2013
DOI: 10.1002/lary.23883
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Possible participation of acidic pH in bone resorption in middle ear cholesteatoma

Abstract: These results indicate that acid leakage through the cholesteatoma epithelium probably participates in the resorption of the underlying bone structure. The increased permeability of the cholesteatoma epithelium may be explained by a decrease in filaggrin expression.

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Cited by 18 publications
(26 citation statements)
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“…Areas of bone destruction could be seen at the site of rupture of cholesteatoma [54,55]. Hydroxyapatite, an inorganic bone component is highly insoluble under physiologic pH environment, but solubility dramatically increases as the pH is lowered [56].…”
Section: Mechanisms Of Bone Resorption In Cholesteatomamentioning
confidence: 99%
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“…Areas of bone destruction could be seen at the site of rupture of cholesteatoma [54,55]. Hydroxyapatite, an inorganic bone component is highly insoluble under physiologic pH environment, but solubility dramatically increases as the pH is lowered [56].…”
Section: Mechanisms Of Bone Resorption In Cholesteatomamentioning
confidence: 99%
“…Hydroxyapatite, an inorganic bone component is highly insoluble under physiologic pH environment, but solubility dramatically increases as the pH is lowered [56]. Nguyen et al [55] investigated the role of pH in bone resorption in cholesteatoma and found that the pH of keratin debris was acidic and lower than the antrum mucosa. So, they concluded that acidic pH in cholesteatoma may be one of the factors that promote bone erosion by decalcification of the adjacent bony structures [55].…”
Section: Mechanisms Of Bone Resorption In Cholesteatomamentioning
confidence: 99%
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“…It may be a birth defect (congenital cholesteatoma) or acquired cholesteatoma, which is most commonly associated with repeated middle ear chronic inflammation caused by bacteria or viruses [2,3]. …”
mentioning
confidence: 99%
“…Until the middle period of the 20th century, the pressure necrosis theory was believed to explain this phenomenon. Since the 1970s, a number of inflammatory substances, such as interleukin‐1 α , tumour necrosis factor‐ α , interleukin‐6, macrophage colony‐stimulating factor and prostaglandin E2, have been detected in cholesteatoma tissue, and have been presumed to be responsible for bone resorption in this disease . In the 2000s, the mainstream theory posited that the bone resorption mechanism involves osteoclast activation induced by various inflammatory mediators.…”
mentioning
confidence: 99%