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Journal articles on the topic 'Squamocolumnar junction'

Author: Grafiati

Published: 7 June 2025

Last updated: 16 July 2025

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1

Trudgill, N. J., S. K. Suvarna, K. C. Kapur, and S. A. Riley. "Intestinal metaplasia at the squamocolumnar junction in patients attending for diagnostic gastroscopy." Gut 41, no. 5 (1997): 585–89. http://dx.doi.org/10.1136/gut.41.5.585.

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Background—The incidence of adenocarcinoma of the oesophagus and gastric cardia is increasing rapidly. Barrett’s oesophagus is the major risk factor. Intestinal metaplasia at the squamocolumnar junction in the absence of Barrett’s oesophagus is common but its relation to adenocarcinoma and gastro-oesophageal reflux disease is unclear.Aims—To study the prevalence and clinical, endoscopic, and histological associations of intestinal metaplasia at the squamocolumnar junction.Methods—Biopsy specimens were taken from 120 randomly selected patients undergoing routine diagnostic endoscopy. Eight biop

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2

Park, Young S., Hyo Jin Park, Gyeong Hoon Kang, Chong Jai Kim, and Je G. Chi. "Histology of Gastroesophageal Junction in Fetal and Pediatric Autopsy." Archives of Pathology & Laboratory Medicine 127, no. 4 (2003): 451–55. http://dx.doi.org/10.5858/2003-127-0451-hogjif.

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Abstract Context.—There is much debate over whether the gastric cardia exists from birth as a normal structure or is a metaplastic structure that develops as the result of gastroesophageal reflux disease. This question has become a matter of concern since the incidence of adenocarcinoma at the gastroesophageal junction has been increasing rapidly in the Western world for more than 2 decades. Various groups of investigators have tried to clarify this matter by examining the histology of the gastroesophageal junction in autopsy cases, and there have been striking discrepancies in their findings.

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3

Kahrilas, P. J., S. Lin, J. Chen, and M. Manka. "The effect of hiatus hernia on gastro-oesophageal junction pressure." Gut 44, no. 4 (1999): 476–82. http://dx.doi.org/10.1136/gut.44.4.476.

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BACKGROUNDHiatus hernia and lower oesophageal sphincter hypotension are often viewed as opposing hypotheses for gastro-oesophageal junction incompetence.AIMSTo examine the interaction between hiatus hernia and lower oesophageal sphincter hypotension.METHODSIn seven normal subjects and seven patients with hiatus hernia, the squamocolumnar junction and intragastric margin of the gastro-oesophageal junction were marked with endoscopically placed clips. Axial and radial characteristics of the gastro-oesophageal junction high pressure zone were mapped relative to the hiatus and clips during concurr

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4

Herfs, Michael, and Christopher P. Crum. "Squamocolumnar junction ablation—tying up loose ends?" Nature Reviews Clinical Oncology 12, no. 7 (2015): 378–80. http://dx.doi.org/10.1038/nrclinonc.2015.104.

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5

Zimmer, V., and F. Lammert. "The “swinging” squamocolumnar junction in esophagocardiac achalasia." Endoscopy 44, S 02 (2012): E201. http://dx.doi.org/10.1055/s-0032-1308920.

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6

Reich, Olaf, Sigrid Regauer, W. G. McCluggage, Christine Bergeron, and Charles Redman. "Defining the Cervical Transformation Zone and Squamocolumnar Junction." International Journal of Gynecological Pathology 36, no. 6 (2017): 517–22. http://dx.doi.org/10.1097/pgp.0000000000000381.

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7

Bornstein, J., E. Rueda-Pedraza, D. Winesett, et al. "HISTOLOGIC CHARACTERIZATION OF THE SQUAMOCOLUMNAR JUNCTION IN CHILDREN." Journal of Pediatric Gastroenterology &amp Nutrition 25, no. 4 (1997): 447. http://dx.doi.org/10.1097/00005176-199710000-00036.

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8

Ganesh, Vijaya, Iraj Ghafouri, Joseph J. Apuzzio, Jahir C. Sama, and Leslie Iffy. "Behavior of the squamocolumnar junction during normal pregnancy." American Journal of Obstetrics and Gynecology 154, no. 3 (1986): 689–90. http://dx.doi.org/10.1016/0002-9378(86)90631-9.

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9

Kahrilas, Peter J., Shezhang Lin, Anita E. Spiess, James G. Brasseur, Raymond J. Joehl, and Michael Manka. "Impact of fundoplication on bolus transit across esophagogastric junction." American Journal of Physiology-Gastrointestinal and Liver Physiology 275, no. 6 (1998): G1386—G1393. http://dx.doi.org/10.1152/ajpgi.1998.275.6.g1386.

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This study analyzed the effect of fundoplication on the mechanics of liquid and solid bolus transit across the esophagogastric junction (EGJ). The squamocolumnar junction was endoscopically clipped in seven controls, seven hiatal hernia patients, and seven patients after laparoscopic Nissen fundoplication. Concurrent manometry and fluoroscopy were done during swallows of liquid barium and a 13-mm-diameter marshmallow. The EGJ opening, pressure gradients, transit efficacy, and axial motion were measured. The axial motion of the EGJ was reduced in the fundoplication and hiatal hernia patients. T

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10

Bornstein, J., D. Winesett, E. Rueda-Pedraza, et al. "Histologic characterization of the squamocolumnar junction (SCJ) in children." Gastrointestinal Endoscopy 45, no. 4 (1997): AB59. http://dx.doi.org/10.1016/s0016-5107(97)80139-3.

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11

Bornstein, J., E. Rueda‐Pedraza, D. Winesett, et al. "HISTOLOGIC CHARACTERIZATION OF THE SQUAMOCOLUMNAR JUNCTION IN CHILDREN:19." Journal of Pediatric Gastroenterology and Nutrition 25, no. 4 (1997): 447. http://dx.doi.org/10.1002/j.1536-4801.1997.tb01793.x.

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12

Akter, Latifa, Mehriban Amatullah, Tahsin Tabassum, et al. "Diagnostic Accuracy of Endocervical Curettage in Detecting CIN2+ with Non-Visible Squamocolumnar Junction." Journal of Neonatal Surgery 14, no. 17S (2025): 1030–36. https://doi.org/10.63682/jns.v14i17s.5691.

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Background: Cervical cancer remains a significant health burden, particularly in low-resource settings. Accurate detection of cervical intraepithelial neoplasia grade 2 or worse (CIN2+) is critical for prevention. Colposcopy-directed biopsy (CDB) may miss lesions when the squamocolumnar junction (SCJ) is not visible, especially in women with Type 3 transformation zone (TZ). Endocervical curettage (ECC) has been proposed as a complementary diagnostic tool, though its utility remains underexplored. This study evaluates the diagnostic accuracy of ECC in detecting CIN2+ lesions, particularly in wo

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13

Pascarenco, Ofelia Daniela, Alina Boeriu, Simona Mocan, Ghenadie Pascarenco, Silvia Drasoveanu, and Marinela Galeanu. "Barrett's Esophagus and Intestinal Metaplasia of Gastric Cardia: Prevalence, Clinical, Endoscopic and Histological Features." Journal of Gastrointestinal and Liver Diseases 23, no. 1 (2014): 19–25. http://dx.doi.org/10.15403/jgld-1274.

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Background & Aims: Over the past few decades, the incidence of adenocarcinomas of the gastroesophageal junction has rapidly increased. Barrett's esophagus is a risk factor for esophageal adenocarcinoma, but the role of intestinal metaplasia of the gastric cardia as a precursor in cardia-related cancer is controversial. The aims of the present study were to examine the prevalence of intestinal metaplasia in the gastroesophageal junction and to evaluate the clinical, endoscopical and histological features of patients with intestinal metaplasia in the gastric cardia and patients with Barrett'

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14

Taylor, Jason A., Krishnansu Tewari, Shu Y. Liao, Christopher C. W. Hughes, and Luis P. Villarreal. "Immunohistochemical Analysis, Human Papillomavirus DNA Detection, Hormonal Manipulation, and Exogenous Gene Expression of Normal and Dysplastic Human Cervical Epithelium in Severe Combined Immunodeficiency Mice." Journal of Virology 73, no. 6 (1999): 5144–48. http://dx.doi.org/10.1128/jvi.73.6.5144-5148.1999.

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ABSTRACT The cervical squamocolumnar junction of normal and dysplastic human xenografts was maintained in SCID-beige mice. Dysplastic tissue maintained a dysplastic morphology, irregular pattern of keratin expression, elevated levels of cellular proliferation, and human papillomavirus type 16 and/or type 18 DNA. Hyperplastic changes of normal xenografts occurred via high-dose estrogen exposure, and through recombinant adenovirus infection, the introduction and stable expression of an exogenous gene was accomplished.

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15

RICHTER, J. E. "Intestinal metaplasia and the squamocolumnar junction: what does it all mean?" Gut 42, no. 5 (1998): 604–6. http://dx.doi.org/10.1136/gut.42.5.604.

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16

Hamada, Hiroshige, Ken Haruma, Mitsuhiro Mihara, et al. "4713 Relationship between endoscopic findings of squamocolumnar junction and corpus gastritis." Gastrointestinal Endoscopy 51, no. 4 (2000): AB211. http://dx.doi.org/10.1016/s0016-5107(00)14560-2.

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17

Ferguson, Dawn D., Kenneth R. DeVault, David S. Loeb, and Michael B. Wallace. "Inter-Observer Variability with Enhanced Magnification Endoscopy of the Squamocolumnar Junction." Gastrointestinal Endoscopy 61, no. 5 (2005): AB225. http://dx.doi.org/10.1016/s0016-5107(05)01234-4.

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18

Günther, T., A. Hackelsberger, P. Malfertheiner, and A. Roessner. "Is typing of metaplasia at the squamocolumnar junction revealing its aetiology?" Virchows Archiv 436, no. 1 (2000): 6–11. http://dx.doi.org/10.1007/pl00008200.

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19

Desai, Kanan T., Natasha Hansen, Ana-Cecilia Rodriguez, et al. "Squamocolumnar junction visibility, age, and implications for cervical cancer screening programs." Preventive Medicine 180 (March 2024): 107881. http://dx.doi.org/10.1016/j.ypmed.2024.107881.

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20

Seenan, John P., Angela A. Wirz, Alan T. Clarke, Andrew W. Kelman, and Kenneth E. McColl. "M1833 Strong Correlation Between Squamocolumnar Junction Position and Age in Healthy Volunteers." Gastroenterology 136, no. 5 (2009): A—427. http://dx.doi.org/10.1016/s0016-5085(09)61968-5.

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21

Evans, John A., Brett E. Bouma, Jason Bressner, et al. "Identifying intestinal metaplasia at the squamocolumnar junction by using optical coherence tomography." Gastrointestinal Endoscopy 65, no. 1 (2007): 50–56. http://dx.doi.org/10.1016/j.gie.2006.04.027.

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22

Pandolfino, John E., Qing Zhang, Sudip K. Ghosh, Jennifer Post, Monika Kwiatek, and Peter J. Kahrilas. "Acidity Surrounding the Squamocolumnar Junction in GERD Patients: "Acid Pocket" Versus "Acid Film"." American Journal of Gastroenterology 102, no. 12 (2007): 2633–41. http://dx.doi.org/10.1111/j.1572-0241.2007.01488.x.

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23

Saunders, N., D. Anderson, E. Sheridan, L. Gilbert, and F. Sharp. "Endoscopic localization of the squamocolumnar junction before cervical cone biopsy in 284 patients." Cancer 65, no. 6 (1990): 1312–17. http://dx.doi.org/10.1002/1097-0142(19900315)65:6<1312::aid-cncr2820650610>3.0.co;2-1.

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24

Herfs, Michael, Joan Somja, Brooke E. Howitt, et al. "Unique recurrence patterns of cervical intraepithelial neoplasia after excision of the squamocolumnar junction." International Journal of Cancer 136, no. 5 (2014): 1043–52. http://dx.doi.org/10.1002/ijc.28978.

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25

Clavero, Omar, Jenny McCloskey, Vicente Marco Molina, et al. "Squamous intraepithelial lesions of the anal squamocolumnar junction: Histopathological classification and HPV genotyping." Papillomavirus Research 3 (June 2017): 11–17. http://dx.doi.org/10.1016/j.pvr.2016.12.001.

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26

Jin, Ramon, Sarah To, Yuanwei Xu, et al. "278: SOX2 LOSS RESULTS IN EXPANSION OF METAPLASTIC GLANDS AT THE SQUAMOCOLUMNAR JUNCTION." Gastroenterology 169, no. 1 (2025): S—76. https://doi.org/10.1016/s0016-5085(25)01124-2.

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27

Huang, Qin. "Definition of the Esophagogastric Junction: A Critical Mini Review." Archives of Pathology & Laboratory Medicine 135, no. 3 (2011): 384–89. http://dx.doi.org/10.5858/2010-0162-ra.1.

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Abstract Context.—Accurate diagnosis of diseases involving the esophagogastric junction (EGJ) is challenging because of difficulty in defining the EGJ endoscopically and histologically. Recent research results have redefined the EGJ, and the endoscopic and histologic diagnostic criteria of the mucosal EGJ have become available. Objective.—To review the recent literature on endoscopy, histology, and pathology of the EGJ with critical analysis. Data Sources.—Recently published research articles and guidelines in the peer-reviewed core journals and personal research results in this field. Conclus

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28

Lee, Thomas J., John E. Pandolfino, Kelly Goelz, Bryan Trueworthy, and Peter J. Kahrilas. "Esophageal acid exposure at 1 cm and 6 cm above the squamocolumnar junction (SCJ)." Gastroenterology 124, no. 4 (2003): A72. http://dx.doi.org/10.1016/s0016-5085(03)80356-6.

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29

Bartel, Michael J., Nora R. Ratcliffe, Scott A. Hirschman, et al. "Su1468 Subsquamous Intestinal Metaplasia Is Common At the Squamocolumnar Junction in Native Barrett's Esophagus." Gastrointestinal Endoscopy 73, no. 4 (2011): AB274. http://dx.doi.org/10.1016/j.gie.2011.03.521.

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30

Herfs, M., Y. Yamamoto, A. Laury, et al. "A discrete population of squamocolumnar junction cells implicated in the pathogenesis of cervical cancer." Proceedings of the National Academy of Sciences 109, no. 26 (2012): 10516–21. http://dx.doi.org/10.1073/pnas.1202684109.

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31

Schneider, Philip, Steven Hinrichs, Rebecca Zulim, Reid Towery, Chantey Morris, and Sidney S. Mirvish. "Carcinogenesis by methylbenzylnitrosamine near the squamocolumnar junction and methylamylnitrosamine metabolism in the mouse forestomach." Cancer Letters 102, no. 1-2 (1996): 125–31. http://dx.doi.org/10.1016/0304-3835(96)04155-9.

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32

Maru, Yoshiaki, Akira Kawata, Ayumi Taguchi, et al. "Establishment and Molecular Phenotyping of Organoids from the Squamocolumnar Junction Region of the Uterine Cervix." Cancers 12, no. 3 (2020): 694. http://dx.doi.org/10.3390/cancers12030694.

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The metaplastic epithelium of the transformation zone (TZ) including the squamocolumnar junction (SCJ) of the uterine cervix is a prime target of human papilloma virus (HPV) infection and subsequent cancer development. Due to the lack of adequate in vitro models for SCJ, however, investigations into its physiological roles and vulnerability to carcinogenesis have been limited. By using Matrigel-based three-dimensional culture techniques, we propagated organoids derived from the normal SCJ region, along with metaplastic squamous cells in the TZ. Consisting predominantly of squamous cells, organ

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33

Thompson, Cayla, Bridget Kohlnhofer, Roman Stavniichuk, et al. "GATA4 Regulates Development of the Squamocolumnar Junction in the GI Tract: Implications for Barrett's Esophagus." Gastroenterology 152, no. 5 (2017): S87. http://dx.doi.org/10.1016/s0016-5085(17)30639-x.

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34

Phillips, Hannah, Jeffrey Fetzer, John League, Nayantara Coelho-Prabhu, and Cadman L. Leggett. "Sa2020 APPLICATION OF THE MINKOWSKI-BOULIGAND DIMENSION TO STANDARDIZE THE DEFINITION OF THE SQUAMOCOLUMNAR JUNCTION." Gastroenterology 166, no. 5 (2024): S—606. http://dx.doi.org/10.1016/s0016-5085(24)01856-0.

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35

Vins, Neethu, Subi Sugathan, Asma Al Menhali, and Sherif M. Karam. "Overgrowth of Squamocolumnar Junction and Dysregulation of Stem Cell Lineages in the Stomach of Vitamin A-Deficient Mice." Nutrients 14, no. 16 (2022): 3334. http://dx.doi.org/10.3390/nu14163334.

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Junctional epithelia are common sites for pathological transformations. In mice, the stratified epithelium of the forestomach joins the simple glandular epithelium of the cardia at the limiting ridge. We previously demonstrated the expression of vitamin A receptors in the gastric stem/progenitor cells and their progeny and found that excess retinoic acid enhances cellular dynamics of gastric epithelium. This study examines how deficiency of vitamin A would alter gastric epithelial stem cell lineages. Three-week-old mice of both genders were weaned and fed with a vitamin A deficient (VAD) diet

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36

Sun, Jing, Elena V. Komissarova, Caitlin Hills, et al. "Abstract 929: CDKN2A/p16 knockout in LGR5+ progenitor cells augments mucous gland hyperplasia/metaplasia, inflammation, and dysplasia in mouse stomach squamocolumnar junction." Cancer Research 82, no. 12_Supplement (2022): 929. http://dx.doi.org/10.1158/1538-7445.am2022-929.

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Abstract Background: Esophageal adenocarcinoma (EAC) develops in pre-cancer columno-glandular hyperplasia, intestinal metaplasia and dysplasia that replaces squamous epithelium and characterizes Barrett’s esophagus (BE). We reported CDKN2A/p16 deletions in up to 69% of BE patients who progressed to dysplasia and EAC, suggesting that p16 loss may drive progression of BE to EAC. LGR5+ cardia like stem cells in the squamocolumnar junction (SCJ) of mouse stomach have been implicated in the cellular origins of BE, and glandular hyperplasia/metaplasia (MGHP) and dysplasia and enhanced inflammation i

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37

Guerrero Garcia Hall, Mats, Jörgen Wenner, and Stefan Öberg. "The normal squamocolumnar junction is circumferentially even and minimal irregularities are manifestations of gastroesophageal acid reflux." Scandinavian Journal of Gastroenterology 52, no. 3 (2016): 270–75. http://dx.doi.org/10.1080/00365521.2016.1249402.

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38

Wallner, Bengt, Anders Sylvan, and Karl-Gunnar Janunger. "Endoscopic assessment of the “Z-line” (squamocolumnar junction) appearance: Reproducibility of the ZAP classification among endoscopists." Gastrointestinal Endoscopy 55, no. 1 (2002): 65–69. http://dx.doi.org/10.1067/mge.2002.119876.

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39

Wenner, Jörgen, Mats Hall, Peter Höglund, Jan Johansson, Folke Johnsson, and Stefan Öberg. "Wireless pH Recording Immediately Above the Squamocolumnar Junction Improves the Diagnostic Performance of Esophageal pH Studies." American Journal of Gastroenterology 103, no. 12 (2008): 2977–85. http://dx.doi.org/10.1111/j.1572-0241.2008.02174.x.

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40

Herfs, Michael, Carlos Parra-Herran, Brooke E. Howitt, et al. "Cervical Squamocolumnar Junction–specific Markers Define Distinct, Clinically Relevant Subsets of Low-grade Squamous Intraepithelial Lesions." American Journal of Surgical Pathology 37, no. 9 (2013): 1311–18. http://dx.doi.org/10.1097/pas.0b013e3182989ee2.

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41

Fletcher, J. "Studies of acid exposure immediately above the gastro-oesophageal squamocolumnar junction: evidence of short segment reflux." Gut 53, no. 2 (2004): 168–73. http://dx.doi.org/10.1136/gut.2003.022160.

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42

Pace, F., S. Pallotta, D. Foschi, G. Bianchi Porro, and E. Trabucchi. "Absence of distinctive cells in the squamocolumnar junction of patients with Barrett's esophagus: An ultramicroscopic study." Digestive and Liver Disease 32 (November 2000): A59. http://dx.doi.org/10.1016/s1590-8658(00)80414-4.

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43

Akiyama, Jun-ichi, Kei Matsueda, Shoda Ryosuke, et al. "Pathophysiological features of decreased vascularity around squamocolumnar junction in patients with endoscopy-negative gastroesophageal reflux disease." Gastroenterology 118, no. 4 (2000): A477. http://dx.doi.org/10.1016/s0016-5085(00)84023-8.

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44

Sawhney, Roger A., Helen M. Shields, Carol H. Allan, Jason A. Boch, Jerry S. Trier, and Donald A. Antonioli. "Morphological characterization of the squamocolumnar junction of the esophagus in patients with and without Barrett's epithelium." Digestive Diseases and Sciences 41, no. 6 (1996): 1088–98. http://dx.doi.org/10.1007/bf02088224.

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45

Olson, D. R. "Cervical Squamocolumnar Junction–specific Markers Define Distinct, Clinically Relevant Subsets of Low-grade Squamous Intraepithelial Lesions." Yearbook of Pathology and Laboratory Medicine 2014 (2014): 92–95. https://doi.org/10.1016/j.ypat.2014.02.001.

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46

Phillips, Hannah, Jeffrey Fetzer, Amr Ali, et al. "Sa2070: COMPUTER-ASSISTED CORRELATION OF SHAPE COMPLEXITY OF THE SQUAMOCOLUMNAR JUNCTION TO PRESENCE OF INTESTINAL METAPLASIA." Gastroenterology 169, no. 1 (2025): S—640. https://doi.org/10.1016/s0016-5085(25)02409-6.

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47

Timaran, Carlos H., Yash P. Sangwan, and Julio A. Solla. "Adenocarcinoma in a Hemorrhoidectomy Specimen: Case Report and Review of the Literature." American Surgeon 66, no. 8 (2000): 789–92. http://dx.doi.org/10.1177/000313480006600821.

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Our purpose is to report a case of unexpected anal adenocarcinoma found in a hemorrhoidectomy specimen. A review of the literature, with emphasis on extramucosal anal adenocarcinoma as a pathologic entity, is included. Our patient presented with a 2-year history of grade III prolapsing internal hemorrhoids. A hemorrhoidectomy was performed and gross examination of the specimen was unremarkable. The pathologic evaluation revealed microinvasive well-differentiated adenocarcinoma at the squamocolumnar junction. There was neither an apparent connection with the overlying mucosa nor an in situ comp

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48

VARDAR, Rukiye, Enver VARDAR, and Serhat BOR. "Is the prevalence of intestinal metaplasia at the squamocolumnar junction different in patients with progressive sytemic sclerosis?" Turkish Journal of Gastroenterology 21, no. 3 (2010): 251–56. http://dx.doi.org/10.4318/tjg.2010.0096.

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49

Oksanen, A. "Inflammation and intestinal metaplasia at the squamocolumnar junction in young patients with or without Helicobacter pylori infection." Gut 52, no. 2 (2003): 194–98. http://dx.doi.org/10.1136/gut.52.2.194.

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50

Pace, Fabio, S. Pallotta, D. Foschi, G. Bianchi Porro, and E. Trabucchi. "Absence of distinctive cells in the squamocolumnar junction of patients with Barrett's esophagus (BE): An ultramicroscopic study." Gastroenterology 118, no. 4 (2000): A227. http://dx.doi.org/10.1016/s0016-5085(00)82983-2.

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