Atypical cellular angiofibroma and cellular angiofibroma with sarcomatous transformation are recently described variants showing worrisome morphological features and strong, diffuse p16 expression. Nevertheless, the molecular profile of these tumor entities is largely unknown. We carried out a next generation sequencing (NGS) study from six cases of atypical cellular angiofibroma and cellular angiofibroma with sarcomatous transformation. We were able to identify oncogenic gene mutations (33%) which may contribute to pathogenesis also resulting in p16 overexpression. In addition, gene alterations generally present were identified. Since it is a recently described and rare entity, the whole molecular signaling pathway is still largely obscured and the analysis of larger cohorts is needed to elucidate this issue.

Citing Articles

Cellular angiofibroma in the retroperitoneal space during pregnancy: A case report.

Abe H, Nakao S, Itagaki H, Hosokawa Y, Shikama A, Tasaka N BMC Womens Health. 2023; 23(1):57.

PMID: 36765343 PMC: 9912601. DOI: 10.1186/s12905-023-02182-w.


Practical Approach to the Diagnosis of the Vulvo-Vaginal Stromal Tumors: An Overview.

Angelico G, Marletta S, Broggi G, Vigneri P, Vecchio G, Salvatorelli L Diagnostics (Basel). 2022; 12(2).

PMID: 35204448 PMC: 8871080. DOI: 10.3390/diagnostics12020357.


Cellular Angiofibroma Presenting as a Subepithelial Rectal Mass.

Bloom J, Jordan E, Baratta V, Zhang X, Saha A, Yavorek G ACG Case Rep J. 2020; 7(11):e00471.

PMID: 33235884 PMC: 7678802. DOI: 10.14309/crj.0000000000000471.


Next-Generation Sequencing in Tumor Diagnosis and Treatment.

de Biase D, Fassan M, Malapelle U Diagnostics (Basel). 2020; 10(11).

PMID: 33212911 PMC: 7698429. DOI: 10.3390/diagnostics10110962.

References
1.
Hameed M, Clarke K, Amer H, Mahmet K, Aisner S . Cellular angiofibroma is genetically similar to spindle cell lipoma: a case report. Cancer Genet Cytogenet. 2007; 177(2):131-4. DOI: 10.1016/j.cancergencyto.2007.05.016. View

2.
Natarajan E, Saeb M, Crum C, Woo S, McKee P, Rheinwald J . Co-expression of p16(INK4A) and laminin 5 gamma2 by microinvasive and superficial squamous cell carcinomas in vivo and by migrating wound and senescent keratinocytes in culture. Am J Pathol. 2003; 163(2):477-91. PMC: 1868206. DOI: 10.1016/s0002-9440(10)63677-2. View

3.
Creytens D, van Gorp J, Savola S, Ferdinande L, Mentzel T, Libbrecht L . Atypical spindle cell lipoma: a clinicopathologic, immunohistochemical, and molecular study emphasizing its relationship to classical spindle cell lipoma. Virchows Arch. 2014; 465(1):97-108. DOI: 10.1007/s00428-014-1568-8. View

4.
Chen E, Fletcher C . Cellular angiofibroma with atypia or sarcomatous transformation: clinicopathologic analysis of 13 cases. Am J Surg Pathol. 2010; 34(5):707-14. DOI: 10.1097/PAS.0b013e3181d74bdb. View

5.
Nucci M, Granter S, Fletcher C . Cellular angiofibroma: a benign neoplasm distinct from angiomyofibroblastoma and spindle cell lipoma. Am J Surg Pathol. 1997; 21(6):636-44. DOI: 10.1097/00000478-199706000-00002. View