Disorders of Parotid Gland
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Glossary for Narrative Writing
Periodontal Assessment and Treatment Planning Gingival description Color: o pink o erythematous o cyanotic o racial pigmentation o metallic pigmentation o uniformity Contour: o recession o clefts o enlarged papillae o cratered papillae o blunted papillae o highly rolled o bulbous o knife-edged o scalloped o stippled Consistency: o firm o edematous o hyperplastic o fibrotic Band of gingiva: o amount o quality o location o treatability Bleeding tendency: o sulcus base, lining o gingival margins Suppuration Sinus tract formation Pocket depths Pseudopockets Frena Pain Other pathology Dental Description Defective restorations: o overhangs o open contacts o poor contours Fractured cusps 1 ww.links2success.biz [email protected] 914-303-6464 Caries Deposits: o Type . plaque . calculus . stain . matera alba o Location . supragingival . subgingival o Severity . mild . moderate . severe Wear facets Percussion sensitivity Tooth vitality Attrition, erosion, abrasion Occlusal plane level Occlusion findings Furcations Mobility Fremitus Radiographic findings Film dates Crown:root ratio Amount of bone loss o horizontal; vertical o localized; generalized Root length and shape Overhangs Bulbous crowns Fenestrations Dehiscences Tooth resorption Retained root tips Impacted teeth Root proximities Tilted teeth Radiolucencies/opacities Etiologic factors Local: o plaque o calculus o overhangs 2 ww.links2success.biz [email protected] 914-303-6464 o orthodontic apparatus o open margins o open contacts o improper -
Diseases of Salivary Glands: Review
ISSN: 1812–1217 Diseases of Salivary Glands: Review Alhan D Al-Moula Department of Dental Basic Science BDS, MSc (Assist Lect) College of Dentistry, University of Mosul اخلﻻضة امخجوًف امفموي تُئة رطبة، حتخوي ػىل طبلة ركِلة من امسائل ثدغى انوؼاب ثغطي امسطوح ادلاخوَة و متﻷ امفراغات تني ااطَة امفموًة و اﻷس نان. انوؼاب سائل مؼلد، ًنذج من امغدد انوؼاتَة، اذلي ًوؼة دورا" ىاما" يف اﶈافظة ػىل سﻻمة امفم. املرىض اذلٍن ؼًاهون من هلص يف اﻷفراز انوؼايب حكون دلهيم مشبلك يف اﻷلك، امخحدث، و امبوع و ًطبحون غرضة مﻷههتاابت يف اﻷغش َة ااطَة و امنخر املندرش يف اﻷس نان. ًوخد ثﻻثة أزواج من امغدد انوؼاتَة ام ئرُسة – امغدة امنكفِة، امغدة حتت امفكِة، و حتت انوساهَة، موضؼيا ٍكون خارج امخجوًف امفموي، يف حمفظة و ميخد هظاهما املنَوي مَفرغ افرازاهتا. وًوخد أًضا" امؼدًد من امغدد انوؼاتَة امطغرية ، انوساهَة، اتحنكِة، ادلىوزيًة، انوساهَة احلنكِة وما كبل امرخوًة، ٍكون موضؼيا مﻷسفل و مضن امغشاء ااطي، غري حماطة مبحفظة مع هجاز كنَوي كطري. افرازات امغدد انوؼاتَة ام ئرُسة مُست مدشاهبة. امغدة امفكِة ثفرز مؼاب مطيل غين ابﻷمِﻻز، وامغدة حتت امفكِة ثنذج مؼاب غين اباط، أما امغدة حتت انوساهَة ثنذج مؼااب" مزخا". ثبؼا" ميذه اﻷخذﻻفات، انوؼاب املوحود يق امفم ٌشار امَو مكزجي. ح كرَة املزجي انوؼايب مُس ثس َطا" واملادة اﻷضافِة اموػة من لك املفرزات انوؼاتَة، اكمؼدًد من امربوثُنات ثنذلل ثرسػة وثوخطق هبدروكس َل اﻷتُذاًت مﻷس نان و سطوح ااطَة امفموًة. ثبدأ أمراض امغدد انوؼاتَة ػادة تخغريات اندرة يف املفرزات و ام كرتَة، وىذه امخغريات ثؤثر اثهواي" من خﻻل جشلك انووحية اجلرثومِة و املوح، اميت تدورىا ثؤدي اىل خنور مذفش َة وأمراض وس َج دامعة. ىذه اﻷمراض ميكن أن ثطبح شدًدة تؼد املؼاجلة امشؼاغَة ﻷن امؼدًد من احلاﻻت اجليازًة )مثل امسكري، امخوَف اهكُيس( ثؤثر يف اجلراين انوؼايب، و ٌش خيك املرض من حفاف يف امفم. -
Heerfordt's Syndrome, Or Uveoparotid Fever
T h e new england journal o f medicine images in clinical medicine Lindsey R. Baden, M.D., Editor Heerfordt’s Syndrome, or Uveoparotid Fever A B C D Anisha Dua, M.D. 32-year-old woman presented with a 6-week history of swelling of both parotid glands, dry eyes, and dry mouth. She reported having difficulty West Penn Allegheny Health System Pittsburgh, PA A moving the right side of her face, and she felt tingling in the right side of her tongue. Physical examination revealed enlargement of both parotid glands, which were Augustine Manadan, M.D. firm and nontender, submandibular enlargement, and enlargement of lacrimal glands (Panel A). She did not have a fever, and there was no uveitis. She could not completely Rush University Medical Center Chicago, IL close her right eye, was unable to purse her lips, and was unable to smile on the right side of her face. Facial sensation was symmetric and intact. The results of a test for Lyme disease and the human immunodeficiency virus were negative. Serum IgG4 levels were normal. A chest radiograph suggested bilateral hilar adenopathy and possible right para tracheal adenopathy but was otherwise unremarkable. Computed tomography of the head revealed enlargement and increased uniform contrast enhancement of the both parotid glands (Panel B). A biopsy specimen from the right parotid gland revealed scattered granulomas with focal central necrosis. Stains for acid-fast bacilli and fungi were negative (Panel C, hematoxylin and eosin). She was given a diagnosis of Heer- fordt’s syndrome, a rare form of sarcoidosis in which the compression of the facial nerve results in palsy. -
Facial Nerve Disorders Cn7 (1)
FACIAL NERVE DISORDERS CN7 (1) Facial Nerve Disorders Last updated: January 18, 2020 FACIAL PALSY .......................................................................................................................................... 1 ETIOLOGY .............................................................................................................................................. 1 GUIDE TO LESION SITE LOCALIZATION ................................................................................................... 2 CLINICAL GRADING OF SEVERITY .......................................................................................................... 2 House-Brackmann grading scale ........................................................................................... 2 CLINICO-ANATOMICAL SYNDROMES ..................................................................................................... 2 Supranuclear (Central) Palsy ................................................................................................. 2 Nuclear Lesion ...................................................................................................................... 3 Cerebellopontine Angle Syndrome ....................................................................................... 3 Facial Canal Syndrome ......................................................................................................... 3 Stylomastoid Foramen Syndrome ........................................................................................ -
Lyme Disease Diagnostic Support Tool
1 / 11 For further details, click on the DIAGNOSTIC SUPPORT TOOL underlined words. Localized and disseminated stages of Lyme disease This diagnostic support tool is intended mainly for primary care clinicians. It is provided for information purposes only and should not replace the judgement of the clinician who performs the activities reserved under a statute or regulation. The recommendations in this tool were developed using a systematic process and are supported by the scientific literature and the knowledge and experience of Québec health professionals, experts and patients. For further details, go to the “Publications” section of INESSS’s website inesss.qc.ca. This tool does not deal with other tick-borne infections or with the much-debated form of Lyme disease, which is sometimes referred to as the chronic form. WHAT IS LYME DISEASE ? WHAT ARE THE DIFFERENT STAGES OF THE DISEASE? GENERAL INFORMATION • Lyme disease is an infectious disease caused by bacterial Localized stage (sometimes called the early stage): Beginning Patient with a tick genospecies of Borrelia burgdorferi, which are transmitted of the infection before dissemination of the bacteria in the • If tick is attached, refer to the procedure for removing it. to humans by black-legged ticks that are carriers. bloodstream. • Refer to the tick surveillance procedure. • Main manifestation observed: • It is a notifiable disease (MADO) • Consult the decision support tool or the Québec’s national and is on the increase in Québec. Not always present or noticed. medical protocol on post-exposure prophylaxis. • It can affect several anatomical systems at the same time. If present, usually appears • Identifying the tick and obtaining proof that it carries of Lym 3 to 30 days after infection or e d B. -
Practice Parameter for the Diagnosis and Management of Primary Immunodeficiency
Practice parameter Practice parameter for the diagnosis and management of primary immunodeficiency Francisco A. Bonilla, MD, PhD, David A. Khan, MD, Zuhair K. Ballas, MD, Javier Chinen, MD, PhD, Michael M. Frank, MD, Joyce T. Hsu, MD, Michael Keller, MD, Lisa J. Kobrynski, MD, Hirsh D. Komarow, MD, Bruce Mazer, MD, Robert P. Nelson, Jr, MD, Jordan S. Orange, MD, PhD, John M. Routes, MD, William T. Shearer, MD, PhD, Ricardo U. Sorensen, MD, James W. Verbsky, MD, PhD, David I. Bernstein, MD, Joann Blessing-Moore, MD, David Lang, MD, Richard A. Nicklas, MD, John Oppenheimer, MD, Jay M. Portnoy, MD, Christopher R. Randolph, MD, Diane Schuller, MD, Sheldon L. Spector, MD, Stephen Tilles, MD, Dana Wallace, MD Chief Editor: Francisco A. Bonilla, MD, PhD Co-Editor: David A. Khan, MD Members of the Joint Task Force on Practice Parameters: David I. Bernstein, MD, Joann Blessing-Moore, MD, David Khan, MD, David Lang, MD, Richard A. Nicklas, MD, John Oppenheimer, MD, Jay M. Portnoy, MD, Christopher R. Randolph, MD, Diane Schuller, MD, Sheldon L. Spector, MD, Stephen Tilles, MD, Dana Wallace, MD Primary Immunodeficiency Workgroup: Chairman: Francisco A. Bonilla, MD, PhD Members: Zuhair K. Ballas, MD, Javier Chinen, MD, PhD, Michael M. Frank, MD, Joyce T. Hsu, MD, Michael Keller, MD, Lisa J. Kobrynski, MD, Hirsh D. Komarow, MD, Bruce Mazer, MD, Robert P. Nelson, Jr, MD, Jordan S. Orange, MD, PhD, John M. Routes, MD, William T. Shearer, MD, PhD, Ricardo U. Sorensen, MD, James W. Verbsky, MD, PhD GlaxoSmithKline, Merck, and Aerocrine; has received payment for lectures from Genentech/ These parameters were developed by the Joint Task Force on Practice Parameters, representing Novartis, GlaxoSmithKline, and Merck; and has received research support from Genentech/ the American Academy of Allergy, Asthma & Immunology; the American College of Novartis and Merck. -
Classification of Salivary Gland Disorders
Salivary Gland Diseases and Disorders Dr. Mahmoud E. Khalifa Prof of OMFS Lecture ILOs At the end of this chapter you should be able to: 1. Distinguish the clinical features of infections of the salivary glands from those in other structures 2. Differentiate on clinical grounds between infection, obstruction, benign and malignant neoplasms of the salivary glands 3. Plan and evaluate the results of the investigation of disorders of the salivary glands 4. List the important/relevant information to be elicited from patients with salivary gland disorders 5. Select cases which require referral for a specialist opinion 6. Describe the causes of a dry mouth and be able to distinguish between organic and functional causes. Anatomy Major glands Minor glands 3 pairs Situated mostly 800 to 1000 in the oral cavity Parotid Submandibular The majority atAlso found in the the junction of pharynx, larynx, the hard and soft trachea, and palates sinuses sublingual Functions These glands function to produce saliva, which serves as Lubricant for speech & swallowing Assists taste Immunologic (antibacterial) Digestive Cleansing properties Based on the type of secretion, the salivary glands may be grouped as: (i) Serous, (ii) Mucous and (iii) Mixed. Parotid gland secretion is serous in nature. The sublingual gland secretes mixed, but predominantly mucous. The submandibular gland secretion is also mixed, but is predominantly serous. The minor glands secrete mucous saliva. Parotid Gland The parotid gland is the largest salivary gland, the secretion of which is serous in nature. It is pyramidal in shape; The base located superficial and apex medially The base is triangular in shape its apex is towards the angle of the mandible, the base at the external acoustic meatus The parotid duct (Stenson‘s duct) Emerges at the anterior part of the gland. -
Chapter 11. Non-Neoplastic Diseases of Salivary Glands
Surgical pathology of the mouth and jaws R. A. Cawson, J. D. Langdon, J. W. Eveson 11. Non-neoplastic diseases of salivary glands Investigation Investigations will be discussed in relation to specific disorders and those more appropriate to neoplasms are discussed in the following chapter. However, it must be emphasized that chronic inflammatory swellings of the major salivary glands, in particular, sometimes cannot be distinguished from neoplasms clinically. Nevertheless, biopsy of the parotid glands is contraindicated because of the frequency of pleomorphic adenomas which can be seeded into the surrounding tissues to produce multiple recurrences. There are also the risks of damaing branches of the facial nerve or of producing a parotid fistula. For imaging techniques, see Chapters 1 and 12. Developmental disorders Aplasia/agenesis. Complete absence of one or more salivary glands is very rare, but occasionally the parotid glands are absent. Absence of all major salivary glands is even more rare. Duct atresia. This is also rare, but usually affects the submandibular duct in the floor of the mouth. Absence of the duct results in retention cysts of the submandibular and sublingual glands. Salivary gland hypoplasia. This can be a feature of the Melkersson-Rosenthal syndrome. The hypoplasia possibly may be secondary to atrophy of parasympathetic nerves thought to be implicated in this syndrome. Congenital salivary fistulae. These are sometimes seen in association with branchial clefts. Aberrant salivary tissue. This is common in the cervical lymph nodes (where it should not be mistaken for a metastasis) and may be found in the middle ear cleft. Stafne's bone cavity is another example. -
Heerfordt-Waldenstrom Syndrome Uveoparotid Fever
Case Report Heerfordt-Waldenstrom Syndrome Pak Armed Forces Med J 2015; 65(5): 716-17 HEERFORDT-WALDENSTROM SYNDROME UVEOPAROTID FEVER: REVIEW OF THE LITERATURE AND A CASE PRESENTATION Kamil Shujaat, Aysha Babar*, Maryam Rashid**, Syed Saif Ur Rehman, Shujaat Hussain Al-Nafees Medical College Islamabad Pakistan, *Yusra Medical and Dental College Islamabad Pakistan, **Akhtar Saeed Medical and Dental College Lahore Pakistan ABSTRACT Heerfordt-Waldenström syndrome is also referred to as uveoparotid fever. In our patient physical examination showed bilateral parotid gland enlargement. Chest X-ray showed bilateral hilar lymph adenopathy. Biopsy specimen from the right parotid gland revealed scattered granulomas with focal central necrosis. Stains for acid-fast bacilli and fungi were negative. He was diagnosed as a case of Heerfordt- Waldenström syndrome, a rare form of sarcoidosis in which the compression of the facial nerve results in palsy. He was treated with 60 mg of prednisone daily, and at follow-up after two weeks later, the swelling and uveitis was resolved. Keywords: Heerfordt-waldenstrom syndrome, Uveoparotid fever. INTRODUCTION calcium was 9.7 mg /dl. X-ray chest (PA) view showed bilateral hilar lymphadenopathy (fig-2). Heerfordt syndrome also called as Fine needle aspiration of parotid gland revealed uveoparotid fever is a rare type of sarcoidosis which presents with fever, uveitis, parotid gland enlarement and cranial nerve palsies most commonly facial nerve1. In 1909, the condition was first described by Danish ophthalmologist Christian Frederick Heerfordt, for whom the syndrome is now named2. CASE REPORT We report a case of 24 years old student who presented with 2 weeks history of fever, cough, and facial palsy, difficulty in swallowing and blurred vision (fig-1). -
Sarcoidosis (Heerfordt Syndrome): a Case Report Tiia Tamme, Edvitar Leibur, Andres Kulla
REVIEW Stomatologija, Baltic Dental and Maxillofacial Journal, 9:61-64, 2007 Sarcoidosis (Heerfordt syndrome): A case report Tiia Tamme, Edvitar Leibur, Andres Kulla SUMMARY We report the case of a 22-year-old woman who is suspected of having primary Sjögren´s syndrome. She complaining of bilateral swelling of eyelids and the parotid glands of three weeks duration. Physical examination revealed a bilateral enlargement of both parotid glands, which were solid and painful. Sjögren´s syndrome was suspected at that stage, and the serologic and specific analysis were done. All these tests didn´t find any autoimmune or visceral features typical of Sjögren´s syndrome and autoantibodies were negative. During follow-up time the right facial nerve palsy de- veloped. Pulmonary radiography revealed bihilar lymphadenopathy and labial salivary gland biopsy revealed non-caseating granuloma. The patient was classified as having stage I sarcoidosis. This case demonstrates the importance of being aware of the leading clinical signs and symptoms in case of Heerfordt syndrome. Key words: Sjögren syndrome, sarcoidosis, Heerfordt syndrome. INTRODUCTION Sarcoidosis is a condition characterized by multiple appear to have the highest prevalence rates in the world nodular lesions in the skin, internal organs, eyes, sali- [7]. vary glands, and with enlargement of lymphnodes [1]. Geographic and environmental factors may explain Danish ophthalmologist C. F. Heerfordt first described differences between countries and age groups [8]. the symptom triad – uveitis, parotid gland enlargement An abnormal immune response to a yet unidenti- and cranial nerve paresis in 1909 [2]. Sarcoidosis rep- fied antigen is suspected as the cause. resents a granulomatous disease of obscure etiology. -
Treatments for Ankyloglossia and Ankyloglossia with Concomitant Lip-Tie Comparative Effectiveness Review Number 149
Comparative Effectiveness Review Number 149 Treatments for Ankyloglossia and Ankyloglossia With Concomitant Lip-Tie Comparative Effectiveness Review Number 149 Treatments for Ankyloglossia and Ankyloglossia With Concomitant Lip-Tie Prepared for: Agency for Healthcare Research and Quality U.S. Department of Health and Human Services 540 Gaither Road Rockville, MD 20850 www.ahrq.gov Contract No. 290-2012-00009-I Prepared by: Vanderbilt Evidence-based Practice Center Nashville, TN Investigators: David O. Francis, M.D., M.S. Sivakumar Chinnadurai, M.D., M.P.H. Anna Morad, M.D. Richard A. Epstein, Ph.D., M.P.H. Sahar Kohanim, M.D. Shanthi Krishnaswami, M.B.B.S., M.P.H. Nila A. Sathe, M.A., M.L.I.S. Melissa L. McPheeters, Ph.D., M.P.H. AHRQ Publication No. 15-EHC011-EF May 2015 This report is based on research conducted by the Vanderbilt Evidence-based Practice Center (EPC) under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. 290-2012-00009-I). The findings and conclusions in this document are those of the authors, who are responsible for its contents; the findings and conclusions do not necessarily represent the views of AHRQ. Therefore, no statement in this report should be construed as an official position of AHRQ or of the U.S. Department of Health and Human Services. The information in this report is intended to help health care decisionmakers—patients and clinicians, health system leaders, and policymakers, among others—make well-informed decisions and thereby improve the quality of health care services. This report is not intended to be a substitute for the application of clinical judgment. -
Heerfordt-Waldenström Syndrome Manifesting As Cardiac Sarcoidosis
Open Access Case Report DOI: 10.7759/cureus.10619 Heerfordt-Waldenström Syndrome Manifesting as Cardiac Sarcoidosis Sebastian Mikulic 1 , Pujan Patel 2 , Sandra Sheffield 1 , Fadi Kandah 1 , Gladys Velarde 2 1. Internal Medicine, University of Florida Health Jacksonville, Jacksonville, USA 2. Cardiology, University of Florida Health Jacksonville, Jacksonville, USA Corresponding author: Sebastian Mikulic, [email protected] Abstract Sarcoidosis is a granulomatous disease histologically characterized by non-caseating granulomas. Although it usually affects the lungs, it can affect any organ system and present with a wide variety of symptoms. Heerfordt-Waldenström Syndrome, or uveoparotid fever, is a rare form of sarcoidosis that presents with a combination of fever, parotitis, facial paralysis, and uveitis. In this case report, we demonstrate a rare manifestation of sarcoidosis in a patient who presents with both the aforementioned syndrome and cardiac involvement. This case serves to highlight the importance of identifying the various clinical manifestations and management of systemic sarcoidosis. Categories: Cardiology, Internal Medicine, Rheumatology Keywords: heerfordt-waldenström syndrome, uveoparotid fever, sarcoidosis, cardiac sarcoidosis Introduction Sarcoidosis is a multi-organ inflammatory disease of unknown etiology. It is characterized by the deposition of non-caseating granulomas in various tissues, and patients are generally diagnosed early in adulthood, usually before the age of 50. The incidence and prevalence of sarcoidosis are highest in African Americans. The disease can affect multiple organ systems: musculoskeletal, respiratory, ocular, cardiovascular, gastrointestinal, lymphatic, and neurological systems [1]. Heerfordt-Waldenström syndrome is a rare presentation of sarcoidosis. First described by Dr. Christian Heerfordt in the early 1900s, and later connected to sarcoidosis by Dr.