- Tongue Growth during Prenatal Development in Korean Fetuses and Embryos
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Soo Jeong Hong, Bong Geun Cha, Yeon Sook Kim, Suk Keun Lee, Je Geun Chi
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J Pathol Transl Med. 2015;49(6):497-510. Published online October 16, 2015
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DOI: https://doi.org/10.4132/jptm.2015.09.17
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- Background
Prenatal tongue development may affect oral-craniofacial structures, but this muscular organ has rarely been investigated. Methods: In order to document the physiology of prenatal tongue growth, we histologically examined the facial and cranial base structures of 56 embryos and 106 fetuses. Results: In Streeter’s stages 13–14 (fertilization age [FA], 28 to 32 days), the tongue protruded into the stomodeal cavity from the retrohyoid space to the cartilaginous mesenchyme of the primitive cranial base, and in Streeter’s stage 15 (FA, 33 to 36 days), the tongue rapidly swelled and compressed the cranial base to initiate spheno-occipital synchondrosis and continued to swell laterally to occupy most of the stomodeal cavity in Streeter’s stage 16–17 (FA, 37 to 43 days). In Streeter’s stage 18–20 (FA, 44 to 51 days), the tongue was vertically positioned and filled the posterior nasopharyngeal space. As the growth of the mandible and maxilla advanced, the tongue was pulled down and protruded anteriorly to form the linguomandibular complex. Angulation between the anterior cranial base (ACB) and the posterior cranial base (PCB) was formed by the emerging tongue at FA 4 weeks and became constant at approximately 124°–126° from FA 6 weeks until birth, which was consistent with angulations measured on adult cephalograms. Conclusions: The early clockwise growth of the ACB to the maxillary plane became harmonious with the counter-clockwise growth of the PCB to the tongue axis during the early prenatal period. These observations suggest that human embryonic tongue growth affects ACB and PCB angulation, stimulates maxillary growth, and induces mandibular movement to achieve the essential functions of oral and maxillofacial structures.
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Natalie Koren, Shir Shust‐Barequet, Tal Weissbach, Oshrat Raviv, Samar Abu Snenh, Efrat Abraham, Tal Cahan, Vered Eisenberg, Vered Yulzari, Efrat Hadi, Laura Adamo, Shali Mazaki Tovi, Reuven Achiron, Zvi Kivilevitch, Boaz Weisz, Eran Kassif Journal of Ultrasound in Medicine.2023; 42(1): 59. CrossRef - Current data on the development of tongue in prenatal period of human ontogenesis
Tatyana A. Alekseeva, Elena D. Lutsay Science and Innovations in Medicine.2022; 7(3): 148. CrossRef - Morphometric development of the tongue in fetal cadavers
Ahmet Dursun, Yadigar Kastamonı, Demet Kacaroglu, Neslihan Yuzbasıoglu, Tolga Ertekın Surgical and Radiologic Anatomy.2020; 42(1): 3. CrossRef - Pigmented Fungiform Papillae of the Tongue and Lingual Fimbriae as Single Presentation in Adult: A Case Report and Literature Review
Meircurius Dwi Condro Surboyo, Diah Savitri Ernawati, Adiastuti Endah Parmadiati, Riyan Iman Marsetyo European Journal of Dentistry.2020; 14(04): 702. CrossRef - Tongue development in stillborns autopsied at different gestational ages
Laura S. Aguiar, Guilherme R. Juliano, Luciano A.M. Silveira, Mariana S. Oliveira, Bianca G.S. Torquato, Gabriela R. Juliano, Márcia F. Araújo, Sanivia Aparecida L. Pereira, Vicente de Paula A. Teixeira, Mara Lúcia F. Ferraz Jornal de Pediatria.2018; 94(6): 616. CrossRef - In Utero Glossoptosis in Fetuses With Robin Sequence
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- Current Concepts and Occurrence of Epithelial Odontogenic Tumors: II. Calcifying Epithelial Odontogenic Tumor Versus Ghost Cell Odontogenic Tumors Derived from Calcifying Odontogenic Cyst
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Suk Keun Lee, Yeon Sook Kim
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Korean J Pathol. 2014;48(3):175-187. Published online June 26, 2014
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DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.3.175
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13,074
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Calcifying epithelial odontogenic tumors (CEOTs) and ghost cell odontogenic tumors (GCOTs) are characteristic odontogenic origin epithelial tumors which produce calcifying materials from transformed epithelial tumor cells. CEOT is a benign odontogenic tumor composed of polygonal epithelial tumor cells that show retrogressive calcific changes, amyloid-like deposition, and clear cytoplasm. Differentially, GCOTs are a group of transient tumors characterized by ghost cell presence, which comprise calcifying cystic odontogenic tumor (CCOT), dentinogenic ghost cell tumor (DGCT), and ghost cell odontogenic carcinoma (GCOC), all derived from calcifying odontogenic cysts (COCs). There is considerable confusion about COCs and GCOTs terminology, but these lesions can be classified as COCs or GCOTs, based on their cystic or tumorous natures, respectively. GCOTs include ameloblastomatous tumors derived from dominant odontogenic cysts classified as CCOTs, ghost cell-rich tumors producing dentinoid materials as DGCTs, and the GCOT malignant counterpart, GCOCs. Many authors have reported CEOTs and GCOTs variably express keratins, β-catenin, BCL-2, BSP, RANKL, OPG, Notch1, Jagged1, TGF-β, SMADs, and other proteins. However, these heterogeneous lesions should be differentially diagnosed to allow for accurate tumor progression and prognosis prediction.
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Takayuki Kurimoto, Tadashi Yamanishi, Takeshi Harada, Keiko Matsuoka, Setsuko Uematsu, Yuri Yamamoto, Yuki Arimura, Takeshi Togawa, Naoko Inoue, Juntaro Nishio Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2019; 31(1): 38. CrossRef - Odontogenic Cysts and Tumors
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- Different Protein Expressions between Peripheral Ameloblastoma and Oral Basal Cell Carcinoma Occurred at the Same Mandibular Molar Area
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Yeon Sook Kim, Suk Keun Lee
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Korean J Pathol. 2014;48(2):151-158. Published online April 28, 2014
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DOI: https://doi.org/10.4132/KoreanJPathol.2014.48.2.151
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Peripheral ameloblastoma (PA) in gingiva is rare and often confused with oral basal cell carcinoma (OBCC). The tissues of one case of PA and one case of OBCC with the same mandibular molar area affected were compared via an immunohistochemical examination using 50 antisera. The PA and OBCC showed similar proliferation of basaloid epithelial strands, but toluidine blue staining revealed that the PA had pinkish juxta-epithelial myxoid tissue, whereas the OBCC was infiltrated by many mast cells. Immunohistochemical comparisons showed that the PA was strongly positive for ameloblastin, KL1, p63, carcinoembryonic antigen, focal adhesion kinase, and cathepsin K, and slightly positive for amelogenin, Krox-25, E-cadherin, and PTCH1, whereas the OBCC was not. On the other hand, the OBCC was strongly positive for EpCam, matrix metalloprotease (MMP)-1, α1-antitrypsin, cytokeratin-7, p53, survivin, pAKT1, transforming growth factor-β1, NRAS, TGase-1, and tumor nescrosis factor-α, and consistently positive for β-catenin, MMP-2, cathepsin G, TGase-2, SOS-1, sonic hedgehog, and the β-defensins-1, -2, -3, while the PA was not. These data suggest that the tumorigeneses of PA and OBCC differ, and that PAs undergo odontogenic differentiation and generate oncogenic signals for infiltrative growth and bone resorption, whereas OBCCs undergo basaloid epidermal differentiation as a result of growth factor/cytokine-related oncogenic signals.
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- Expression of ameloblastin in the human tooth germ and ameloblastoma
Suganya Panneer Selvam, Irulandy Ponniah Oral Diseases.2018; 24(8): 1538. CrossRef - The Use of BEREP4 Immunohistochemistry Staining for Detection of Basal Cell Carcinoma
Anthony Paulo Sunjaya, Angela Felicia Sunjaya, Sukmawati Tansil Tan Journal of Skin Cancer.2017; 2017: 1. CrossRef - Peripheral ameloblastoma of the mandible: A case report
Takahiro Kaneko, Satoshi Nakamura, Ryutarou Kawano, Norio Horie, Tetsuo Shimoyama Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2016; 28(6): 565. CrossRef
- Current Concepts and Occurrence of Epithelial Odontogenic Tumors: I. Ameloblastoma and Adenomatoid Odontogenic Tumor
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Suk Keun Lee, Yeon Sook Kim
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Korean J Pathol. 2013;47(3):191-202. Published online June 25, 2013
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DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.3.191
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Ameloblastomas and adenomatoid odontogenic tumors (AOTs) are common epithelial tumors of odontogenic origin. Ameloblastomas are clinico-pathologically classified into solid/multicystic, unicystic, desmoplastic, and peripheral types, and also divided into follicular, plexiform, acanthomatous, granular types, etc., based on their histological features. Craniopharyngiomas, derived from the remnants of Rathke's pouch or a misplaced enamel organ, are also comparable to the odontogenic tumors. The malignant transformation of ameloblastomas results in the formation of ameloblastic carcinomas and malignant ameloblastomas depending on cytological dysplasia and metastasis, respectively. AOTs are classified into follicular, extrafollicular, and peripheral types. Ameloblastomas are common, have an aggressive behavior and recurrent course, and are rarely metastatic, while AOTs are hamartomatous benign lesions derived from the complex system of the dental lamina or its remnants. With advances in the elucidation of molecular signaling mechanisms in cells, the cytodifferentiation of epithelial tumor cells in ameloblastomas and AOTs can be identified using different biomarkers. Therefore, it is suggested that comprehensive pathological observation including molecular genetic information can provide a more reliable differential diagnosis for the propagation and prognosis of ameloblastomas and AOTs. This study aimed to review the current concepts of ameloblastomas and AOTs and to discuss their clinico-pathological features relevant to tumorigenesis and prognosis.
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