Zargaran Massoumeh, Baghaei Fahimeh, Moghimbeigi Abbas, Baghai Fereshteh
Dental Research Center, Department of Oral and Maxillofacial Pathology, School of Dentistry, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Oral and Maxillofacial Pathology, School of Dentistry, Hamadan University of Medical Sciences, Hamadan, Iran.
J Investig Clin Dent. 2019 Nov;10(4):e12451. doi: 10.1111/jicd.12451. Epub 2019 Aug 21.
Despite their histopathological similarity, unlike peripheral giant cell granuloma (PGCG), central giant cell granuloma (CGCG) is an osteolytic lesion. Low motility of osteoclasts as bone-resorbing agents decreases osteolysis where CD44 plays a role. The lesion requires angiogenesis to grow which in turn may cause bone resorption. This study aims to compare CD44 and CD34 expression in PGCG and CGCG.
30 PGCG (group A) and 30 CGCG (group B) including non-aggressive (B1, N = 14) and aggressive (B2, N = 16) subgroups were evaluated for CD44 and CD34 expression through immunohistochemistry.
CD44 staining intensity distribution (SID) score and CD44 labelling index (LI) in PGCG were significantly higher than those in CGCG, while microvessel density assessed by CD34 (MVD-CD34) was significantly higher in CGCG compared with PGCG. CD44-SID score and CD44-LI were higher for B1 whereas MVD-CD34 was higher for B2 (P < .05).
Different CD44 expression among the studied groups may be indicative of the different motility of osteoclastic giant cells which may influence bone resorption. Lower CD44 expression probably indicates higher osteoclastic giant cell motility in CGCG, which with its higher angiogenesis may explain the different clinical behavior of CGCG compared with that of PGCG.
尽管外周巨细胞肉芽肿(PGCG)和中央巨细胞肉芽肿(CGCG)在组织病理学上相似,但CGCG是一种溶骨性病变。作为骨吸收剂的破骨细胞低活性会减少骨溶解,而CD44在其中发挥作用。病变的生长需要血管生成,而血管生成反过来可能导致骨吸收。本研究旨在比较PGCG和CGCG中CD44和CD34的表达。
通过免疫组织化学评估30例PGCG(A组)和30例CGCG(B组),其中B组包括非侵袭性(B1,n = 14)和侵袭性(B2,n = 16)亚组的CD44和CD34表达。
PGCG中CD44染色强度分布(SID)评分和CD44标记指数(LI)显著高于CGCG,而通过CD34评估的微血管密度(MVD-CD34)在CGCG中显著高于PGCG。B1组的CD44-SID评分和CD44-LI较高,而B2组的MVD-CD34较高(P < 0.05)。
研究组之间不同的CD44表达可能表明破骨巨细胞的不同活性,这可能影响骨吸收。较低的CD44表达可能表明CGCG中破骨巨细胞活性较高,其较高的血管生成可能解释了CGCG与PGCG相比不同的临床行为。