TY - JOUR
T1 - Assessment of Langerhans cells in oral lichen planus by ATPase histochemistry
T2 - A clinicopathologic correlation
AU - Pandey, Arushi
AU - Setty, Suhas
AU - Rao, Raghavendra
AU - Radhakrishnan, Raghu
PY - 2011
Y1 - 2011
N2 - Objective: To assess the distribution pattern of Langerhans cells in oral lichen planus using adenosine triphosphatase (ATPase) histochemistry and to correlate this with the duration of symptoms. Method and Materials: Included were fresh unfixed tissues from previously untreated cases that were clinically and histologically diagnosed as oral lichen planus (n = 18). Healthy oral mucosal tissues were used as controls (n = 5). ATPase activity in the Langerhans cells from the tissue samples was assessed by enzyme histochemistry. Results: The difference in the distribution pattern of Langerhans cells in the superficial and basal half of the epithelium in both the lesional and control tissue was significant (P < .001, Mann-Whitney U test). With an increase in duration of symptoms, the median migration of cells from superficial position to the basal half was significant (P = .001, Kruskal-Wallis test). A negative correlation (Pearson correlation coefficient) was seen between duration of symptoms and migration of cells. Conclusion: The initial increase in the number of Langerhans cells in the lesional tissues compared to controls suggests that these cells are critically required for both the initiation and progression of the mucosal immune response in oral lichen planus. Variation in their number and distribution bear clinical importance as objective assessment of long-standing lesions could be made with reference to treatment planning.
AB - Objective: To assess the distribution pattern of Langerhans cells in oral lichen planus using adenosine triphosphatase (ATPase) histochemistry and to correlate this with the duration of symptoms. Method and Materials: Included were fresh unfixed tissues from previously untreated cases that were clinically and histologically diagnosed as oral lichen planus (n = 18). Healthy oral mucosal tissues were used as controls (n = 5). ATPase activity in the Langerhans cells from the tissue samples was assessed by enzyme histochemistry. Results: The difference in the distribution pattern of Langerhans cells in the superficial and basal half of the epithelium in both the lesional and control tissue was significant (P < .001, Mann-Whitney U test). With an increase in duration of symptoms, the median migration of cells from superficial position to the basal half was significant (P = .001, Kruskal-Wallis test). A negative correlation (Pearson correlation coefficient) was seen between duration of symptoms and migration of cells. Conclusion: The initial increase in the number of Langerhans cells in the lesional tissues compared to controls suggests that these cells are critically required for both the initiation and progression of the mucosal immune response in oral lichen planus. Variation in their number and distribution bear clinical importance as objective assessment of long-standing lesions could be made with reference to treatment planning.
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M3 - Article
C2 - 21465009
AN - SCOPUS:84860422237
SN - 0033-6572
VL - 42
SP - 225
EP - 234
JO - Quintessence International
JF - Quintessence International
IS - 3
ER -