The discriminative role of PROX-1 immunohistochemistry between venous malformation and lymphatic malformation of the deep type with no visible diagnostic surface skin lesion

  • Seok Jong Lee
  • , Nam Gyoung Ha
  • , Ho Youn Kim
  • , Jong Min Lee
  • , Sang Yub Lee
  • , Seung Huh
  • , Ji Yoon Kim
  • , Ho Yun Chung

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Venous malformations (VMs) are distinguished from lymphatic malformations (LMs) when specific diagnostic skin lesions are present. In the deep type, this is difficult by clinico-radiologic evaluation alone. We aimed to investigate the usefulness of lymphatic vessel endothelial cell (LEC) markers for the differential diagnosis of the deep VMs and LMs. Methods: A retrospective study was conducted based on the medical records of patients with VMs and LMs who underwent biopsy with both D2-40 and PROX-1 immunohistochemistry. We compared the initial clinico-radiological diagnosis with the final pathological diagnosis and identified which ones showed a difference. Results: From 261 patients who had VMs and LMs, 111 remained after the exclusion of those who showed definite surface diagnostic features. After pathological diagnosis with the expressions of D2-40 and PROX-1, 38 of 111 (34.2%) patients' final diagnoses were changed. Among these 38 cases, diagnosis was not changed by D2-40 positivity alone, but changed by PROX-1 positivity alone (52.6%) or by both (47.4%). The diagnostic changes were more frequent in the deep category (43.7%) than in the superficial category. Conclusions: Identifying the expression of D2-40, and especially PROX-1, in the differential diagnosis of VMs and LMs may provide important treatment guidelines and understanding their natural course.

Original languageEnglish
Pages (from-to)353-359
Number of pages7
JournalJournal of Cutaneous Pathology
Volume51
Issue number5
DOIs
StatePublished - May 2024
Externally publishedYes

Keywords

  • D2-40
  • lymphatic malformation
  • PROX-1
  • venous malformation

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