Literature DB >> 30119962

[A cutaneous case of angiolymphoid hyperplasia with eosinophilia: Presentation of a rare entity].

Arnault Tauziède-Espariat1, Johnny Raffoul2, Shan Rong Sun2, Catherine Lassabe2, Christine Monnin2.   

Abstract

We report the case of a Caucasian 73-year-old woman, without medical history, who is operated of two lesions of the forehead and the scalp measuring 0.4 and 1cm. There is no adenopathy. Histopathological examination revealed a diffuse vascular proliferation of the dermis and the hypodermis composed of small vessels bordered of plump "epthelioid" endothelial cells. There is no mitotic figure. The stroma is slightly fibrous accompanied by a polymorphic inflammatory infiltrate rich in lymphocytes, sometimes arranged in lymphoid follicles, plasma cells and eosinophils. The proposed diagnosis is angiolymphoid hyperplasia with eosinophilia. This is a rare vascular tumor, benign according with the OMS classification and preferentially observed in the skin. We report a cutaneous case, clinical and histopathological data of the reported cases and present the main differential diagnoses.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Angiolymphoid hyperplasia; Eosinophils; Hyperplasie angiolymphoïde; Éosinophiles

Mesh:

Year:  2018        PMID: 30119962     DOI: 10.1016/j.annpat.2018.06.002

Source DB:  PubMed          Journal:  Ann Pathol        ISSN: 0242-6498            Impact factor:   0.407


  1 in total

1.  Angiolymphoid Hyperplasia with Eosinophilia with Clinical Presentation Concerning for Juvenile Temporal Arteritis.

Authors:  Emily Li; John Sinard; Alberto Distefano; Mahsa Sohrab
Journal:  Ocul Oncol Pathol       Date:  2019-06-28
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.