scholarly journals Epithelioid hemangioma (Angiolymphoid hyperplasia with eosinophilia) in zosteriform distribution

2012 ◽  
Vol 57 (5) ◽  
pp. 401 ◽  
Author(s):  
Yuichi Kurihara ◽  
Hiroyoshi Inoue ◽  
Hiromaro Kiryu ◽  
Masutaka Furue
2007 ◽  
Vol 1 (1) ◽  
Author(s):  
Bruno F Fernandes ◽  
Abdullah Al-Mujaini ◽  
Tina Petrogiannis-Haliotis ◽  
Abdullah Al-Kandari ◽  
Bryan Arthurs ◽  
...  

2009 ◽  
Vol 37 (10) ◽  
pp. 1045-1052 ◽  
Author(s):  
Elaine Cham ◽  
Bruce R. Smoller ◽  
David A. Lorber ◽  
Thomas A. Victor ◽  
Thomas L. Cibull

2011 ◽  
Vol 2 (8) ◽  
pp. 258-260 ◽  
Author(s):  
Mohammed A. Al-Muharraqi ◽  
Mohammed Khalid Faqi ◽  
Fares Uddin ◽  
Karim Ladak ◽  
Abdulla Darwish

2018 ◽  
Vol 45 (6) ◽  
pp. 395-402 ◽  
Author(s):  
Ana Ortins-Pina ◽  
Mar Llamas-Velasco ◽  
Sara Turpin ◽  
Luís Soares-de-Almeida ◽  
Paulo Filipe ◽  
...  

Author(s):  
Margarita Sánchez-Orgaz ◽  
Alfredo Insausti-García ◽  
Laura Yébenes Gregorio ◽  
Alvaro Arbizu Duralde ◽  
Ricardo Romero-Martín

2015 ◽  
Vol 139 (5) ◽  
pp. 683-686 ◽  
Author(s):  
Ruifeng Guo ◽  
Alde Carlo P. Gavino

Angiolymphoid hyperplasia with eosinophilia (ALHE), also named epithelioid hemangioma (EH), is an inflamed vascular tumefaction of uncertain pathogenesis, characterized by proliferation of histiocytoid endothelial cells with prominent lymphocytic and eosinophilic infiltration. Although considered a benign condition, it may recur in up to one-third of cases in the absence of complete surgical excision. The pathogenesis of ALHE/EH is still controversial. However, reaction to trauma and arteriovenous shunting are considered relevant. Histologically, ALHE/EH may be differentiated from other vascular neoplasms by its several unique characteristics including prominent proliferation of plump endothelial cells, and accompanying eosinophilic and lymphocytic inflammation, often with formation of lymphoid follicles. Surgery is the mainstay of treatment and various other treatment strategies have been used with varying results.


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