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1.
Annals of Dermatology ; : 331-334, 2018.
Article in English | WPRIM | ID: wpr-715491

ABSTRACT

BACKGROUND: Labial melanotic macules (LMMs) are benign pigmented lesions that usually take the shape of flat asymmetrical macules with tan-brown to black color and variable size. Whereas the dermoscopic features of other pigmented skin lesions have been relatively well described, little is known about LMMs. OBJECTIVE: To describe the dermoscopic features and find typical and schematic dermoscopic patterns in LMMs. METHODS: A retrospective dermoscopic study was conducted on 80 lesions with histopathologically proved LMMs. RESULTS: We described and defined, for the first time to our knowledge, landscape painting patterns found in 65 of 80 melanotic lesions (81.3%), characterized by parallel lines or circle lines, overlapping vessels with background brown pigmentation. The background brown pigmentations were observed in 74 of 80 lesions (92.5%), the parallel lines in 62 (77.5%), the circle lines in 20 (25.0%), and overlapping vessels in 69 (86.3%). The structureless black pigmentations were only presented in 26 of 80 (32.5%). CONCLUSION: Dermoscopy can be useful for the clinical detection of LMMs, and “Landscape painting patterns” may represent a dermoscopic clue for the diagnosis of these lesions.


Subject(s)
Dermoscopy , Diagnosis , Paint , Paintings , Pigmentation , Retrospective Studies , Skin
2.
Journal of Korean Medical Science ; : 273-278, 2000.
Article in English | WPRIM | ID: wpr-132632

ABSTRACT

Atherosclerosis is an inflammatory disease. Platelet-endothelium interaction plays an important role in the pathophysiology of atherogenesis. We investigated the role of activated platelets for secretion of interleukin (IL)-1beta, monocyte chemotactic protein (MCP)-1 and macrophage inflammatory protein (MIP)-1alpha and expression of intercellular adhesion molecule (ICAM)-1 on endothelial cells. Human umbilical vein endothelial cells (HUVEC) were incubated with non-stimulated or ADP-activated platelets for 6 hr. Secretion of interleukin (IL)-1beta, MCP-1 and MIP-1alpha and surface expression of ICAM-1 were measured by ELISA and flow cytometry. In the presence of activated platelets, the secretion of IL-1beta, MCP-1, and MIP-1alpha and surface expression of ICAM-1 were significantly increased compared with non-activated platelets. The present study shows that activated platelets may contribute to expression of various inflammatory mediators on endothelial cells.


Subject(s)
Humans , Blood Platelets/metabolism , Cells, Cultured , Cells, Cultured , Endothelium, Vascular/metabolism , Endothelium, Vascular/cytology , Intercellular Adhesion Molecule-1/biosynthesis , Interleukin-1/metabolism , Macrophage Inflammatory Proteins/metabolism , Chemokine CCL2/metabolism , Platelet Activation/physiology
3.
Journal of Korean Medical Science ; : 273-278, 2000.
Article in English | WPRIM | ID: wpr-132629

ABSTRACT

Atherosclerosis is an inflammatory disease. Platelet-endothelium interaction plays an important role in the pathophysiology of atherogenesis. We investigated the role of activated platelets for secretion of interleukin (IL)-1beta, monocyte chemotactic protein (MCP)-1 and macrophage inflammatory protein (MIP)-1alpha and expression of intercellular adhesion molecule (ICAM)-1 on endothelial cells. Human umbilical vein endothelial cells (HUVEC) were incubated with non-stimulated or ADP-activated platelets for 6 hr. Secretion of interleukin (IL)-1beta, MCP-1 and MIP-1alpha and surface expression of ICAM-1 were measured by ELISA and flow cytometry. In the presence of activated platelets, the secretion of IL-1beta, MCP-1, and MIP-1alpha and surface expression of ICAM-1 were significantly increased compared with non-activated platelets. The present study shows that activated platelets may contribute to expression of various inflammatory mediators on endothelial cells.


Subject(s)
Humans , Blood Platelets/metabolism , Cells, Cultured , Cells, Cultured , Endothelium, Vascular/metabolism , Endothelium, Vascular/cytology , Intercellular Adhesion Molecule-1/biosynthesis , Interleukin-1/metabolism , Macrophage Inflammatory Proteins/metabolism , Chemokine CCL2/metabolism , Platelet Activation/physiology
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