Literature DB >> 12174078

Angiolymphoid hyperplasia with eosinophilia: a classic clinical presentation with histologic features of angiosarcoma.

Nathalie C Zeitouni1, Sameh Hanna, Thom R Loree, John Brooks, Richard T Cheney.   

Abstract

BACKGROUND: Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare disease manifested by the proliferation of morphologically distinct endothelial cells.
OBJECTIVE: To illustrate by a case report the clinical and varied histopathologic findings of ALHE.
METHODS: A 29-year-old woman presented with a clinical picture of ALHE but had several histologic features of angiosarcoma.
RESULTS: Management of this patient included repeat biopsies of the lesions, excision of the involved areas, careful histologic examination of the entire specimen, and appropriate follow-up.
CONCLUSION: ALHE may present with various histologic features. Knowledge of the spectrum of benign and malignant vascular neoplasms helps manage these challenging cases.

Entities:  

Mesh:

Year:  2002        PMID: 12174078     DOI: 10.1046/j.1524-4725.2002.02006.x

Source DB:  PubMed          Journal:  Dermatol Surg        ISSN: 1076-0512            Impact factor:   3.398


  4 in total

1.  Angiolymphoid hyperplasia with eosinophilia - A case report.

Authors:  Joe Jacob; Shibu George; B R Suchit Roy; S N Dildeepa
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2006-07

2.  A Case of Angiolymphoid Hyperplasia with Eosinophilia of the Lower Eyelid.

Authors:  Joung-Sun Lee; Jee-Bum Lee; Seong-Jin Kim; Seung-Chul Lee; Young Ho Won; Sook Jung Yun
Journal:  Ann Dermatol       Date:  2008-09-30       Impact factor: 1.444

Review 3.  Angiolymphoid Hyperplasia with Eosinophilia of the Orbit and Adnexa.

Authors:  Bipasha Mukherjee; Jayant Kadaskar; Omega Priyadarshini; Subramanian Krishnakumar; Jyotirmay Biswas
Journal:  Ocul Oncol Pathol       Date:  2015-07-16

4.  Eosinophilic and neutrophilic leukemoid reaction in a woman with spindle cell sarcoma: a case report.

Authors:  Michael C Snyder; Carl B Lauter
Journal:  J Med Case Rep       Date:  2010-10-21
  4 in total

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