{"title":"Differential expression of immunohistochemistry markers for epithelial/squamous cells in adamantinomatous craniopharyngioma","authors":"N. Abu-Farsakh, I. Sbeih, H. Farsakh","doi":"10.15406/ICPJL.2017.05.00122","DOIUrl":null,"url":null,"abstract":"Craniopharyngioma are histologically a benign neoplasm that occurs in the sellar and suprasellar region, with an infiltrative growth pattern, accounts for 1.2-4.6% of all intracranial tumors.1 They are the most common non-neuroepithelial intracerebral neoplasm in children accounting for 5-10% of intracranial tumors in this age group. A bimodal age distribution of ACP is observed, with peaks in children aged 5-15years and adults 45-60years.1 They are often difficult to excise surgically, and they have a 10% to 40% recurrence rate.2 There are at two types of craniopharyngioma: Adamantinomatous craniopharyngioma (ACP) and papillary craniopharyngioma (PCP). Both have distinct morphology and different clinical behavior. ACP has at least four different squamous histological areas: superficial mature squamous (SMS), loosely cohesive aggregates of squamous cells known as “stellate reticulum” (SR), palisaded basal columnar (PBC) cells and nodules of wet keratin (WK) (Figure 1, Figure 2 & Figure 3). Cystic cavities containing squamous debris are lined by flattened epithelium. PCP occurs virtually exclusively in adults with mean age of 40-50years.3,4 Histologically, it is different from ACP by lacking nuclear palisading, wet keratin, and dystrophic calcification.5","PeriodicalId":92215,"journal":{"name":"International clinical pathology journal","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International clinical pathology journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/ICPJL.2017.05.00122","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Craniopharyngioma are histologically a benign neoplasm that occurs in the sellar and suprasellar region, with an infiltrative growth pattern, accounts for 1.2-4.6% of all intracranial tumors.1 They are the most common non-neuroepithelial intracerebral neoplasm in children accounting for 5-10% of intracranial tumors in this age group. A bimodal age distribution of ACP is observed, with peaks in children aged 5-15years and adults 45-60years.1 They are often difficult to excise surgically, and they have a 10% to 40% recurrence rate.2 There are at two types of craniopharyngioma: Adamantinomatous craniopharyngioma (ACP) and papillary craniopharyngioma (PCP). Both have distinct morphology and different clinical behavior. ACP has at least four different squamous histological areas: superficial mature squamous (SMS), loosely cohesive aggregates of squamous cells known as “stellate reticulum” (SR), palisaded basal columnar (PBC) cells and nodules of wet keratin (WK) (Figure 1, Figure 2 & Figure 3). Cystic cavities containing squamous debris are lined by flattened epithelium. PCP occurs virtually exclusively in adults with mean age of 40-50years.3,4 Histologically, it is different from ACP by lacking nuclear palisading, wet keratin, and dystrophic calcification.5