KaydedilenlerDerginizi ekleyin

Dergiler / Turkish Neurosurgery / 2020 / Cilt: 30 - Sayı: 2

Composite Hemangioendothelioma Settled in the Paraspinal Region: A Rare Case Report

Şevki GÖK
Mehmet Zafer BERKMAN
Eyup BAYKARA
Sayfa
299–302
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

This is a rare case of CHE that hadsettled in the paraspinal region.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Composite hemangioendothelioma (CHE) is a very rare, low-grade malignant vascular tumor.
📊
Temel Bulgular & Veri:The age of onset is usuallybetween 21 and 72 years, with an average age of 39.5-41 years.
💡
Sonuç & Katkı:This is a rare case of CHE that hadsettled in the paraspinal region.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Composite hemangioendothelioma (CHE) is a very rare, low-grade malignant vascular tumor. It is most commonly seen as one ormore nodules on both sides of the fingers and toes. This tumor rarely settles in the paraspinal muscles. The age of onset is usuallybetween 21 and 72 years, with an average age of 39.5-41 years. Treatment is with gross total removal of the lesion. We present acase of a 54-year-old male patient with a 2-year history of low back pain. Lumbar spine magnetic resonance imaging revealed CHEin the right paravertebral muscle in the posterior vicinity of the transverse process between the right paraspinal muscle planes. Theentire mass was removed grossly. The definitive diagnosis of CHE was made histopathologically. This is a rare case of CHE that hadsettled in the paraspinal region.

🔖

Bu Makaleye Atıf Yap

GÖK, Ş., BERKMAN, M. Z., BAYKARA, E. (2020). Composite Hemangioendothelioma Settled in the Paraspinal Region: A Rare Case Report. Turkish Neurosurgery, Cilt: 30 - Sayı: 2, 299–302. https://ajindex.com/articles/399191

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (1)

  1. Amo Y, Masuzawa M, Hamada Y, Katsuoka K: Expression of vascular endothelial growth factor in a human hemangiosarcoma cell line (ISO-HAS). Arch Dermatol Res 293: 296-301, 2001 2. Arbelaez A, Castillo M, Williams L, Armao DM: Vertebral hemangioendothelial sarcoma: MR findings. J Comput Assist Tomogr 23: 981-983, 1999 3. Aydingoz IE, Demirkesen C, Serdar ZA, Mansur AT, Yasar S, Aslan C: Composite haemangioendothelioma with lymphnode metastasis: An unusual presentation at an uncommon site. Clin Exp Dermatol 34: 802-806, 2009 4. Biagioli M, Sbano P, Miracco C, Fimiani M: Composite cutaneous hemangioendothelioma: Case report and review of the literature. Clin Exp Dermatol 30: 385-387, 2005 5. Chaudhuri B, Ronan SG, Manaligod JR: Angiosarcoma arising in a plexiform neurofibroma: A case report. Cancer 46:605- 610, 1980 6. Chu YC, Choi SJ, Park IS, Kim L, Han JY, Kim JM: Composite hemangioendothelioma. Korean J Pathol 40:142-147, 2006 7. Damiani S, Corti B, Neri F, Collina G, Bertoni F: Primary angiosarcoma of the parotid gland arising from benign congenital hemangioma. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 96: 66-69, 2003 8. Fasolis M, Iaquinta C, Montesco MC, Garzino‐Demo P, Tosco P, Tanteri G, Bonandini E, Ninfo V, Berrone S: Composite hemangioendothelioma of the oral cavity: Case report and review of the literature. Head Neck 30: 974-979, 2008 9. Fukunaga M, Suzuki K, Saegusa N, Folpe AL: Composite hemangioendothelioma: Report of 5 cases including one with associated Maffucci syndrome. Am J Surg Pathol 31: 1567- 1572, 2007 10. Mandahl N, Jin YS, Heim S, Willén H, Wennerberg J, Biörklund A, Mitelman F: Trisomy 5 and loss of the Y chromosome as the sole cytogenetic anomalies in a cavernous hemangioma/ angiosarcoma. Genes Chromosomes Cancer 1:315-316, 1990 11. Mentzel T: Hemangioendotheliomas-evolution of a concept of a heterogeneous group of vascular neoplasms. Verh Dtsch Ges Pathol 82:99-111, 1998 (In German) 12. Nayler SJ, Rubin BP, Calonje E, Chan JK, Fletcher CD: Composite hemangioendothelioma: A complex, low-grade vascular lesion mimicking angiosarcoma. Am J Surg Pathol 24: 352-361, 2000 13. Reis-Filho JS, Paiva ME, Lopes JM: Congenital composite hemangioendothelioma: Case report and reappraisal of the hemangioendothelioma spectrum. J Cutan Pathol 29:226- 231, 2002 14. Roncaroli F, Scheithauer BW, Papazoglou S: Primary polymorphous hemangioendothelioma of the spinal cord. J Neurosurg 95 Suppl 1: 93-95, 2001 15. Rossi S, Fletcher CD: Angiosarcom