Expression of the endothelial receptor tyrosine kinase Tie2 in lobular capillary hemangioma of the oral mucosa: an immunohistochemical study

J Oral Pathol Med. 2002 Aug;31(7):432-8. doi: 10.1034/j.1600-0714.2002.310708.x.

Abstract

Background: Lobular capillary hemangioma (LCH) usually occurs in the skin or mucous membranes as a rapidly growing red nodule. LCH is one of the most common vascular lesions in the oral mucosa. Tie2 is a novel, human endothelial receptor tyrosine kinase which may play an important role in blood vessel formation. In this study, we investigated its immunohistochemical expression in LCH of the oral mucosa.

Methods: Double immunostaining with anti-CD34 and antialpha smooth muscle actin (SMA) antibodies was performed to characterize the cellular expression of Tie2 in 15 cases of this condition.

Results: We found Tie2 immunoreactivity in the ovoid cells only, which were frequently intermingled with alphaSMA-positive cells, especially in the hypercellular portion of LCH.

Conclusions: These results suggest that the expression of Tie2 in ovoid cells and the interaction between ovoid cells and alphaSMA-positive cells play an important part in the development and progression of LCH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / analysis
  • Adult
  • Aged
  • Antibodies, Monoclonal
  • Antigens, CD34 / analysis
  • Capillaries / metabolism
  • Capillaries / pathology
  • Child
  • Disease Progression
  • Endothelium, Vascular / pathology
  • Female
  • Granuloma, Pyogenic / pathology*
  • Granuloma, Pyogenic / physiopathology
  • Humans
  • Immunoenzyme Techniques
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Mouth Diseases / pathology*
  • Mouth Diseases / physiopathology
  • Mouth Mucosa / blood supply
  • Mouth Mucosa / pathology
  • Muscle, Smooth, Vascular / pathology
  • Neovascularization, Pathologic / pathology
  • Neovascularization, Pathologic / physiopathology
  • Receptor Protein-Tyrosine Kinases / analysis*
  • Receptor, TIE-2

Substances

  • Actins
  • Antibodies, Monoclonal
  • Antigens, CD34
  • Receptor Protein-Tyrosine Kinases
  • Receptor, TIE-2