| CASE REPORT |
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| Year : 2008 | Volume
: 53
| Issue : 3 | Page : 144-145 |
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Angiolymphoid hyperplasia with eosinophilia: Atypical appeareance in an older patient
Ozlem Karabudak1, Oktay Taskapan1, Onder Bozdogan2, Bilal Dogan1
1 Department of Dermatology, GATA Teaching Hospital, Tibbiye Street 81327 Kadikoy, Istanbul, Turkey
2 Department of Pathology, Kirikkale University Faculty of Medicine, Istanbul, Turkey
Correspondence Address:
Ozlem Karabudak
GATA Teaching Hospital, Department of Dermatology, Tibbiye Street 81327 Kadikoy, Istanbul
Turkey
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0019-5154.43206
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We describe a 76-year-old man presenting with a chronic, non-healing ulcer of six-year duration on his left zygomatic area. The skin biopsy specimen taken from the lesion, showed increased vascular proliferation, edematous endothelial cells in the dermal blood vessels and perivascular eosinophilic/lymphocytic infiltration. The routine and specific blood tests were unremarkable. On the basis of these features, the patient was diagnosed as having angiolymphoid hyperplasia with eosinophilia (ALHE). We present the case because of its rarity in older people, atypical clinical appearance; and stress the consideration of ALHE in the differential diagnosis of chronic non-healing superficial ulcers confined to face and neck. |
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