DİLDE MASSON HEMANJİOMA

Yıl 2016, Cilt: 18 Sayı: 2, 80 - 82, 31.08.2016

Süheyla Kandemir Gökçe Şimşek Bengi Melikoğlu Mahi Balcı Nuray Bayar Muluk Rahmi Kılıç

https://doi.org/10.24938/kutfd.252682

Öz

İntravasküler papiller endotelyal hiperplazi
(Masson hemanjioma) nadir görülen, normal kan damarları veya vasküler
malformasyonlarda, endotel hücrelerin aşırı proliferasyonunun yol açtığı
vasküler kaynaklı benign bir lezyondur. Anjiosarkom ile karışabilir. Masson
tümörü vücudun herhangi bir bölgesindeki kan damarlarında görülebilir, fakat
çoğunlukla cilt ve ciltaltı dokusunda görülür. Oral kavitede Masson tümörü çok
nadir bir durumdur. Onüç yaşında bayan hasta dilde kitle şikâyeti ile
polikliniğimize başvurdu. Dildeki bu lezyon 1 yıldır mevcuttu. Hastanın oral
muayenesinde dil sağ lateralinde yaklaşık 1x1 cm’lik yüzeyden kabarık, mavi
renkli, yumuşak kıvamda bir kitle görüldü. Total olarak eksize edilen kitlenin,
histopatolojik inceleme sonucu Masson hemanjioma olarak rapor edildi. Bu olguyu
dilde Masson hemanjiomanın nadir görülmesi ve oral kavite kitlelerinin ayırıcı
tanısında düşünülmesi gerektiği nedeniyle sunduk.

Anahtar Kelimeler

Dil, intravasküler papiller endotelyal hiperplazi, Masson tümör

Masson’s Hemangioma of Tongue

Öz

Intravascular
papillary endothelial hyperplasia (Masson's hemangioma) is an unusual benign
vascular lesion, caused by excessive proliferation of endothelial cells in
normal blood vessels or vascular malformations. It can be misdiagnosed with
angiosarcoma. Masson's tumor can be seen in any blood vessel in the body, but
most often occurs in the skin and subcutaneous tissue. Masson tumor in the oral
cavity is a very rare condition. A thirteen-year-old female patient was
admitted to our clinic with the complaint of mass lesion of the tongue. This
lesion of the tongue was present for 1 year. A vegetating, blue colored, soft,
approximately 1x1 cm mass lesion in the right lateral surface of the tongue was
seen in the oral examination of the patient. Mass lesion was excised totally
and histopathologic examination was reported as Masson's hemangioma. In this
case report we presented a rare lesion of Masson's hemangioma which should be
considered in the differential diagnosis of oral cavity masses. 

Anahtar Kelimeler

Intravascular papillary endothelial hyperplasia, Masson tumor, tongue

Kaynakça

• 1. Duong DH, Scoones DJ, Bates D, Sengupta RP. Multiple intracerebra lintravascular papillary endothelial hyperplasia. Acta Neurochir. 1997; 139(9): 883-6.
• 2. Kristof RA, Van Roost D, Wolf HK, Schramm J. Intravascular papillary endothelial hyperplasia of the sellar region. Report of three cases and review of the literature. J Neurosurg. 1997; 86 (3): 558-63.
• 3. Lesley WS, Kupsky WJ, Guthikonda M. İntravascular papillary endothelial hyperplasia arising within a posteroinferior cerebeller artery aneurysm; Case report and review of the literature. Neurosurgery. 2000; 47(4): 961-6.
• 4. Avellino AM, Grant GA, Harris AB, Wallace SK, Shaw CM. Recurrent intracranial Masson's vegetant intravascular hemangioendothelioma. Case report and review of the literature. J Neurosurg. 1999; 91 (2): 308-12.
• 5. Moon WS, Chung GH, Hong KH. Intravascular papillary endothelial hyperplasia in a vascular lesion of the paranasal sinus. Arch Pathol Lab Med. 2000; 124 (8): 1224-7.
• 6. Taricco MA, Vieira JO Jr, Machado AG, Ito FY. Intravascular papillary endothelial hyperplasia causing cauda equinacompression; Case report. Neurosurgery. 1999; 45 (6): 1478-80.
• 7. Wen DY, Hardten DR, Wirtschafter JD, Sung JH, Haines SJ. Elevated intracranial pressure from cerebral venous obstruction by Masson's vegetant intravascular hemangioendothelioma. Case report. J Neurosurg. 1991; 75(5): 787-90.
• 8. Gökten M, Üzen E, Çakalağaoğlu H. IPEH: Bir Olgu ve Ayırıcı Tanı. Turk J Pathol. 1993; 9(1): 75- 7.
• 9. Buchner A, Merrell PW, Carpenter WM, Leider AS. Oral intravasküler papiller endotelyal hiperplazi. J Oral Pathol Med. 1990; 19(9) :419-22.
• 10. Soares AB, Altemani A, Furuse C, et al. Intravascular papillary endothelial hyperplasia: report of 2 cases and immunohistochemical study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2008; 106(5): 708-11