Download full-text PDF

Source
http://dx.doi.org/10.1001/jamadermatol.2017.3021DOI Listing

Publication Analysis

Top Keywords

cutaneous pseudolymphoma
4
pseudolymphoma arising
4
arising wolf's
4
wolf's post-herpetic
4
post-herpetic isotopic
4
isotopic response
4
cutaneous
1
arising
1
wolf's
1
post-herpetic
1

Similar Publications

Cutaneous pseudolymphoma successfully treated with intralesional triamcinolone acetonide: A case report.

SAGE Open Med Case Rep

January 2025

Division of Dermatology, Department of Medicine, McMaster University, Hamilton, ON, Canada.

Cutaneous pseudolymphoma refers to a group of skin conditions that simulate lymphoma either clinically and/or histologically. Cutaneous pseudolymphoma is a benign disorder that can often be misdiagnosed and has a wide range of treatment modalities. Currently, there is no gold standard of treatment, and the literature would benefit from more reports on successful and unsuccessful treatments of cutaneous pseudolymphoma.

View Article and Find Full Text PDF
Article Synopsis
  • Cutaneous reactive lymphoid proliferation (CRLP) mimics cutaneous lymphoma, making it essential to differentiate between the two for correct diagnosis and treatment.* -
  • CRLP can be caused by factors like viruses, drugs, or skin trauma, and requires careful evaluation of clinical and histopathological features for accurate diagnosis.* -
  • A case study highlighted CRLP linked to antidepressant and antihypertensive medications, where excision confirmed the diagnosis, showing benign characteristics with no clonality and prompting ongoing monitoring for recurrence.*
View Article and Find Full Text PDF
Article Synopsis
  • Pseudolymphomatous cutaneous angiosarcoma (cAS) is a rare cancer that can be difficult to diagnose due to its similarity to other lymphoid conditions, showcasing notable lymphocyte presence.
  • A unique case involving a 47-year-old woman with systemic sclerosis (SSc) is presented, characterized by facial swelling and specific imaging findings that led to a skin biopsy showing unusual vascular patterns and dense lymphocyte growth.
  • This case highlights the connection between SSc and higher cancer risk, emphasizing the diagnostic challenges of cAS and the need for early detection and comprehensive management strategies.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!