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成釉细胞瘤中的角质形成细胞解离(桥粒溶解/棘层松解)。

Keratinocyte dissociation (desmolysis/acantholysis) in ameloblastoma.

作者信息

Sarode Sachin C, Sarode Gargi S, Birur Praveen, Alhazmi Yaser A, Patil Shankargouda

机构信息

Department of Oral Pathology and Microbiology, Dr. D.Y. Patil Dental College and Hospital, Dr. D.Y. Patil Vidyapeeth, Sant-Tukaram Nagar, Pimpri, Pune, MH, India.

Department of Oral Medicine and Radiology, KLE's Institute of Dental Sciences, Bangalore, India.

出版信息

Clin Pract. 2020 May 19;10(1):1255. doi: 10.4081/cp.2020.1255.

Abstract

Ameloblastoma is the only odontogenic tumor that displays diversified histomorphological features with subtypes like follicular, plexiform, acanthomatous, granular cell, clear cell, desmoplastic etc. In this paper we presented an extremely unusual presentation of ameloblastoma, which is characterized by desmolysis or acantholysis of stellate reticulum-like cells caused due to keratinocyte dissociation. A 35-year-old male patient presented with a painless hard 3×3 cm swelling in the mandibular right posterior region in the past 4-5 months. Radiographic examination revealed a multilocular radiolucent lesion in the body of mandible with resorption of the roots. Histopathological examination revealed ameloblastic follicles with central cells showing keratinocyte dissociation leading to desmolysis/acantholysis. Desmolytic cells were seen as an isolated entity in the follicular space with round to polygonal shaped morphology. Future retrospective studies on archival samples of ameloblastoma are recommended to relook into identification of such rare phenomenon. This will help in better understanding of the incidence rate and biological behavior of this rare variant of ameloblastoma.

摘要

成釉细胞瘤是唯一一种具有多种组织形态学特征的牙源性肿瘤,有滤泡型、丛状型、棘皮瘤型、颗粒细胞型、透明细胞型、促结缔组织增生型等亚型。在本文中,我们展示了成釉细胞瘤一种极其罕见的表现形式,其特征是由于角质形成细胞解离导致星网状样细胞的桥粒溶解或棘层松解。一名35岁男性患者在过去4至5个月中,下颌右后区域出现一个3×3厘米大小无痛性硬性肿胀。影像学检查显示下颌骨体部有一多房性透射性病变,牙根有吸收。组织病理学检查显示成釉细胞滤泡,中央细胞出现角质形成细胞解离,导致桥粒溶解/棘层松解。桥粒溶解细胞在滤泡间隙中表现为孤立的实体,形态为圆形至多边形。建议对成釉细胞瘤存档样本进行未来回顾性研究,以重新审视这种罕见现象的识别。这将有助于更好地了解这种罕见的成釉细胞瘤变体的发病率和生物学行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a512/7282315/9b1d86f13ba2/cp-10-1-1255-g001.jpg

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