A Brief History of Head and Neck Pathology Developments☆,☆☆, Lester D.R
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Expression of P16ink4a Protein in Pleomorphic Adenoma And
Original research Ink4a Expression of p16 protein in pleomorphic J Clin Pathol: first published as 10.1136/jclinpath-2021-207440 on 3 May 2021. Downloaded from adenoma and carcinoma ex pleomorphic adenoma proves diversity of tumour biology and predicts clinical course Ewelina Bartkowiak ,1 Krzysztof Piwowarczyk,1 Magdalena Bodnar,1,2 Paweł Kosikowski,3 Jadzia Chou,1 Aldona Woźniak,3 Małgorzata Wierzbicka1 1Department of Otolaryngology ABSTRACT are an integral feature of PA; however, extensive and Laryngological Oncology, Aims The aim of the study is to correlate p16Ink4a squamous metaplasia is uncommon and can be Poznan University of Medical 7 Sciences, Poznan, Poland expression with the clinical courses of pleomorphic easily misinterpreted as squamous cell carcinoma. 2Department of Clinical adenoma (PA), its malignant transformation (CaexPA) In this paper, we present a new insight into a Pathomorphology, Nicolaus and treatment outcomes. single histological unit: PA. Our 20-year experi- Copernicus University in Toruń Methods Retrospective analysis (1998–2019) of 47 ence of 1500 PAs and extensive observation of their Ludwik Rydygier Collegium CaexPA, 148 PA and 22 normal salivary gland samples individually variable disease courses has prompted Medicum in Bydgoszcz, Bydgoszcz, Poland was performed. PAs were divided into two subsets: us to distinguish two clinically divergent subsets: 8 3Department of Clinical clinically ’slow’ tumours characterised by stable size or ‘fast’ and ‘slow’ tumours. While ‘fast’ PAs are Pathology, Poznan University slow growth; and ’fast’ tumours with rapid growth rate. characterised by a short medical history and rapid of Medical Sciences, Poznan, Results Positive p16Ink4a expression was found in growth, ‘slow’ PAs demonstrate very stable biology Poland 68 PA and 23 CaexPA, and borderline expression in and long- term growth. -
Primary Oncocytic Carcinoma of the Salivary Glands: a Clinicopathologic and Immunohistochemical Study of 12 Cases
Oral Oncology 46 (2010) 773–778 Contents lists available at ScienceDirect Oral Oncology journal homepage: www.elsevier.com/locate/oraloncology Primary oncocytic carcinoma of the salivary glands: A clinicopathologic and immunohistochemical study of 12 cases Chuan-Xiang Zhou a,1, Dian-Yin Shi b,1, Da-quan Ma b, Jian-guo Zhang b, Guang-Yan Yu b, Yan Gao a,* a Department of Oral Pathology, Peking University School and Hospital of Stomatology, Beijing 100081, PR China b Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, Beijing 100081, PR China article info summary Article history: Oncocytic carcinoma (OC) of salivary gland origin is an extremely rare proliferation of malignant onco- Received 31 May 2010 cytes with adenocarcinomatous architectural phenotypes, including infiltrative qualities. To help clarify Received in revised form 26 July 2010 the clinicopathologic and prognostic features of this tumor group, herein, we report 12 OC cases arising Accepted 27 July 2010 from the salivary glands, together with follow-up data and immunohistochemical observations. There Available online 16 September 2010 were 10 males and 2 females with an age range of 41 to 86 years (median age: 61.3 years). Most occurred in the parotid gland (10/12) with one in the palate and one in the retromolar gland. The tumors were Keywords: unencapsulated and often invaded into the nearby gland, lymphatic tissues and nerves. The neoplastic Oncocytic carcinoma cells had eosinophilic granular cytoplasm and round vesicular nuclei with prominent red nucleoli. Ultra- Salivary gland Clinicopathologic structural study, PTAH, and immunohistochemistry staining confirmed the presence of numerous mito- Immunohistochemistry chondria in the cytoplasm of oncocytes. -
First Description of a Hybrid Tumor of the Sublingual Gland
ANTICANCER RESEARCH 33: 4567-4572 (2013) First Description of a Hybrid Tumor of the Sublingual Gland WOLFGANG EICHHORN1, CLARISSA PRECHT1, MANFRED WEHRMANN2, ELISABETH HICKMANN2, MARC EICHHORN3, JÜRGEN ZEUCH3, THOMAS LÖNING4, REINHARD E. FRIEDRICH1, MAX HEILAND1 and JÜRGEN HOFFMANN5 1Department of Oral and Maxillofacial Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; 2Department of Pathology, General Hospital Nuertingen, Hamburg, Germany; 3Department of Oral and Maxillofacial Surgery, General Hospital, Balingen, Germany; 4Department of Pathology, Albertinen Hospital Hamburg, Hamburg, Germany; 5Department of Oral and Maxillofacial Surgery, Heidelberg University Hospital, Heidelberg, Germany Abstract. Background: Hybrid tumours of the salivary account for up to 0.1% of all salivary gland tumours, and glands are rare neoplasms. They are composed of at least both benign and malignant hybrid tumours have been two different tumour entities located in the same topographic reported. The prevalence is 0.4% among parotid gland area and account for only 0.1% of all salivary gland tumours (2). The most frequent tumour entities (Table I) are tumours. The most common component is an adenoid cystic adenoid cystic carcinoma, epithelial-myoepithelial carcinoma carcinoma. There are several possible forms of hybrid and salivary duct carcinoma, the combination of adenoid tumours, which are most commonly located in the parotid cystic carcinoma and epithelial-myoepithelial carcinoma gland. Case Report: We report on a 59-year-old female, who being the most common (1-10). presented with a lesion of the caruncula of the left sublingual To our knowledge, the hybrid tumour presented below is gland. The biopsy showed an adenoid cystic carcinoma in the first described for the sublingual gland. -
Clinical Radiation Oncology Review
Clinical Radiation Oncology Review Daniel M. Trifiletti University of Virginia Disclaimer: The following is meant to serve as a brief review of information in preparation for board examinations in Radiation Oncology and allow for an open-access, printable, updatable resource for trainees. Recommendations are briefly summarized, vary by institution, and there may be errors. NCCN guidelines are taken from 2014 and may be out-dated. This should be taken into consideration when reading. 1 Table of Contents 1) Pediatrics 6) Gastrointestinal a) Rhabdomyosarcoma a) Esophageal Cancer b) Ewings Sarcoma b) Gastric Cancer c) Wilms Tumor c) Pancreatic Cancer d) Neuroblastoma d) Hepatocellular Carcinoma e) Retinoblastoma e) Colorectal cancer f) Medulloblastoma f) Anal Cancer g) Epndymoma h) Germ cell, Non-Germ cell tumors, Pineal tumors 7) Genitourinary i) Craniopharyngioma a) Prostate Cancer j) Brainstem Glioma i) Low Risk Prostate Cancer & Brachytherapy ii) Intermediate/High Risk Prostate Cancer 2) Central Nervous System iii) Adjuvant/Salvage & Metastatic Prostate Cancer a) Low Grade Glioma b) Bladder Cancer b) High Grade Glioma c) Renal Cell Cancer c) Primary CNS lymphoma d) Urethral Cancer d) Meningioma e) Testicular Cancer e) Pituitary Tumor f) Penile Cancer 3) Head and Neck 8) Gynecologic a) Ocular Melanoma a) Cervical Cancer b) Nasopharyngeal Cancer b) Endometrial Cancer c) Paranasal Sinus Cancer c) Uterine Sarcoma d) Oral Cavity Cancer d) Vulvar Cancer e) Oropharyngeal Cancer e) Vaginal Cancer f) Salivary Gland Cancer f) Ovarian Cancer & Fallopian -
Laryngeal Cancer Survivorship
About the Authors Dr. Yadro Ducic MD completed medical school and Head and Neck Surgery training in Ottawa and Toronto, Canada and finished Facial Plastic and Reconstructive Surgery at the University of Minnesota. He moved to Texas in 1997 running the Department of Otolaryngology and Facial Plastic Surgery at JPS Health Network in Fort Worth, and training residents through the University of Texas Southwestern Medical Center in Dallas, Texas. He was a full Clinical Professor in the Department of Otolaryngology-Head Neck Surgery. Currently, he runs a tertiary referral practice in Dallas-Fort Worth. He is Director of the Baylor Neuroscience Skullbase Program in Fort Worth, Texas and the Director of the Center for Aesthetic Surgery. He is also the Codirector of the Methodist Face Transplant Program and the Director of the Facial Plastic and Reconstructive Surgery Fellowship in Dallas-Fort Worth sponsored by the American Academy of Facial Plastic and Reconstructive Surgery. He has authored over 160 publications, being on the forefront of clinical research in advanced head and neck cancer and skull base surgery and reconstruction. He is devoted to advancing the care of this patient population. For more information please go to www.drducic.com. Dr. Moustafa Mourad completed his surgical training in Head and Neck Surgery in New York City from the New York Eye and Ear Infirmary of Mt. Sinai. Upon completion of his training he sought out specialization in facial plastic, skull base, and reconstructive surgery at Baylor All Saints, under the mentorship and guidance of Dr. Yadranko Ducic. Currently he is based in New York City as the Division Chief of Head and Neck and Skull Base Surgery at Harlem Hospital, in addition to being the Director for the Center of Aesthetic Surgery in New York. -
Prognostic Significance of N-Cadherin Expression in Oral Squamous Cell Carcinoma
ANTICANCER RESEARCH 31: 4211-4218 (2011) Prognostic Significance of N-Cadherin Expression in Oral Squamous Cell Carcinoma M. DI DOMENICO1*, G.M. PIERANTONI2*, A. FEOLA1, F. ESPOSITO2, L. LAINO3, A. DE ROSA3, R. RULLO3, M. MAZZOTTA4, M. MARTANO4, F. SANGUEDOLCE5, L. PERILLO3, L. D’ANGELO6, S. PAPAGERAKIS7, S. TORTORELLA4, P. BUFO5, L. LO MUZIO4, G. PANNONE5 and A. SANTORO8 1Department of General Pathology, Second University of Naples, Naples, Italy; 2Department of Cellular and Molecular Biology and Pathology, Faculty of Medicine of Naples, University of Naples “Federico II”, Naples, Italy; 3Department of Oral Pathology, Orthodontics and Oral Surgery, Institute of Biochemistry, Second University of Naples, Naples, Italy; 4Department of Surgical Sciences - Section of Oral Pathology, University of Foggia, Foggia, Italy; 5Department of Surgical Sciences - Section of Anatomic Pathology and Cytopathology, University of Foggia, Foggia, Italy; 6Unit of Audiology, Head and Neck Surgery and Oncology, Second Univesity of Naples, Naples, Italy; 7Department of Otolaryngology, Head and Neck Surgery and Oncology, Medical School, University of Michigan Ann Arbor, Ann Arbor, MI, U.S.A.; 8Department of Anatomic Pathology, University of Bari, Bari, Italy Abstract. Background: N-Cadherin (CDH2) is a calcium- and only focal nuclear positivity was observed. Expression of dependent adhesion protein, whose de novo expression, re- cytoplasmic N-Cadherin correlated significantly with poor expression, up-regulation and down-regulation in human histological differentiation (p<0.05). Furthermore, we have tumors has been demonstrated. The aim of the present work observed significant a statistical trend for stage and a was to define the prognostic role of N-Cadherin in a large correlation with worst patient outcome, also confirmed by series of oral squamous cell carcinomas (OSCCs). -
CDHO Factsheet Oral Cancer
Disease/Medical Condition ORAL CANCER Date of Publication: August 7, 2014 (also known as “oral cavity cancer”) Is the initiation of non-invasive dental hygiene procedures* contra-indicated? Possibly (dental hygiene procedures should not be scheduled while the patient/client is experiencing oral ulcerations and pain, has an acute oral infection, has an absolute neutrophil count ≤ 1.0 X 109/L, or has a platelet count ≤ 50 X 109/L) Is medical consult advised? ..................................... Possibly (e.g., if suspicious lesion is detected; if intraoral infection and/or immunosuppression is suspected, particularly if the patient/client is undergoing radiation therapy and/or chemotherapy) Is the initiation of invasive dental hygiene procedures contra-indicated?** Possibly (contra-indicated for persons undergoing radiotherapy and/or chemotherapy for oral cancer); furthermore, dental hygiene procedures should not be scheduled while the patient/client is experiencing oral ulcerations and pain, has an acute oral infection, has an absolute neutrophil count ≤ 1000/mm3, or has a platelet count ≤ 50,000/mm3) Is medical consult advised? ...................................... See above. Is medical clearance required? .................................. Yes, if the patient/client is about to undergo or is undergoing active chemotherapy or radiation therapy for oral cancer. – Yes, if the patient/client is scheduled for major oral surgery for oral cancer. Is antibiotic prophylaxis required? ............................. No, not typically (although cancer or treatment-induced immunosuppression may warrant consideration of antibiotic prophylaxis). Is postponing treatment advised? .............................. Possibly (depends on whether cancer and its treatment may interfere with invasive procedures and whether there is immunosuppression associated with cancer treatment).1 Oral management implications Dental hygienists play an important role in early detection of oral cancer, leading to timely medical/dental referral and potential biopsy, endoscopy, and imaging. -
Head and Neck Squamous Cell Cancer and the Human Papillomavirus
MONOGRAPH HEAD AND NECK SQUAMOUS CELL CANCER AND THE HUMAN PAPILLOMAVIRUS: SUMMARY OF A NATIONAL CANCER INSTITUTE STATE OF THE SCIENCE MEETING, NOVEMBER 9–10, 2008, WASHINGTON, D.C. David J. Adelstein, MD,1 John A. Ridge, MD, PhD,2 Maura L. Gillison, MD, PhD,3 Anil K. Chaturvedi, PhD,4 Gypsyamber D’Souza, PhD,5 Patti E. Gravitt, PhD,5 William Westra, MD,6 Amanda Psyrri, MD, PhD,7 W. Martin Kast, PhD,8 Laura A. Koutsky, PhD,9 Anna Giuliano, PhD,10 Steven Krosnick, MD,4 Andy Trotti, MD,10 David E. Schuller, MD,3 Arlene Forastiere, MD,6 Claudio Dansky Ullmann, MD4 1 Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio. E-mail: [email protected] 2 Fox Chase Cancer Center, Philadelphia, Pennsylvania 3 Ohio State University Comprehensive Cancer Center, Columbus, Ohio 4 National Cancer Institute, Bethesda, Maryland 5 Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland 6 Johns Hopkins University School of Medicine, Baltimore, Maryland 7 Yale University School of Medicine, New Haven, Connecticut 8 University of Southern California, Los Angeles, California 9 University of Washington, Seattle, Washington 10 H. Lee Moffitt Cancer Center, Tampa, Florida Accepted 14 August 2009 Published online 29 September 2009 in Wiley InterScience (www.interscience.wiley.com). DOI: 10.1002/hed.21269 VC 2009 Wiley Periodicals, Inc. Head Neck 31: 1393–1422, 2009* Keywords: human papillomavirus; head and neck squamous Correspondence to: D. J. Adelstein cell cancer; state of the science Contract grant sponsor: NIH. Gypsyamber D’Souza is an advisory board member and received For the purpose of clinical trials, head and neck research funding from Merck Co. -
Oligometastatic HPV-Positive Oropharyngeal Cancer
Oligometastatic HPV-Positive Oropharyngeal Cancer Avinash R. Chaurasia1, Brandi R. Page2 1National Cancer Institute/National Capital Consortium, Bethesda, MD 2Johns Hopkins Medicine, Baltimore, MD December 2019 December 16, 2019 Learning Objectives • Follow-up of HPV+ Oropharyngeal (OP) H&N cancer patients • Patterns of failure of HPV+ OP cancer patients • Work-up of recurrent/metastatic HPV+ H&N cancer • Special considerations for oligometastatic HPV+ OP cancer December 16, 2019 Background • HPV+ OPSCC has a better prognosis than HPV- disease, but not treated significantly differently (subject of ongoing clinical trials) • Retrospective data suggests distant mets in HPV+ OPSCC significantly later than HPV- • HPV+ OPSCC have atypical patterns of failure December 16, 2019 Background • 11% of HPV+ OPSCC develop distant metastases – Majority (2/3) have polymetastatic disease, minority (1/3) have oligometastatic disease – Oligometastatic HPV+ OPSCC have been shown to have better OS than polymetastatic pts – Retrospective data point to two distinct populations: “indolent” phenotype and a “disseminated” phenotype • indolent have prolonged DFS and more likely to have oligomets December 16, 2019 Background • No clear treatment paradigm for metastatic HPV+ OPSCC pts: – Chemo ± immunotherapy • KEYNOTE-048: NCCN 3.2019 – PDL-1+: Pembrolizumab – PDL-1-: Pembro/cisplatin/5-FU • Checkmate 141 (~25% known HPV+) after progressing on cetuximab: benefit for nivolumab vs. investigator’s choice (2 yr OS 16.9% vs 6%) – Ablation/removal of metastatic sites (surgery vs stereotactic RT) December 16, 2019 Follow-up Paradigm • Currently same as HPV negative H&N cancer • H&P q1-3 months for 1 year, then q2-6 months for 1 year, then q4-8 months years 3-5 – Clinical oral exam and LN palpation, fiberoptic evaluation (NPL) • Imaging: PET/CT ≥ 12 weeks post-RT. -
Case Report Acinic Cell Carcinoma of Minor Salivary Gland of the Base of Tongue That Required Reconstructive Surgery
Hindawi Publishing Corporation Case Reports in Otolaryngology Volume 2012, Article ID 421065, 5 pages doi:10.1155/2012/421065 Case Report Acinic Cell Carcinoma of Minor Salivary Gland of the Base of Tongue That Required Reconstructive Surgery Kota Wada,1, 2 Subaru Watanabe,1 Yuji Ando,1 Yoichi Seino,2 and Hiroshi Moriyama2 1 Department of Otolaryngology, Asahi General Hospital, Chiba 289-2511, Japan 2 Department of Otorhinolaryngology—Head and Neck Surgery, Jikei University School of Medicine, Tokyo 105-8461, Japan Correspondence should be addressed to Kota Wada, [email protected] Received 2 October 2012; Accepted 14 November 2012 Academic Editors: H.-S. Lin, A. Rapoport, H. Sudhoff,A.Tas¸,andC.P.Wang Copyright © 2012 Kota Wada et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Acinic cell carcinoma of minor salivary gland of the base of tongue is very rare. Squamous cell carcinoma is the most common tumor in the base of tongue. We present a patient with gigantic acinic cell carcinoma of the base of tongue. This patient required emergency tracheotomy before surgery, because he had dyspnea when he came to our hospital. We removed this tumor by pull- through method and performed reconstructive surgery using a rectus abdominis myocutaneous flap. It was a case that to preserved movement of the tongue and swallowing function by keeping lingual arteries and hypoglossal nerves. This case was an extremely rare case of ACC of the base of tongue that required reconstructive surgery. -
Oral-Cancer-Facts-2020
Oral Cancer Facts • Slightly more than 53,000 Americans will be diagnosed with oral cancer in 2020. • Worldwide the problem is much greater, with new cases exceeding 640,000 annually. • In the US, approximately 132 new individuals each day will be diagnosed with oral cancer. • The fastest growing segment of the oral/oropharyngeal cancer population comes from HPV16, a virus that goes unnoticed with no precancerous signs. • Approximately one person every hour of every day 24/7/365 will die from oral cancer in the US alone. • While not related to biology, oral cancer occurs in blacks 2 to 1 over whites. • Oral cancer occurs in men 2 to 1 over women. Risk Factors • Tobacco use in all of its forms and alcohol are major risk factors for developing oral cancer. • While the vast majority of oral cancers (front/anterior of mouth) are related to tobacco and alcohol, about 10% of these cancers come from unknown causes. This includes all three types of cancers found in the oral environment: Squamous Cell Carcinoma (SCC), Adenoid Cystic Carcinoma (ACC), and Mucoepidermoid Carcinoma (MEC). • The unknown etiology cancers may arise from a genetic aberration or frailty or from a yet unidenti- fied common shared lifestyle risk factor. Signs and Symptoms • Any sore or ulceration that does not heal within 14 days. • A red, white, or black discoloration of the soft tissues of the mouth. • Any abnormality that bleeds easily when touched (friable). • A lump or hard spot in the tissue, usually border of the tongue (induration). • Tissue raised above that which surrounds it; a growth (exophytic). -
Head and Neck Pathology Traditional Prognostic Factors
314A ANNUAL MEETING ABSTRACTS Design: 421 archived cases of EC(1995-2007) were reviewed and TMAs prepared Conclusions: Positive GATA3 staining is seen in all vulvar PDs. GATA3 staining is as per established procedures. ERCC1 and RRM1 Immunofl uorescence stains were generally retained in the invasive component associated with vulvar PDs. GATA3 is combined with Automated Quantitative Analysis to assess their expression. The average more sensitive than GCDFP15 for vulvar PDs. Vulvar PDs only rarely express ER and of triplicate core expression was used to determine high and low score cutoff points PR. Vulvar PD should be added to the GATA3+/GCDFP15+ tumor list. using log-rank test on overall survival(OS). Association between expression profi les and clinicopathological parameters was tested using Fisher’s exact test. The independent prognostic value of ERCC1 and RRM1 was tested using Cox model adjusted for Head and Neck Pathology traditional prognostic factors. Results: 304(72%) type-I EC cases and 117(38%) type-II EC cases were identifi ed. Caucasian women had higher proportion of type-I tumors(p<0.001) while elderly women 1297 Subclassification of Perineural Invasion in Oral Squamous Cell were more likely to have type-II tumors (p<0.001). ERCC1 and RRM1 expression was Carcinoma: Prognostic Implications observed in 80% of tumors (336 cases 335 cases,respectively). Kaplan Meier curves K Aivazian, H Low, K Gao, JR Clark, R Gupta. Royal Prince Alfred Hospital, Sydney, showed statistically signifi cant difference in OS between low and high expression of New South Wales, Australia; Royal Prince Alfred Hospital, Sydney, Australia; Sydney ERCC1 and RRM1.