Multiple angiolymphoid hyperplasia with eosinophilia on the right arm showing unusual presentation

2020 ◽  
Vol 33 (6) ◽  
Author(s):  
Erika Tamabuchi ◽  
Taku Fujimura ◽  
Chinbing Lyu ◽  
Setsuya Aiba
Keyword(s):  
Unusual Presentation ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia ◽  
The Right

scholarly journals Angiolymphoid hyperplasia with eosinophilia (epithelioid hemangioma) of the face: An unusual presentation

2011 ◽  
Vol 2 (8) ◽  
pp. 258-260 ◽  
Author(s):  
Mohammed A. Al-Muharraqi ◽  
Mohammed Khalid Faqi ◽  
Fares Uddin ◽  
Karim Ladak ◽  
Abdulla Darwish
Keyword(s):  
Unusual Presentation ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia ◽  
Epithelioid Hemangioma ◽  
The Face

scholarly journals Unusual presentation of angiolymphoid hyperplasia with eosinophilia treated with intralesional and topic corticosteroid combination therapy

2021 ◽  
Vol 13 (2) ◽  
Author(s):  
Giammarco Granieri ◽  
Teresa Oranges ◽  
Salvatore Panduri ◽  
Barbara Loggini ◽  
Agata Janowska ◽  
...  
Keyword(s):  
Combination Therapy ◽  
Female Patient ◽  
Unusual Presentation ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia ◽  
Benign Disorder ◽  
Caucasian Female

Angiolymphoid hyperplasia with eosinophilia (ALHE) is an uncommon angioproliferative benign disorder. A 24- year-old Caucasian female patient presented with multiple itchy reddish pearly nodule.

scholarly journals Angiolymphoid Hyperplasia with Eosinophilia with Clinical Presentation Concerning for Juvenile Temporal Arteritis

2019 ◽  
Vol 6 (1) ◽  
pp. 25-30
Author(s):  
Emily Li ◽  
John Sinard ◽  
Alberto Distefano ◽  
Mahsa Sohrab
Keyword(s):  
Temporal Arteritis ◽  
Pediatric Population ◽  
Excisional Biopsy ◽  
Final Diagnosis ◽  
Unknown Etiology ◽  
Vascular Tumors ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia ◽  
Doppler Ultrasound Imaging ◽  
The Right

A 20-year-old boy presented with a mass superotemporal to the right eyebrow of 1 month’s duration without a history of recent trauma. Complete examination and workup, including laboratory analysis, Doppler ultrasound imaging, and magnetic resonance imaging, suggested a diagnosis of juvenile temporal arteritis. Excisional biopsy and histopathology contradicted the preoperative workup and yielded the final diagnosis of angiolymphoid hyperplasia with eosinophilia, a rare eosinophilic dermatosis of unknown etiology. This case highlights the need for better characterization of temporal vascular tumors in the pediatric population.

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