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Journal articles on the topic 'Calcifying Tumor Markers'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Shah, Yashvi, Rashmi Metgud, Smitha Naik, and Aniruddh Tak. "Immunohistochemistry in Oral Pathologies: Diagnostic and Prognostic Perspectives." IOSR Journal of Dental and Medical Sciences 24, no. 6 (2025): 40–46. https://doi.org/10.9790/0853-2406054046.

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Immunohistochemistry (IHC) has revolutionized the diagnostic and prognostic landscape of oral pathology by enabling precise detection of specific antigens within tissue sections. This article offers a comprehensive overview of IHC’s evolution, fundamental principles, and practical techniques—ranging from direct and indirect labeling to advanced polymer- and gold-based methods. Emphasis is placed on the meticulous preparation of tissues, including formalin fixation and antigen retrieval, to ensure reliable staining outcomes. A detailed exploration of molecular markers follows, illustrating how

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2

Crocker, Melissa K., Evgenia Gourgari, Maya Lodish, and Constantine A. Stratakis. "Use of Aromatase Inhibitors in Large Cell Calcifying Sertoli Cell Tumors: Effects on Gynecomastia, Growth Velocity, and Bone Age." Journal of Clinical Endocrinology & Metabolism 99, no. 12 (2014): E2673—E2680. http://dx.doi.org/10.1210/jc.2014-2530.

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Context: Large cell calcifying Sertoli cell tumors (LCCSCT) present in isolation or, especially in children, in association with Carney Complex (CNC) or Peutz-Jeghers Syndrome (PJS). These tumors overexpress aromatase (CYP19A1), which leads to increased conversion of delta-4-androstenedione to estrone and testosterone to estradiol. Prepubertal boys may present with growth acceleration, advanced bone age, and gynecomastia. Objective: To investigate the outcomes of aromatase inhibitor therapy (AIT) in prepubertal boys with LCCSCTs. Design: Case series of a very rare tumor and chart review of cas

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3

Zhou, Jun, Luting Zhou, Sheng Wu, et al. "Clinicopathologic Study of Calcifying Fibrous Tumor Emphasizing Different Anatomical Distribution and Favorable Prognosis." BioMed Research International 2019 (July 2, 2019): 1–8. http://dx.doi.org/10.1155/2019/5026860.

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Aims. Calcifying fibrous tumor (CFT) is a very rare begin fibroblastic tumor featuring a widely anatomical distribution and may mimic various spindle cell tumors. Misdiagnosis and hence mistreatment are likely caused due to unfamiliarity to clinicians or junior pathologists. We collected a relatively large series of CFTs in our institution aiming at further summarizing their clinicopathologic features in Chinese patients and discussing the diagnosis and differential diagnosis in clinical practice. Methods. Clinicopathologic data of 22 CFTs were retrospectively reviewed. Histologic features wer

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4

Kulkarni, Spoorti, Harishanker Alampally, Vasudev Guddattu, Gabriel Rodrigues, and Sunitha Carnelio. "Expression of Fascin and SALL4 in odontogenic cysts and tumors: an immunohistochemical appraisal." F1000Research 11 (June 27, 2024): 1578. http://dx.doi.org/10.12688/f1000research.126091.5.

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Background Various stemness markers (SOX2, OCT4, and NANOG) have been studied in odontogenic cysts and tumors. However, studies on SALL4 having similar properties of stemness has not been documented. Additionally, insight into fascin as a migratory molecule is less explored. In this study, the expression of SALL4 and fascin were evaluated in ameloblastoma, adenomatoid odontogenic tumor (AOT), odontogenic keratocyst (OKC), dentigerous cyst (DC), radicular cyst (RC), and calcifying odontogenic cyst (COC). Methods Semi-quantitative analysis of fascin and SALL4 immuno-positive cells was done in a

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Kulkarni, Spoorti, Harishanker Alampally, Vasudev Guddattu, Gabriel Rodrigues, and Sunitha Carnelio. "Expression of Fascin and SALL4 in odontogenic cysts and tumors: an immunohistochemical appraisal." F1000Research 11 (December 23, 2022): 1578. http://dx.doi.org/10.12688/f1000research.126091.1.

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Background: Various stemness markers (SOX2, OCT4, and NANOG) have been studied in odontogenic cysts and tumors. However, studies on SALL4 having similar properties of stemness has not been documented. Additionally, insight into fascin as a migratory molecule is less explored. In this study, the expression of SALL4 and fascin were evaluated in ameloblastoma, adenomatoid odontogenic tumor (AOT), odontogenic keratocyst (OKC), dentigerous cyst (DC), radicular cyst (RC), and calcifying odontogenic cyst (COC). Methods: Semi-quantitative analysis of fascin and SALL4 immuno-positive cells was done in

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Kulkarni, Spoorti, Harishanker Alampally, Vasudev Guddattu, Gabriel Rodrigues, and Sunitha Carnelio. "Expression of Fascin and SALL4 in odontogenic cysts and tumors: an immunohistochemical appraisal." F1000Research 11 (December 14, 2023): 1578. http://dx.doi.org/10.12688/f1000research.126091.3.

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Background Various stemness markers (SOX2, OCT4, and NANOG) have been studied in odontogenic cysts and tumors. However, studies on SALL4 having similar properties of stemness has not been documented. Additionally, insight into fascin as a migratory molecule is less explored. In this study, the expression of SALL4 and fascin were evaluated in ameloblastoma, adenomatoid odontogenic tumor (AOT), odontogenic keratocyst (OKC), dentigerous cyst (DC), radicular cyst (RC), and calcifying odontogenic cyst (COC). Methods Semi-quantitative analysis of fascin and SALL4 immuno-positive cells was done in a

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7

Kulkarni, Spoorti, Harishanker Alampally, Vasudev Guddattu, Gabriel Rodrigues, and Sunitha Carnelio. "Expression of Fascin and SALL4 in odontogenic cysts and tumors: an immunohistochemical appraisal." F1000Research 11 (June 10, 2024): 1578. http://dx.doi.org/10.12688/f1000research.126091.4.

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Background Various stemness markers (SOX2, OCT4, and NANOG) have been studied in odontogenic cysts and tumors. However, studies on SALL4 having similar properties of stemness has not been documented. Additionally, insight into fascin as a migratory molecule is less explored. In this study, the expression of SALL4 and fascin were evaluated in ameloblastoma, adenomatoid odontogenic tumor (AOT), odontogenic keratocyst (OKC), dentigerous cyst (DC), radicular cyst (RC), and calcifying odontogenic cyst (COC). Methods Semi-quantitative analysis of fascin and SALL4 immuno-positive cells was done in a

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8

Kulkarni, Spoorti, Harishanker Alampally, Vasudev Guddattu, Gabriel Rodrigues, and Sunitha Carnelio. "Expression of Fascin and SALL4 in odontogenic cysts and tumors: an immunohistochemical appraisal." F1000Research 11 (September 1, 2023): 1578. http://dx.doi.org/10.12688/f1000research.126091.2.

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Background: Various stemness markers (SOX2, OCT4, and NANOG) have been studied in odontogenic cysts and tumors. However, studies on SALL4 having similar properties of stemness has not been documented. Additionally, insight into fascin as a migratory molecule is less explored. Following a thorough literature search we hypothesize that fascin might contribute for the local migratory behaviour of the odontogenic epithelial cells in tumors and cysts while SALL4 may contribute to stemness property. Thus, the aim of the present study was to evaluate the expression of fascin and SALL4 in histopatholo

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9

Lefevre, Hervé, Claire Bouvattier, Najiba Lahlou, Catherine Adamsbaum, Pierre Bougnères, and Jean-Claude Carel. "Prepubertal gynecomastia in Peutz-Jeghers syndrome: incomplete penetrance in a familial case and management with an aromatase inhibitor." European Journal of Endocrinology 154, no. 2 (2006): 221–27. http://dx.doi.org/10.1530/eje.1.02085.

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Background: Peutz-Jeghers syndrome (PJS) is a rare autosomal-dominant disorder characterized by multiple gastrointestinal hamartomatous polyps, mucocutaneous pigmentation and increased predisposition to various neoplasms. Endocrine manifestations in PJS include gynecomastia due to calcified Sertoli cell testicular tumors usually referred to as large-cell calcifying Sertoli cell tumors (LSCT). Objective: To evaluate the value of endocrine markers and aromatase inhibitor treatment in children with PJS and LSCT. Design and setting: Familial cases, followed in a tertiary care center. Patients: Two

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10

Simões-Pereira, Joana, Filipa Santos, Lurdes Lopes, and Catarina Limbert. "Prepubertal gynaecomastia in a boy with Peutz-Jeghers syndrome: managing the aromatase overexpression." Journal of Pediatric Endocrinology and Metabolism 31, no. 10 (2018): 1149–54. http://dx.doi.org/10.1515/jpem-2017-0455.

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Abstract Background Gynaecomastia, although rarely related to testicular tumours, in boys with Peutz-Jeghers syndrome (PJS) usually occurs due to large-cell calcifying Sertoli cell tumour (LCCSCT). Case presentation A 4-year-old boy, with a genetic diagnosis of PJS, presented gynaecomastia since the age of 2, associated with increased height velocity (HV). He exhibited bilateral breast enlargement (Tanner-B4) and a testicular volume of 4 mL. Testicular ultrasound revealed multifocal microcalcifications in both testicles. A laboratory evaluation showed undetectable gonadotrophins, testosterone

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11

Takabatake, Kazuya, Tomohiro Arita, Yoshiaki Kuriu, et al. "Calcifying fibrous tumor of the ileum resected by single-port laparoscopic surgery: a case report." Surgical Case Reports 8, no. 1 (2022). http://dx.doi.org/10.1186/s40792-022-01423-8.

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Abstract Background Calcifying fibrous tumors (CFTs) are rare benign tumors. Because CFTs sometimes relapse, radical resection with adequate margins is necessary. We report a case of ileal CFT resected using single-port laparoscopic surgery. Case presentation A 33-year-old man presented with chief complaints of abdominal pain and vomiting. Computed tomography demonstrated a 45-mm-sized pelvic mass with partial calcification in the ileum. The patient was diagnosed with an ileal tumor, and partial resection of the ileum was performed using the single-port laparoscopic technique. Pathologic findi

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12

Yang, Kaiyun, Kesava Reddy, Bill H. Wang, et al. "Immunohistochemical Markers in the Diagnosis of Calcifying Pseudoneoplasm of the Neuraxis." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, August 17, 2020, 1–8. http://dx.doi.org/10.1017/cjn.2020.175.

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ABSTRACT: Background: Calcifying pseudoneoplasm of the neuraxis (CAPNON) is a rare tumor-like lesion with unknown pathogenesis. It is likely under-reported due to diagnostic challenges including the nonspecific radiographic features, lack of diagnostic markers, and often asymptomatic nature of the lesions. Methods: We performed detailed examination of 11 CAPNON specimens diagnosed by histopathology, with the help of electron microscopy and immunohistochemistry. Results: Electron microscopy revealed the presence of fibrillary materials consistent with neurofilaments. In addition to some entrapp

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13

Jayasheelan, Shikha, Saraswathy Sreeram, Akash NS, and Abhay Mohan. "GIST-ery solved: story of an intestinal mass in a young lady." Journal of Surgical Case Reports 2024, no. 11 (2024). http://dx.doi.org/10.1093/jscr/rjae687.

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Abstract A 19-year-old woman presented with abdominal pain and a palpable mass, initially suspected to be a gastrointestinal stromal tumor (GIST) based on imaging. Surgical excision revealed a sclerotic spindle cell neoplasm with minimal cytological atypia, but immunohistochemistry (IHC) was negative for GIST-specific markers. The pan-negative IHC profile, along with calcification foci and low Ki67 index (&lt;1%), led to a diagnosis of calcifying fibrous tumor (CFT). This case highlights the importance of precise diagnostic evaluation and consideration of rare entities like CFT. Comprehens

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14

Jover, E., L. Matilla, M. Garaikoetxea, et al. "Regulation of neutrophil gelatinase-associated lipocalin in aortic valve stenosis." European Heart Journal 42, Supplement_1 (2021). http://dx.doi.org/10.1093/eurheartj/ehab724.1557.

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Abstract Background Aortic valve (AV) stenosis is the commonest form of adult valvular heart disease (VHD) and affects 4.5% of the general population aged over 60 years. Owing to multifactorial and complex molecular events, the valve interstitial cell (VIC) undergoes myofibroblast and osteoblast differentiation. Neutrophil gelatinase-associated lipocalin (NGAL) is a pleiotropic glycoprotein belonging to the lipocalin family and it is expressed in a wide range of tissues and cell types. It is deregulated in several diseases with both detrimental and beneficial effects. NGAL mainly signals towar

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15

Phattarataratip, Ekarat, Tarit Panitkul, Watunyoo Khodkaew, Pattarapong Anupuntanun, Jirapat Jaroonvechatam, and Sirawit Pitarangsikul. "Expression of SOX2 and OCT4 in odontogenic cysts and tumors." Head & Face Medicine 17, no. 1 (2021). http://dx.doi.org/10.1186/s13005-021-00283-1.

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Abstract Background Aberrant expression of stem cell markers has been observed in several types of neoplasms. This trait attributes to the acquired stem-like property of tumor cells and can impact patient prognosis. The objective of this study was to comparatively analyze the expression and significance of SOX2 and OCT4 in various types of odontogenic cysts and tumors. Methods Fifty-five cases of odontogenic cysts and tumors, including 15 ameloblastomas (AM), 5 adenomatoid odontogenic tumors (AOT), 5 ameloblastic fibromas (AF), 5 calcifying odontogenic cysts (COC), 10 dentigerous cysts (DC) an

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16

Ng, K. H., and C. H. Siar. "A clinicopathological and immunohistochemical study of the calcifying epithelial odontogenic tumour (Pindborg tumour) in Malaysians." June 19, 2017. https://doi.org/10.5281/zenodo.811972.

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We reviewed the clinicopathological characteristics of 13 cases of calcifying epithelial odontogenic tumour (CEOT) (Pindborg tumour) diagnosed in the Division on Stomatology, Institute for Medical Research, Kuala Lumpur, over a 29-year period. There were eight female and five male patients. These consisted of eight (61.5 per cent) Malays, three (23.1 per cent) Chinese, one (7.7 per cent) Indian and one (7.7 per cent) Melanau. Their ages at presentation ranged from 19-61 years (mean age, 31.8 years). There were 12 central and one peripheral CEOT. Of these, 76.9 per cent of cases were located in

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Oh, Kyu-Young, Ji-Hoon Kim та Hye-Jung Yoon. "Diagnostic Utility of SATB2, CDX2, CD10, and β-Catenin Immunohistochemistry in WNT Pathway–Altered Odontogenic Tumors". Archives of Pathology & Laboratory Medicine, 9 квітня 2025. https://doi.org/10.5858/arpa.2024-0416-oa.

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Context.— Although WNT pathway–altered odontogenic tumors (WNT-OTs) are a genetically distinct group of odontogenic tumors (OTs), they may histologically resemble other OTs. Objective.— To investigate the utility of immunohistochemical markers in the diagnosis of WNT-OTs. Design.— Immunohistochemistry for SATB2 (SATB homeobox 2), CDX2 (caudal type homeobox 2), CD10, and β-catenin was performed in 37 OTs consisting of 19 WNT-OTs (10 calcifying odontogenic cysts, 7 dentinogenic ghost cell tumors [DGCTs]/adenoid ameloblastomas [AAs], 2 ghost cell odontogenic carcinomas) and 18 non–WNT-OTs (7 unic

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Tahasildar, Jyoti, Sharada Prakash, Vinod Kumar K, et al. "Comparison of b-Catenin Protein Expression in Calcifying Odontogenic Cyst and Dentinogenic Ghost Cell Tumour." JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2022. http://dx.doi.org/10.7860/jcdr/2022/57001.16891.

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Introduction: Calcifying Cystic Odontogenic Tumour (CCOT)/ Calcifying Odontogenic Cyst (COC) display a varying tissue morphology, while exhibiting different biological progression also at the same time. Attempts at classifying COC have largely been unsuccessful due to the present lack of knowledge about the development of these tumours and their underlying molecular changes. Wingless-beta catenin (Wnt–β catenin) signalling pathway has been found to be a cornerstone in the ectodermal development and tumour initiation-progression to malignant tumours, but its specific role in the pathogenesis of

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