Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Slimani, Yasmine, Hali, Fouzia, Sid'Ahmed Tolba, Cheikh, Marnissi, Farida, Chiheb, Soumiya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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
_version_ 1783702159610609664
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
work_keys_str_mv AT slimaniyasmine spontaneousregressionofangiolymphoidhyperplasiawitheosinophiliaahleacasereport
AT halifouzia spontaneousregressionofangiolymphoidhyperplasiawitheosinophiliaahleacasereport
AT sidahmedtolbacheikh spontaneousregressionofangiolymphoidhyperplasiawitheosinophiliaahleacasereport
AT marnissifarida spontaneousregressionofangiolymphoidhyperplasiawitheosinophiliaahleacasereport
AT chihebsoumiya spontaneousregressionofangiolymphoidhyperplasiawitheosinophiliaahleacasereport