Epithelioid hemangioendothelioma: A rarely seen liver tumor

We aimed to present a 25-year-old female patient diagnosed with epithelioid hemangioendothelioma after evaluation who admitted with complaints of diarrhea.

📌 3 Key Takeaways

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Objective & Hypothesis:Epithelioid hemangioendothelioma is a rarely seen borderline tumor that consists of endothelial, epithelioid and dendritic cells.

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Key Findings & Data:Epithelioid hemangioendothelioma is a rarely seen borderline tumor that consists of endothelial, epithelioid and dendritic cells.

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Conclusion & Impact:We aimed to present a 25-year-old female patient diagnosed with epithelioid hemangioendothelioma after evaluation who admitted with complaints of diarrhea.

🔬Design:Research Article

📍Scope:Comprehensive Sample

⚙️Variables:Epiteloid hemanjioendotelioma · karaciğer · ishal

Abstract

Epithelioid hemangioendothelioma is a rarely seen borderline tumor that consists of endothelial, epithelioid and dendritic cells. We aimed to present a 25-year-old female patient diagnosed with epithelioid hemangioendothelioma after evaluation who admitted with complaints of diarrhea.

Özet

Epiteloid hemanjioendotelioma, endotelial, epiteloid ve dendritik hücrelerden oluşan ve nadir görülen borderline bir tümördür. Burada ishal şikayeti ile başvurup epiteloid hemanjioendotelyoma tanısı alan 25 yaşında kadın hasta sunulmuştur.

Keywords

Epiteloid hemanjioendotelioma karaciğer ishal Epithelioid hemangioendothelioma liver diarrhea

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Cite This Article

SEZİKLİ, M., AKKAN, Z. Ç., ŞİRİN, G., TEMİZ, S., BULUN, F., EROĞLU, D. (2014). Epithelioid hemangioendothelioma: A rarely seen liver tumor. Akademik Gastroenteroloji Dergisi, Cilt: 13 - Sayı: 1, 31–33. https://ajindex.com/articles/219148

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References (11)

Weiss ZW, Enzinger FM. Epithelioid hemangioendothelioma; a vascu- lar tumor often mistaken for a carcinoma. Cancer 1982; 50:970-81.
Ishak KG, Sesterhenn IA, Goodman ZD, et al. Epithelioid hemangio- endothelioma of the liver: a clinicopathologic and follow-up study of 32 cases. Hum pathol 1984; 15:839-52.
Mehrabi A, Kashfi A, Fonouni H, et al. Primary malignant hepatic epithelioid hemangioendothelioma: a comprehensive review of the literature with emphasis on the surgical therapy. Cancer 2006; 107:2108-21. Harada J1, Yoshida H, Ueda J, et al. malignant hepatic epithelioid hemangioendothelioma with abdominal pain due to rapid progres- sion. J Nippon Med Sch 2011; 78:246-51.
Sangro B, Iñarrairaegui M, Fernández-Ros N. Malignant epithe- loid hemangioendothelioma of the liver successfully treated with sorafenib. Rare Tumors 2012; 4:e34. Mehrabi A, Kashfi A, Fonouni H, et al. Primary malignant hepatic hemangioendothelioma. A comprehensive review of the literature with emphasis on the surgical therapy. Cancer 2006; 107:2108-21.
Makhlouf HR, Ishak KG, Goodman ZD. Epithelioid hemangioendo- thelioma of the liver; a clinicopatholohic study of 137 cases. Cancer 1999; 85:562-82.
Caruso S, Miraglia R, Maruzelli L, et al. An unusual presentation of malignant hepatic epithelioid hemangioendothelioma with left pleu- ral and pulmonary localization. Pediatr Radiol 2008; 38:1027-30.
Ji ZF, Shen XZ, Zhang DY, et al. Hepatic epithelioid hemangioendothelioma:a report of six patients. J Dig Dis 2010; 11:254-8.
Prokop M, Galanski M. Spiral and multislice computed tomography of the body. 1st edition. New York, Thieme. 2003; 639-81.
Hsieh MS, Liang PC, Kao YC, Shun CT. Hepatic epithelioid heman- gioendothelioma in Taiwan: a single institution over a 15-year pe- riod. J Formos Med Assoc 2010; 109:219-27.
Thin LW, Wong DD, De Boer BW, et al. Hepatic epithelioid heman- gioendothelioma: challenges in diagnosis and management. Intern Med J 2010; 40:710-5.
Langrehr JM, Petersen I, Pfitzmann R, Lopez-Hänninen E. Malig- nant epithelioid hemangioendothelioma of the liver. Results of sur- gical treatment strategies. Chirurg 2005; 76:1161-7.