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Autor(en) / Beteiligte
Titel
Spontaneous regression of angiolymphoid hyperplasia with eosinophilia (AHLE): A case report
Ist Teil von
  • Annals of medicine and surgery, 2021-06, Vol.66, p.102376, Article 102376
Ort / Verlag
England: Elsevier Ltd
Erscheinungsjahr
2021
Link zum Volltext
Quelle
Free E-Journal (出版社公開部分のみ)
Beschreibungen/Notizen
  • 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. 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. 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. 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. •AHLE is a rare benign microvascular proliferation.•Treatment consists of surgery or laser therapy, with a hight recurrence rate.•Spontaneous regression is rare but possible.•We report a case and review the literature of spontaneously regressive ALHE cases.
Sprache
Englisch
Identifikatoren
ISSN: 2049-0801
eISSN: 2049-0801
DOI: 10.1016/j.amsu.2021.102376
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8170072

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