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Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report
INTRODUCTION: and importance - Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign microvascular proliferation. It is clinically characterized by intradermal or subcutaneous papules and/or nodules. Treatment consists mainly of surgery or laser therapy, with a high recurrence rate. Sp...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170072/ https://www.ncbi.nlm.nih.gov/pubmed/34113439 http://dx.doi.org/10.1016/j.amsu.2021.102376 |
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author | Slimani, Yasmine Hali, Fouzia Sid'Ahmed Tolba, Cheikh Marnissi, Farida Chiheb, Soumiya |
author_facet | Slimani, Yasmine Hali, Fouzia Sid'Ahmed Tolba, Cheikh Marnissi, Farida Chiheb, Soumiya |
author_sort | Slimani, Yasmine |
collection | PubMed |
description | INTRODUCTION: and importance - Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign microvascular proliferation. It is clinically characterized by intradermal or subcutaneous papules and/or nodules. Treatment consists mainly of surgery or laser therapy, with a high recurrence rate. Spontaneous regression is rare but possible. CASE PRESENTATION: A 72-year-old man presented for an erythematous plaque on his scalp. Physical examination demonstrated a large angiomatous indurated subcutaneous plaque. The lesion was not pulsatile. The doppler ultrasound revealed no underlying vascular malformation. The biopsy revealed an ALHE. No further treatment was carried out. During the follow-up, the lesion gradually subsided. After one-year follow-up, the lesion had regressed with no sign of recurrence. CLINICAL DISCUSSION: There are different treatment modalities for AHLE management, including surgical excision, cryotherapy and lasers. However, none of these modalities has provided consistent results and recurrence after treatment is common.). Rare instances of spontaneous regression have been reported. CONCLUSION: Given the rarity of cases of spontaneous resolution, ALHE may be considered as a chronic condition, especially since recurrences are frequent. A “wait and see” approach can be proposed in some specific situations. |
format | Online Article Text |
id | pubmed-8170072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81700722021-06-09 Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report Slimani, Yasmine Hali, Fouzia Sid'Ahmed Tolba, Cheikh Marnissi, Farida Chiheb, Soumiya Ann Med Surg (Lond) Case Report INTRODUCTION: and importance - Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare benign microvascular proliferation. It is clinically characterized by intradermal or subcutaneous papules and/or nodules. Treatment consists mainly of surgery or laser therapy, with a high recurrence rate. Spontaneous regression is rare but possible. CASE PRESENTATION: A 72-year-old man presented for an erythematous plaque on his scalp. Physical examination demonstrated a large angiomatous indurated subcutaneous plaque. The lesion was not pulsatile. The doppler ultrasound revealed no underlying vascular malformation. The biopsy revealed an ALHE. No further treatment was carried out. During the follow-up, the lesion gradually subsided. After one-year follow-up, the lesion had regressed with no sign of recurrence. CLINICAL DISCUSSION: There are different treatment modalities for AHLE management, including surgical excision, cryotherapy and lasers. However, none of these modalities has provided consistent results and recurrence after treatment is common.). Rare instances of spontaneous regression have been reported. CONCLUSION: Given the rarity of cases of spontaneous resolution, ALHE may be considered as a chronic condition, especially since recurrences are frequent. A “wait and see” approach can be proposed in some specific situations. Elsevier 2021-05-15 /pmc/articles/PMC8170072/ /pubmed/34113439 http://dx.doi.org/10.1016/j.amsu.2021.102376 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Slimani, Yasmine Hali, Fouzia Sid'Ahmed Tolba, Cheikh Marnissi, Farida Chiheb, Soumiya Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report |
title | Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report |
title_full | Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report |
title_fullStr | Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report |
title_full_unstemmed | Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report |
title_short | Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report |
title_sort | spontaneous regression of angiolymphoid hyperplasia with eosinophilia (ahle): a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170072/ https://www.ncbi.nlm.nih.gov/pubmed/34113439 http://dx.doi.org/10.1016/j.amsu.2021.102376 |
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