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dc.contributor.authorBarbek, B
dc.contributor.authorGorgun, B
dc.contributor.authorAgir, H
dc.contributor.authorKoldas, T
dc.date.accessioned2021-03-05T19:41:50Z
dc.date.available2021-03-05T19:41:50Z
dc.date.issued1997
dc.identifier.citationKoldas T., Barbek B., Agir H., Gorgun B., "Hemangioma of the masseter muscle: report of a case", EUROPEAN JOURNAL OF PLASTIC SURGERY, cilt.20, ss.223-224, 1997
dc.identifier.issn0930-343X
dc.identifier.otherav_d07acaf7-37e9-4b81-9f17-20634d0a58c3
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/137826
dc.identifier.urihttps://doi.org/10.1007/bf01152202
dc.description.abstractThis condition constitutes 0.8% of all hemangiomas, 14% in the head and neck [1]. Skeletal muscle involvement was first described in 1843 by Listen [2]. The rarity of these tumors and the difficulty with diagnosis often leads to incomplete excision [3]. These are congenital lesions consisting of mesodermal nests of vasoformative tissue that gives rise to the vascular tree [4]. They may be exacerbated by trauma and reproductive hormones [3, 5]. They can resolve spontaneously [3, 4, 6]. They present as a palpable, rubbery mass in 98% of cases [4]. Occasionally, they are compressible and pulsate. Conventional X-rays show phleboliths, MRI scanning gives good soft tissue definition, but angiography reveals the vascular nature of the tumor [7]. Irradiation cautery, sclerosants, lasers, steroids and surgical excision have been used for treatment [3, 4, 6, 8, 12]. Total excision is the treatment of choice [4, 6, 10, 13, 14].
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectCERRAHİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectCerrahi Tıp Bilimleri
dc.titleHemangioma of the masseter muscle: report of a case
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF PLASTIC SURGERY
dc.contributor.department, ,
dc.identifier.volume20
dc.identifier.issue4
dc.identifier.startpage223
dc.identifier.endpage224
dc.contributor.firstauthorID119106


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