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A Research of Pyogenic Granuloma Genesis Factor With Immunohistochemical Analysis

Authors
Park, Si HyunLee, Jun HoTak, Min SungLee, Hyun JuChoi, Hwan Jun
Issue Date
Nov-2017
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
Epidermal growth factor receptor; estrogen receptor; lobular capillary hemangioma; progesterone receptor; pyogenic granuloma; vascular endothelial growth factor
Citation
Journal of Craniofacial Surgery, v.28, no.8, pp 2068 - 2072
Pages
5
Journal Title
Journal of Craniofacial Surgery
Volume
28
Number
8
Start Page
2068
End Page
2072
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/7077
DOI
10.1097/SCS.0000000000004148
ISSN
1049-2275
1536-3732
Abstract
Pyogenic granuloma (PG) is a type of vascular tumor for which the growth mechanism is poorly understood. Estrogen and progesterone may influence vascular malformations by increasing neovascularization in the lesions. Pregnancy tumor is a term for PG that occurs on the gingival mucosa of pregnant women in response to local irritation or injury. The etiology and pathogenesis of this phenomenon are not fully understood. Hormonal imbalance has been hypothesized to be responsible for the development of gingival hyper-reactive inflammatory responses. Moreover, it has been shown in vitro that the female sex hormone is a potential regulator of the production of several growth factors, such as vascular endothelial growth factor (VEGF), basic fibroblast growth factor, and nerve growth factor, in various cell types. Epidermal growth factor receptor (EGFR) is also involved in a signaling cascade that influences proliferation and other tumor-promoting activities, as well as the responsiveness to chemotherapy. The aim of this study was to examine the relationship between PG pathogenesis and hormone imbalance in 21 patients. All specimens were analyzed by immunohistochemical staining with hematoxylin and eosin for the following hormones: estrogen receptor, progesterone receptor, VEGF, and EGFR. The analysis of the specimens showed that estrogen receptor and EGFR were not associated with PG, while VEGF was statistically related to PG. In addition, there was no significantly difference between sex, tumor location, or pregnancy. There are few studies about correlation between the pathogenesis of PG and sex hormones or growth factors demonstrated via immunohistochemical analysis. The results of this study indicate that estrogen and progesterone do not influence the pathogenesis of PG; however, VEGF may be associated with the pathogenesis of PG.
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