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Journal articles on the topic 'Oropharyngeal mass'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Fleisher, Kenneth E., Eric R. Carlson, and S. J. Schaberg. "Oropharyngeal mass." Journal of Oral and Maxillofacial Surgery 56, no. 3 (1998): 359–64. http://dx.doi.org/10.1016/s0278-2391(98)90116-1.

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2

Kalra, R., P. C. Sagar, R. C. Kapoor, and T. K. Prasad. "Chordoma presenting as oropharyngeal mass." Indian Journal of Otolaryngology 41, no. 4 (1989): 166–67. http://dx.doi.org/10.1007/bf02993835.

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3

Pang, Yennie L. I., Alice K. Y. Siu, and Pak C. Ng. "Encephalocele presenting as an oropharyngeal mass." Archives of Disease in Childhood - Fetal and Neonatal Edition 100, no. 3 (2014): F275. http://dx.doi.org/10.1136/archdischild-2014-307689.

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4

Dorjee, Lham. "Rhinosporidiosis presenting as an Oropharyngeal Mass." SBV Journal of Basic, Clinical and Applied Health Science 1, A4 (2018): 148–49. http://dx.doi.org/10.5005/jp-journals-10082-01141.

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5

Kim, Jeong Hong, and Ju Wan Kang. "Oropharyngeal Mass Causing Obstructive Sleep Apnea." JAMA Otolaryngology–Head & Neck Surgery 141, no. 4 (2015): 393. http://dx.doi.org/10.1001/jamaoto.2014.3729.

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6

Choudhury, Tauhidul Alam, Ronica Baruah, Naushad Shah, Brajendra Lahkar, Kuddush Ahmed, and Bhaskar Jyoti Sarmah. "Disseminated Histoplasmosis presenting as oropharyngeal mass lesion." Medical Mycology Case Reports 24 (June 2019): 78–81. http://dx.doi.org/10.1016/j.mmcr.2019.04.013.

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7

Taylan, Gun. "Giant antrochoanal polyp presenting as oropharyngeal mass." Archives of Otolaryngology and Rhinology 3, no. 3 (2017): 103–5. https://doi.org/10.17352/2455-1759.000058.

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Antrochoanal polyps are benign mucosal lesions emerging from the maxillary sinus. The primary symptoms are nasal obstruction and rhinorrhea. Endoscopic and radiological appearance of the disease is typical. These polyps are usually presented unilaterally, although bilateral presentation is also possible. In this paper, we report a case of atypically giant antrochoanal polyp in a 13-year-old child. The patient’s primary complaint was a sensation of lump in her throat. The examination revealed a mass behind soft palate. The excised polyp had the histological characteristic of an angiomatou

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8

Stadlhofer, Rupert, Manuela Moritz, Marceline M. Fuh, et al. "Lipidome Analysis of Oropharyngeal Tumor Tissues Using Nanosecond Infrared Laser (NIRL) Tissue Sampling and Subsequent Mass Spectrometry." International Journal of Molecular Sciences 24, no. 9 (2023): 7820. http://dx.doi.org/10.3390/ijms24097820.

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Ultrashort pulse infrared lasers can simultaneously sample and homogenize biological tissue using desorption by impulsive vibrational excitation (DIVE). With growing attention on alterations in lipid metabolism in malignant disease, mass spectrometry (MS)-based lipidomic analysis has become an emerging topic in cancer research. In this pilot study, we investigated the feasibility of tissue sampling with a nanosecond infrared laser (NIRL) for the subsequent lipidomic analysis of oropharyngeal tissues, and its potential to discriminate oropharyngeal squamous cell carcinoma (OPSCC) from non-tumor

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9

Little, M., and S. Akhtar. "Oropharyngeal mass diagnosed as a large cervical osteophyte." British Journal of Oral and Maxillofacial Surgery 47, no. 1 (2009): 82–83. http://dx.doi.org/10.1016/j.bjoms.2008.06.005.

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10

Balasubramanian, Anusha, Rohaizam Jaafar, Ramiza Ramza Ramli, and Norhafiza Mat Lazim. "Large Vallecula Lipoma: An unusual clinical entity." Bangladesh Journal of Medical Science 15, no. 4 (2016): 621–23. http://dx.doi.org/10.3329/bjms.v15i4.23194.

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Lipoma of the oropharynx is an extremely rare entity with less than ten cases reported in so far. We present the case of a 55-year-old gentleman who was referred to our team for an incidental finding of an oropharyngeal mass. Although he did not have stridor despite the mass occupying almost 80% of his oropharynx, he did complain of progressive voice change, feeling of something in the throat and dysphagia over a period of 2 years. The mass was successfully excised endoscopically without the need for a tracheostomy. Airway issues, management options of an oropharyngeal mass, as well as the app

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11

Corbett, J., D. Wilke, J. Trites, and N. Lamond. "Orbital mass as first presentation of metastatic p16-positive oropharyngeal squamous cell carcinoma." Current Oncology 24, no. 6 (2017): 551. http://dx.doi.org/10.3747/co.24.3523.

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We describe a case in which a 67-year-old man was diagnosed with a metastatic recurrence of p16-positive oropharyngeal squamous cell carcinoma after presenting with a medial orbital mass in the region of the nasolacrimal apparatus. A review of the literature revealed that metastasis to the orbit from any malignancy is an uncommon occurrence, and no cases of p16-positive oropharyngeal squamous cell carcinoma have previously been reported. Our case highlights the importance of maintaining a high index of suspicion during surveillance visits with such patients.

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12

Singh, Kanwar Vikrant, Gurpreet Singh, Surabhi Gupta, and Paromita Patra. "Non-syndromic oropharyngeal hamartoma: A case report." Romanian Medical Journal 71, no. 1 (2024): 49–54. http://dx.doi.org/10.37897/rmj.2024.1.9.

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This case report details the presentation, investigation, management, and histopathological examination of a rare occurrence – non-syndromic oropharyngeal hamartomas in a 2-year-old child. The child presented with a substantial orofacial mass on the dorsum of the tongue, causing significant functional impairments. Notably, the mass measured 8×4 cm and protruded outside the oral cavity. Additional findings included a nodular mass at the tongue tip, a lobulated mass on the right buccal mucosa (3×4 cm), cleft palate, microphthalmos of the right eye, and an accessory pinna on the right cheek. Diag

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13

Kanwar, Vikrant Singh, Singh Gurpreet, Gupta Surabhi, and Patra Paromita. "Non-Syndromic Oropharyngeal Hamartoma: A Case Report." International Journal of Pharmaceutical and Clinical Research 16, no. 1 (2024): 834–40. https://doi.org/10.5281/zenodo.11100613.

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This case report details the presentation, investigation, management, and histopathological examination of a rare occurrence – non-syndromic oropharyngeal hamartomas in a 2-year-old child. The child presented with a substantial orofacial mass on the dorsum of the tongue, causing significant functional impairments. Notably, the mass measured 8×4 cm and protruded outside the oral cavity. Additional findings included a nodular mass at the tongue tip, a lobulated mass on the right buccal mucosa (3×4 cm), cleft palate, microphthalmus of the right eye, and an accessory pinna on the

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14

Rameh, Charbel, Arnaud Deveze, Jean-Pierre Lavieille, Jacques Magnan, and Melanie Sanjuan. "Accidental Removal of a Carotid Endovascular Stent during Oropharyngeal Mass Biopsy." International Journal of Otolaryngology 2009 (2009): 1–3. http://dx.doi.org/10.1155/2009/378683.

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A 54-year-old male patient, with a history of a right mandibular adenocarcinoma, previously excised, and treated with post operative chemo- and radio-therapy, presented with a right oropharyngeal necrotic mass of several months duration. His history is pertinent for a right internal carotid endovascular stenting 2 years prior to presentation. During biopsy of his oropharyngeal lesion, a specimen of tissue was retrieved, with the carotid stent within. There was no bleeding. To the best of our knowledge, there is no such case reported in the literature. We present this case as a reminder on the

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15

Wannemuehler, Todd J., Christopher R. Deig, Brandon P. Brown, and Stuart A. Morgenstein. "Obstructing in Utero Oropharyngeal Mass: Case Report of a Lymphatic Malformation Arising within an Oropharyngeal Teratoma." Ear, Nose & Throat Journal 96, no. 1 (2017): E37—E40. http://dx.doi.org/10.1177/014556131709600106.

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An ex utero intrapartum treatment procedure was performed to deliver a fetus with a multiseptated, entirely cystic, 4.5 × 5.0 × 4.0-cm mass occupying the oropharynx and oral cavity with protrusion from the mouth. Surgical excision was performed, and final pathologic diagnosis revealed a lymphatic malformation arising within a cystic oropharyngeal teratoma. Lymphatic malformations are virtually indistinguishable radiologically from rare, purely cystic teratomata, and efforts have been made to distinguish between the two in utero because of differing available treatment modalities. This represen

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16

International, Journal of Medical Science and Innovative Research (IJMSIR). "Decoding The Enigma: A Case Study on Oropharyngeal Synovial Sarcoma." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 6 (2024): 120–25. https://doi.org/10.5281/zenodo.15449089.

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<strong>Abstract</strong> Synovial sarcoma, a rare and aggressive subtype of sarcoma originating from mesenchymal cells, presents significant diagnostic and therapeutic challenges. This case report details an uncommon instance of synovial sarcoma located in the soft palate, a site with limited previous documentation. A 47-year-old male presented with a painless mass on the soft palate, initially suspected to be an abscess. This case underscores the necessity of considering malignancy in persistent or progressive soft tissue masses, even in atypical anatomical sites. Comprehensive diagnostic ev

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17

ALLIOUI, Soukaina, and M. Abdellaoui. "Aberrant internal carotids artery presenting as an oropharyngeal mass." International Journal of Case Reports and Images 11 (2020): 1. http://dx.doi.org/10.5348/101122z01sa2020cr.

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18

Johnson, Robert E., Kweon I. Stambaugh, Hunter Richmond, and Luis Balbuena. "Tortuous Internal Carotid Artery Presenting as an Oropharyngeal Mass." Otolaryngology–Head and Neck Surgery 112, no. 3 (1995): 479–82. http://dx.doi.org/10.1016/s0194-59989570290-3.

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19

JOHNSON, R., K. STAMBAUGH, H. RICHMOND, and L. BALBUENA. "Tortuous internal carotid artery presenting as an oropharyngeal mass." Otolaryngology - Head and Neck Surgery 112, no. 3 (1995): 479–82. http://dx.doi.org/10.1016/s0194-5998(95)70290-3.

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20

Wasserman, Jared M., Salvatore J. A. Sclafani, and Nira A. Goldstein. "Intraoperative evaluation of a pulsatile oropharyngeal mass during adenotonsillectomy." International Journal of Pediatric Otorhinolaryngology 70, no. 2 (2006): 371–75. http://dx.doi.org/10.1016/j.ijporl.2005.07.002.

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21

Rath, Rachna, ShadabAli Baig, and Tribikram Debata. "Rhinosporidiosis presenting as an oropharyngeal mass: A clinical predicament?" Journal of Natural Science, Biology and Medicine 6, no. 1 (2015): 241. http://dx.doi.org/10.4103/0976-9668.149207.

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22

Chung, Joseph Chun-Kit, and Wai-Kuen Ho. "A Large Cervical Osteophyte Presenting as an Oropharyngeal Mass." Ear, Nose & Throat Journal 90, no. 10 (2011): 476–78. http://dx.doi.org/10.1177/014556131109001005.

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23

Lim, Chee Chean, Tengku Ezulia, Qi Yi Bong, Halimuddin bin Sawali, and Anuar Idwan Idris. "Congenital Tuberculosis With Oropharyngeal Mass Presenting as Neonatal Stridor." JAMA Otolaryngology–Head & Neck Surgery 145, no. 9 (2019): 869. http://dx.doi.org/10.1001/jamaoto.2019.1708.

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24

Santana-Hernandez, D. J., S. R. Ell, P. Da Costa, C. P. Macklin, and S. S. M. Hussain. "Giant hamartoma of the oropharynx." Journal of Laryngology & Otology 110, no. 5 (1996): 480–82. http://dx.doi.org/10.1017/s0022215100134048.

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AbstractGiant polypoidal hamartomas of the pharynx and oesophagus are rare benign tumours of unknown origin, exceptionally arising from the oropharynx. We report the case of a 74-year-old man who developed sudden nausea and a foreign body sensation. Shortly afterwards he regurgitated a 25 × 3 × 1.5 cm pedunculated fleshy mass, still attached to the inside of his throat. The patient was anaesthetised, the mass traced to the right tonsillar fossa and adjacent oropharyngeal wall. The pedicle was clamped and the lesion excised. Histology was consistent with a giant oropharyngeal hamartoma. We disc

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25

Sergi, Bruno, Vittorio Alberti, Gaetano Paludetti, and Francesco Snider. "Extracranial internal carotid artery aneurysm presenting as pharyngeal mass with dysphagia." Journal of Laryngology & Otology 120, no. 2 (2005): 1–3. http://dx.doi.org/10.1017/s0022215105009795.

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Aneurysms of the extracranial portion of the internal carotid artery are rare. Generally, they occur just at the level of, or above, the bifurcation. Here we report a case of a left internal carotid artery aneurysm presenting as an oropharyngeal mass causing dysphagia.

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26

Alexander, Akash, Paul Mahoney, Emma Scurrell, and Stephen Baines. "Cholesteatoma in a cat." Journal of Feline Medicine and Surgery Open Reports 5, no. 1 (2019): 205511691984808. http://dx.doi.org/10.1177/2055116919848086.

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Case summary A 14-year-old neutered female Burmese cat was referred for investigation of a caudal oropharyngeal mass. CT showed a thin walled cyst-like structure filling and expanding from the right tympanic bulla. Histopathology showed fragments of mildly dysplastic squamous epithelium and aggregates of keratin. These findings were considered consistent with a diagnosis of cholesteatoma. Relevance and novel information To the best of our knowledge, this is the first reported case of a cholesteatoma in a cat. Cholesteatoma should be considered a differential diagnosis for cats presenting with

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27

Hilton, J. M., P. Tassone, J. Hanif, and B. Blagnys. "Anterior fracture dislocation of the odontoid peg in ankylosing spondylitis as a cause for rhinolalia clausa: a case study." Journal of Laryngology & Otology 122, no. 1 (2007): 105–7. http://dx.doi.org/10.1017/s0022215107007608.

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AbstractWe present an unusual cause of rhinolalia clausa secondary to an oropharyngeal mass. A 69-year-old male presented to the otorhinolaryngology clinic with a one year history of a ‘plummy’ voice. He had a longstanding history of severe ankylosing spondylitis. Examination revealed an obvious hyponasal voice and a smooth hard mass in the midline of the posterior nasopharyngeal and oropharyngeal walls. Subsequent computed tomography scans and lateral plain neck X-ray showed a fracture dislocation of the odontoid peg, secondary to ankylosing spondylitis, which had eroded through the body of t

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28

Bhinder, Prabhjot, Michael Chahin, and Lara Zuberi. "Concurrent Squamous Cell Carcinoma and Chronic Lymphocytic Leukemia Presenting as an Enlarging Neck Mass." Journal of Investigative Medicine High Impact Case Reports 7 (January 2019): 232470961984290. http://dx.doi.org/10.1177/2324709619842904.

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Chronic lymphocytic leukemia (CLL) patients are at an increased risk for developing more aggressive lymphomas via Richter’s transformation and of developing secondary malignancies. Despite the known association for secondary cancers, oropharyngeal cancers occur rarely. We present a case of a woman with a history of CLL who presented to our facility via transfer for impending airway compromise. Her initial workup was consistent with CLL; however, biopsies were taken of the neck mass because of its aggressive nature. She was treated with rituximab with good response. Final pathology showed evide

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29

Harpale, Puja, Megha Consul, Arun Kumar, and Anand Sinha. "A Rare Case of an Oropharyngeal Mass Causing Respiratory Distress." NeoReviews 26, no. 1 (2025): e53-e56. https://doi.org/10.1542/neo.26-1-009.

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30

Sareen, Rateesh, Menka Kapil, GN Gupta, and Anurag Govil. "Disseminated histoplasmosis in an immunocompetent individual presenting as oropharyngeal mass." International Journal of Oral Health Sciences 7, no. 1 (2017): 48. http://dx.doi.org/10.4103/ijohs.ijohs_6_17.

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31

Saleh, Husain A., Lewis Clayman, and Haitham Masri. "Fine needle aspiration biopsy of intraoral and oropharyngeal mass lesions." CytoJournal 5, no. 1 (2008): 4. http://dx.doi.org/10.1186/1742-6413-5-4.

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32

Hasan, Samiul, Nadia Afroz, and Jiaul Reza. "Tongue shaped oropharyngeal teratoma with cleft palate in a neonate: A case report." Journal of Neonatal Surgery 10 (February 23, 2021): 13. http://dx.doi.org/10.47338/jns.v10.929.

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Background: Atypical presentation of an atypical abnormality makes the diagnosis challenging. Oropharyngeal teratoma (epignathus) is a rare, potentially life-threatening neonatal tumor. Its atypical presentation may cause a delay in diagnosis and increase morbidity and mortality. Case presentation: A newborn girl with oropharyngeal teratoma and cleft palate presented with feeding difficulty. The airway was patent. The tumor was tongue-shaped, smooth-walled, displacing the native tongue, and prevented the fusion of two palatine halves resulting in cleft palate. On the 4th day of life, complete

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33

Ilyin, V. K., Z. O. Solovieva, O. A. Gizinger, et al. "Comparison of pcr diagnostic method and mass spectrometry of microbial markers method as applied to the evaluation of oral microbiota." Russian Clinical Laboratory Diagnostics 67, no. 8 (2022): 484–88. http://dx.doi.org/10.51620/0869-2084-2022-67-8-484-488.

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Rapid informative methods for assessing the species and quantitative composition of the microflora of the periodontal and oropharyngeal covering tissues are necessary for operative diagnostics, including those of the dentofacial system. The use of classical bacteriological methods, including seeding, incubation, counting and identification of microorganisms takes up to 5 days, resulting in a significant delay in obtaining the necessary information, which makes it difficult to carry out operative treatment measures. Therefore, the search for means and methods of operative microbiological contro

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34

Feraco, Paola, Emma Bragantini, Francesca Incandela, Cesare Gagliardo, and Marina Silvestrini. "Oropharyngeal Hairy Polyp: A Case of Respiratory Failure in a Newborn." Diagnostics 10, no. 7 (2020): 465. http://dx.doi.org/10.3390/diagnostics10070465.

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Hairy polyps, also known as dermoid polyps (DPs), are rare benign cystic lesions of bigerminal origin that may occur in several head and neck regions, including the oropharynx. Despite their benign histopathological nature, DPs may be life threatening, due to their upper airway location, and DPs represent one of the most unusual causes of respiratory distress during the neonatal period. In this paper, we describe a case of respiratory failure in a newborn with an oropharyngeal mass that was accidentally found during difficult intubation. Magnetic resonance imaging (MRI) detected a well-defined

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35

Hetterich, Johannes, Monica Mirolo, Franziska Kaiser, et al. "Concurrent Detection of a Papillomatous Lesion and Sequence Reads Corresponding to a Member of the Family Adintoviridae in a Bell’s Hinge-Back Tortoise (Kinixys belliana)." Animals 14, no. 2 (2024): 247. http://dx.doi.org/10.3390/ani14020247.

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An adult male Bell’s hinge-back tortoise (Kinixys belliana) was admitted to a veterinary clinic due to a swelling in the oral cavity. Physical examination revealed an approximately 2.5 × 1.5 cm sized, irregularly shaped tissue mass with villiform projections extending from its surface located in the oropharyngeal cavity. An initial biopsy was performed, and the lesion was diagnosed as squamous papilloma. Swabs taken for virological examination tested negative with specific PCRs for papillomavirus and herpesvirus. Further analysis of the oropharyngeal mass via metagenomic sequencing revealed se

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36

Yılmazer, Rasim. "A rare cause of oropharyngeal mass: bilateral aberrant internal carotid artery." Turkish Journal of Ear Nose and Throat 23, no. 6 (2013): 348–50. http://dx.doi.org/10.5606/kbbihtisas.2013.21548.

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37

Jain, Tarang, and Madhu Gupta. "Anesthetic management of an oropharyngeal mass: role of pre anesthetic assessment." Indian Journal of Clinical Anaesthesia 7, no. 1 (2020): 192–94. http://dx.doi.org/10.18231/j.ijca.2020.034.

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38

Wurlitzer, Marcus, Nikolaus Möckelmann, Malte Kriegs, et al. "Mass Spectrometric Comparison of HPV-Positive and HPV-Negative Oropharyngeal Cancer." Cancers 12, no. 6 (2020): 1531. http://dx.doi.org/10.3390/cancers12061531.

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Squamous cell carcinoma of the head and neck (HNSCC) consist of two distinct biological entities. While the numbers of classical, tobacco-induced HNSCC are declining, tumors caused by human papillomavirus (HPV) infection are increasing in many countries. HPV-positive HNSCC mostly arise in the oropharynx and are characterized by an enhanced sensitivity towards radiotherapy and a favorable prognosis. To identify molecular differences between both entities on the protein level, we conducted a mass spectrometric comparison of eight HPV-positive and nine HPV-negative oropharyngeal tumors (OPSCC). O

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39

Rickels, Michael R., Xiafang Zhang, Steven Mumm, and Michael P. Whyte. "Oropharyngeal Skeletal Disease Accompanying High Bone Mass and Novel LRP5 Mutation." Journal of Bone and Mineral Research 20, no. 5 (2004): 878–85. http://dx.doi.org/10.1359/jbmr.041223.

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40

Yanagisawa, Eiji, Stephen J. Salzer, and Ronald H. Hirokawa. "Endoscopic View of Antrochoanal Polyp Appearing as a Large Oropharyngeal Mass." Ear, Nose & Throat Journal 73, no. 10 (1994): 714–15. http://dx.doi.org/10.1177/014556139407301002.

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41

Durakovic, Nedim, Anand Rajan, and Nsangou Ghogomu. "Methotrexate-induced EBV-associated lymphoproliferative disorder presenting with an oropharyngeal mass." Human Pathology: Case Reports 10 (November 2017): 52–55. http://dx.doi.org/10.1016/j.ehpc.2016.11.003.

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42

Mullin, David, and Meredith Merz. "Case Report: A Branchial Cleft Anomaly Presenting as an Oropharyngeal Mass." Ear, Nose & Throat Journal 90, no. 12 (2011): 581–83. http://dx.doi.org/10.1177/014556131109001208.

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43

Mehta, Kinneri, Misha Movahed-Ezazi, and Akshay V. Patel. "Incidental Thyroid Mass in a Patient With Oropharyngeal Squamous Cell Carcinoma." JAMA Otolaryngology–Head & Neck Surgery 146, no. 9 (2020): 859. http://dx.doi.org/10.1001/jamaoto.2020.1616.

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44

Ferreira, Joana Maria Soares, Pedro Oliveira, Antonio Faria Almeida, and Artur Condé. "Oropharyngeal dysphagia as an uncommon manifestation of an osteoarticular disease." BMJ Case Reports 12, no. 1 (2019): e227411. http://dx.doi.org/10.1136/bcr-2018-227411.

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We report a case of a 76-year-old Caucasian woman who was referred to our department due to progressive dysphagia. We performed a flexible nasofibrolaryngoscopy that demonstrated the presence of a non-pulsatile mass in the right posterior wall of the hypopharynx. Cervical CT scan revealed that the mass represented a bulging of the hypopharynx wall produced by osteophytes along the cervical segment (C3–C4 and C4–C5) of the rachis. The patient was successfully treated with conservative measures with progressive improvement of dysphagia. This case highlights that anterior cervical osteophytosis s

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45

Made Gede Krisna Rendra Kawisana, I Wayan Sucipta, and I Putu Santhi Dewantara. "A Rare Manifestation of Metastatic Breast Cancer: Cervical Esophageal Stenosis with Oropharyngeal Dysphagia Decades After Primary Treatment." Open Access Indonesian Journal of Medical Reviews 5, no. 5 (2025): 1386–400. https://doi.org/10.37275/oaijmr.v5i5.767.

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Esophageal metastasis from breast cancer is an infrequent occurrence, with cervical esophageal involvement being exceptionally rare. Presentation with oropharyngeal dysphagia, particularly decades after primary breast cancer treatment, poses a significant diagnostic challenge. This report details such a case, emphasizing the clinical course and diagnostic complexities. A 60-year-old female, with a history of primary breast cancer treated approximately two decades prior and subsequent treatment for a locoregional recurrence with surgery, chemotherapy, and radiotherapy in 2019, presented with pr

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46

Răzniceanu, Mara, Ioana-Maria Calancea, and Monica Buzemurgă. "Synchronous Esophageal Squamous Cell Carcinoma And Oropharyngeal Carcinoma: Diagnosis And Management In A 45-Year-Old Patient." Journal of Medical and Radiation Oncology 4, no. 8 (2024): 54–60. https://doi.org/10.53011/jmro.2024.02.07.

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The occurrence of multiple primary cancers in patients is common. Esophageal squamous cell carcinoma (ESCC) may be associated with a second head and neck primary malignancy (HNSPM), which worsens prognosis. We describe here the case of a 54-year-old male with ESCC presenting as a tumor in the middle third of the thoracic esophagus, accompanied by progressive dysphagia and significant weight loss. A subsequent PET-CT revealed an oropharingeal mass that was confirmed by videofibroscopy and biopsy as a base of the tongue squamous cell carcinoma (SCC). Staging for both tumors after complete evalua

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47

O'Hara, Carolyn D., Michael W. Allegretto, Geoffrey D. Taylor, and Phillip A. Isotalo. "Epiglottic Histoplasmosis Presenting in a Nonendemic Region: A Clinical Mimic of Laryngeal Carcinoma." Archives of Pathology & Laboratory Medicine 128, no. 5 (2004): 574–77. http://dx.doi.org/10.5858/2004-128-574-ehpian.

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Abstract Histoplasma capsulatum is a dimorphic fungus endemic to North America. Histoplasmosis is primarily an inhalation-acquired mycosis that is encountered rarely outside of endemic regions. In nonendemic regions, histoplasmosis may present a diagnostic challenge and both clinical and laboratory vigilance are required to accurately identify infection. Unusual clinical presentations with limited physical findings may compound the difficulty in diagnosis. We describe a 78-year-old retired soil science professor who presented with an eroded epiglottic mass secondary to disseminated histoplasmo

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Mittal, Shweta, Madhu Priya, Saurabh Varshney, et al. "Atypical extra nasopharyngeal angiofibroma in an unusual location: tonsil posterior pillar (oropharynx)." European Journal of Clinical and Experimental Medicine 18, no. 1 (2020): 49–53. http://dx.doi.org/10.15584/ejcem.2020.1.11.

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Abstract:

Introduction. Angiofibroma is a benign, locally aggressive highly vascular tumor that typically affects young adolescent males and has a pathognomonic epicenter of origin in the nasopharynx. The atypical angiofibromas share the same histological features as that of Juvenile nasopharyngeal angiofibroma, however they differ significantly in their clinical features. Aim. Here we are reporting a very rare case of atypical angiofibroma in an adult male presenting as a non-vascular mass in the oropharynx with posterior pillar as the subsite. Description of the case. A 26-years old male patient prese

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Suporna, Saleh, Haque Sharmin, Mahmudul Huda Md., Shamim Farooq Md., Mizan Tazalle, and Mazharul Islam Kazi. "Common Malignant Tumour in Oral and Oropharyngral Lesion." INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND BIO-MEDICAL SCIENCE 05, no. 01 (2025): 18–21. https://doi.org/10.5281/zenodo.14615109.

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<strong>Background with Objective:</strong> A variety of non-neoplastic and neoplastic lesions can involve the oral cavity and oropharyngeal region. In 1971 WHO classified oral lesions into malignant tumours, benign tumours and tumor like lesions. The aim of this study was to assess the common types of malignant tumor in oral and oropharyngeal lesion.   <strong><em>Methods: </em></strong>This descriptive cross-sectional study was carried out among 98 patients presenting with malignant tumor in oral cavity and oropharynx at Pathology department for histopathology, Dhaka Medical C

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Low, Soon Khai, Clay T. Reed, Corina Millo, Evrim B. Turkbey, Jonathan Hernandez, and Charalampos S. Floudas. "Cecal mass: An unusual site of metastasis from HPV-associated oropharyngeal cancer." Oral Oncology 130 (July 2022): 105928. http://dx.doi.org/10.1016/j.oraloncology.2022.105928.

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