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A. Satpathy, C. Moss, F. Raafat and R. Slator, “Spontaneous Regression of a Rare Tumour in a Child: Angiolymphoid Hyperplasia with Eosinophilia of the Hand: Case Report and Review of the Literature,” British Journal of Plastic Surgery, Vol. 58, No. 6, 2005, pp. 865-868. doi:10.1016/j.bjps.2004.11.014

has been cited by the following article:

• TITLE: Angiolymphoid Hyperplasia with Eosinophilia—A Case Report

  AUTHORS: Pankaj Kumar Doloi, Swagata Khanna

  KEYWORDS: Angiolymphoid Hyperplasia with Eosinophilia (ALHE); Epithelioid Haemangioma; Histiocytoid Haemangioma; Kimura’s Disease

  JOURNAL NAME: International Journal of Otolaryngology and Head & Neck Surgery, Vol.1 No.2, August 20, 2012

  ABSTRACT: Angiolymphoid hyperplasia with eosinophilia is a rare, benign vascular tumor affecting principally the head and neck region of young adult females. Microscopic analysis reveals hyperplastic blood vessels lined by a hypertrophic endothelium. An inflammatory infiltrate rich in eosinophils is also present. Etiology of the lesion is unknown. Various treatment modalities have been described. We present a case successfully treated by excision and local steroid infiltration.