Casefinding Code List for Reportable Tumors (Effective 10/1/2015)
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Disease Discovery Classification of Lymphoid Neoplasms
From www.bloodjournal.org by on December 4, 2008. For personal use only. 2008 112: 4384-4399 doi:10.1182/blood-2008-07-077982 Classification of lymphoid neoplasms: the microscope as a tool for disease discovery Elaine S. Jaffe, Nancy Lee Harris, Harald Stein and Peter G. Isaacson Updated information and services can be found at: http://bloodjournal.hematologylibrary.org/cgi/content/full/112/12/4384 Articles on similar topics may be found in the following Blood collections: Neoplasia (4200 articles) Free Research Articles (544 articles) ASH 50th Anniversary Reviews (32 articles) Clinical Trials and Observations (2473 articles) Information about reproducing this article in parts or in its entirety may be found online at: http://bloodjournal.hematologylibrary.org/misc/rights.dtl#repub_requests Information about ordering reprints may be found online at: http://bloodjournal.hematologylibrary.org/misc/rights.dtl#reprints Information about subscriptions and ASH membership may be found online at: http://bloodjournal.hematologylibrary.org/subscriptions/index.dtl Blood (print ISSN 0006-4971, online ISSN 1528-0020), is published semimonthly by the American Society of Hematology, 1900 M St, NW, Suite 200, Washington DC 20036. Copyright 2007 by The American Society of Hematology; all rights reserved. From www.bloodjournal.org by on December 4, 2008. For personal use only. ASH 50th anniversary review Classification of lymphoid neoplasms: the microscope as a tool for disease discovery Elaine S. Jaffe,1 Nancy Lee Harris,2 Harald Stein,3 and Peter -
LIST of OCCUPATIONAL DISEASES (Revised 2010)
LIST OF OCCUPATIONAL DISEASES (revised 2010) Identification and recognition of occupational diseases: Criteria for incorporating diseases in the ILO list of occupational diseases Occupational Safety and Health Series, No. 74 List of occupational diseases (revised 2010) Identification and recognition of occupational diseases: Criteria for incorporating diseases in the ILO list of occupational diseases INTERNATIONAL LABOUR OFFICE • GENEVA Copyright © International Labour Organization 2010 First published 2010 Publications of the International Labour Office enjoy copyright under Protocol 2 of the Universal Copyright Convention. Nevertheless, short excerpts from them may be reproduced without authorization, on condition that the source is indicated. For rights of reproduction or translation, application should be made to ILO Publications (Rights and Permissions), International Labour Office, CH-1211 Geneva 22, Switzerland, or by email: pubdroit@ ilo.org. The International Labour Office welcomes such applications. Libraries, institutions and other users registered with reproduction rights organizations may make copies in accordance with the licences issued to them for this purpose. Visit www.ifrro.org to find the reproduction rights organization in your country. ILO List of occupational diseases (revised 2010). Identification and recognition of occupational diseases: Criteria for incorporating diseases in the ILO list of occupational diseases Geneva, International Labour Office, 2010 (Occupational Safety and Health Series, No. 74) occupational disease / definition. 13.04.3 ISBN 978-92-2-123795-2 ISSN 0078-3129 Also available in French: Liste des maladies professionnelles (révisée en 2010): Identification et reconnaissance des maladies professionnelles: critères pour incorporer des maladies dans la liste des maladies professionnelles de l’OIT (ISBN 978-92-2-223795-1, ISSN 0250-412x), Geneva, 2010, and in Spanish: Lista de enfermedades profesionales (revisada en 2010). -
ICD-10 International Statistical Classification of Diseases and Related Health Problems
ICD-10 International Statistical Classification of Diseases and Related Health Problems 10th Revision Volume 2 Instruction manual 2010 Edition WHO Library Cataloguing-in-Publication Data International statistical classification of diseases and related health problems. - 10th revision, edition 2010. 3 v. Contents: v. 1. Tabular list – v. 2. Instruction manual – v. 3. Alphabetical index. 1.Diseases - classification. 2.Classification. 3.Manuals. I.World Health Organization. II.ICD-10. ISBN 978 92 4 154834 2 (NLM classification: WB 15) © World Health Organization 2011 All rights reserved. Publications of the World Health Organization are available on the WHO web site (www.who.int) or can be purchased from WHO Press, World Health Organization, 20 Avenue Appia, 1211 Geneva 27, Switzerland (tel.: +41 22 791 3264; fax: +41 22 791 4857; e-mail: [email protected]). Requests for permission to reproduce or translate WHO publications – whether for sale or for noncommercial distribution – should be addressed to WHO Press through the WHO web site (http://www.who.int/about/licensing/copyright_form). The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. -
FAQ REGARDING DISEASE REPORTING in MONTANA | Rev
Disease Reporting in Montana: Frequently Asked Questions Title 50 Section 1-202 of the Montana Code Annotated (MCA) outlines the general powers and duties of the Montana Department of Public Health & Human Services (DPHHS). The three primary duties that serve as the foundation for disease reporting in Montana state that DPHHS shall: • Study conditions affecting the citizens of the state by making use of birth, death, and sickness records; • Make investigations, disseminate information, and make recommendations for control of diseases and improvement of public health to persons, groups, or the public; and • Adopt and enforce rules regarding the reporting and control of communicable diseases. In order to meet these obligations, DPHHS works closely with local health jurisdictions to collect and analyze disease reports. Although anyone may report a case of communicable disease, such reports are submitted primarily by health care providers and laboratories. The Administrative Rules of Montana (ARM), Title 37, Chapter 114, Communicable Disease Control, outline the rules for communicable disease control, including disease reporting. Communicable disease surveillance is defined as the ongoing collection, analysis, interpretation, and dissemination of disease data. Accurate and timely disease reporting is the foundation of an effective surveillance program, which is key to applying effective public health interventions to mitigate the impact of disease. What diseases are reportable? A list of reportable diseases is maintained in ARM 37.114.203. The list continues to evolve and is consistent with the Council of State and Territorial Epidemiologists (CSTE) list of Nationally Notifiable Diseases maintained by the Centers for Disease Control and Prevention (CDC). In addition to the named conditions on the list, any occurrence of a case/cases of communicable disease in the 20th edition of the Control of Communicable Diseases Manual with a frequency in excess of normal expectancy or any unusual incident of unexplained illness or death in a human or animal should be reported. -
15 Hereditary Renal Cancer
Hereditary Renal Cancer 239 15 Hereditary Renal Cancer Toshiyuki Miyazaki and Mutsumasa Takahashi CONTENTS 15.1 Introduction 15.1 Introduction 239 15.2 Histologic Subtypes of Renal Cancer 240 15.3 von Hippel-Lindau Disease 241 Renal cancer is diagnosed in over 30,000 Ameri- 15.3.1 Clinical Features 241 cans each year, accounting for approximately 15.3.2 Genetics 243 12,000 deaths annually. Smoking, obesity, and occu- 15.3.3 Imaging and Management 243 pational exposure have been implicated in the devel- 15.4 Hereditary Papillary Renal Cancer 248 opment of renal cancers but, in general, their cause 15.4.1 Clinical Features 248 Moyad 15.4.2 Genetics 248 remains obscure ( 2001). Although heredi- 15.4.3 Imaging and Management 249 tary renal cancer makes up only about 4% of the 15.5 Hereditary Leiomyoma Renal Cell Carcinoma 249 total number of cases, this percentage is expected 15.5.1 Clinical Features 249 to increase as a more complete understanding of 15.5.2 Genetics 250 the genetic causes of cancer is elucidated (Gago- 15.5.3 Imaging and Management 250 Dominguez 15.6 Birt-Hogg-Dubé Syndrome 251 et al. 2001). 15.6.1 Clinical Features 251 Increasing knowledge of hereditary renal cancer 15.6.2 Genetics 251 syndromes has provided insights into the mecha- 15.6.3 Imaging and Management 251 nisms of cancer development in the general popula- 15.7 Familial Renal Oncocytoma 252 tion and has assisted efforts to prevent and treat renal 15.7.1 Clinical Features 252 cancers. These cancers include von Hippel-Lindau 15.7.2 Genetics 252 15.7.3 Imaging and Management 252 disease, hereditary papillary renal cancer, hereditary 15.8 Medullary Carcinoma of Kidney 253 leiomyoma renal cell carcinoma, Birt-Hogg-Dubé 15.8.1 Clinical Features 253 syndrome, hereditary renal oncocytoma, familial 17.8.2 Genetics 253 renal oncocytoma, medullary carcinoma of kidney, 17.8.3 Imaging and Management 253 and tuberous sclerosis (Table 15.1; Choyke at al. -
History of the Statistical Classification of Diseases and Causes of Death
Copyright information All material appearing in this report is in the public domain and may be reproduced or copied without permission; citation as to source, however, is appreciated. Suggested citation Moriyama IM, Loy RM, Robb-Smith AHT. History of the statistical classification of diseases and causes of death. Rosenberg HM, Hoyert DL, eds. Hyattsville, MD: National Center for Health Statistics. 2011. Library of Congress Cataloging-in-Publication Data Moriyama, Iwao M. (Iwao Milton), 1909-2006, author. History of the statistical classification of diseases and causes of death / by Iwao M. Moriyama, Ph.D., Ruth M. Loy, MBE, A.H.T. Robb-Smith, M.D. ; edited and updated by Harry M. Rosenberg, Ph.D., Donna L. Hoyert, Ph.D. p. ; cm. -- (DHHS publication ; no. (PHS) 2011-1125) “March 2011.” Includes bibliographical references. ISBN-13: 978-0-8406-0644-0 ISBN-10: 0-8406-0644-3 1. International statistical classification of diseases and related health problems. 10th revision. 2. International statistical classification of diseases and related health problems. 11th revision. 3. Nosology--History. 4. Death- -Causes--Classification--History. I. Loy, Ruth M., author. II. Robb-Smith, A. H. T. (Alastair Hamish Tearloch), author. III. Rosenberg, Harry M. (Harry Michael), editor. IV. Hoyert, Donna L., editor. V. National Center for Health Statistics (U.S.) VI. Title. VII. Series: DHHS publication ; no. (PHS) 2011- 1125. [DNLM: 1. International classification of diseases. 2. Disease-- classification. 3. International Classification of Diseases--history. 4. Cause of Death. 5. History, 20th Century. WB 15] RB115.M72 2011 616.07’8012--dc22 2010044437 For sale by the U.S. -
Attachment D: Selection and Assignment of Oasis Diagnosis
ATTACHMENT D: SELECTION AND ASSIGNMENT OF OASIS DIAGNOSIS A. INTRODUCTION Attachment D was initially published to facilitate the introduction of V-code diagnosis reporting on the OASIS, (see OASIS-B1, 12/2002), effective October 1, 2003. The attachment was designed to clarify HHA implementation of the Official ICD-9-C M Coding Guidelines of 2002. The changes in OASIS diagnosis reporting in 2003 allowed HHAs the ability to assign V-codes to M0230 and M0240 and comply with the provisions of the Health Insurance Portability and Accountability Act (HIPAA, Title II). We are reissuing this document to promote accurate selection and assignment of the patient’s diagnosis on the current OASIS (OASIS B1 (1/2008). This document addresses the OASIS diagnoses items that pertain to the home health episode (i.e., M0230, M0240 and M0246) and will clarify CMS’ expectations specific to the assignment of V-codes to the OASIS as dictated by the revised ICD-9-C M coding guidelines effective October 2008. Additionally, with (HH PPS) refinements in January 2008, the HH PPS grouper was revised. If a V-code assigned to M0230/240 replaces a case mix diagnosis code, HHAs no longer must always code a numeric diagnosis code in the optional case mix diagnosis (M0246). ICD-9-C M coding guidelines state that certain rehabilitation and aftercare V-codes need a secondary diagnosis code in M0240 to describe a resolving condition or sequelae. If the diagnoses codes representing the underlying condition displaced by the V-code are case mix codes, the HH PPS grouper will look to M0240 to award appropriate points. -
Endometriosis in Australia: Prevalence and Hospitalisations (Report)
Endometriosis in Australia: prevalence and hospitalisations Published August 2019 Around 1 in 9 women born in 1973–78 were diagnosed Endometriosis is a chronic condition that can be painful, with endometriosis by age 40–44 affect fertility and lead to reduced participation in school, work and sporting activities. The condition cost an estimated $7.4 billion in Australia in 2017–18, mostly through reduced quality of life and productivity losses (Ernst & Young 2019). This may be an underestimate, however, due to difficulties in diagnosing endometriosis There were around 34,200 and underdiagnosis. endometriosis-related hospitalisations in 2016–17 What is endometriosis? Endometriosis occurs when endometrial-like tissue, similar to the tissue normally found lining the uterus, is found in other parts of the body, such as the ovaries, fallopian tubes, peritoneum (the membrane lining the abdominal and pelvic cavities) and the outside of the uterus. These tissues are collectively known as endometriosis Nearly 4 in 5 (79%) and, like the endometrial tissue lining the uterus, they respond to endometriosis-related hormones released by the ovaries, causing bleeding. This leads hospitalisations in 2016–17 were among females to inflammation and scarring, which can cause painful ‘adhesions’ aged 15–44 joining together pelvic organs which are normally separate. The causes of endometriosis are unclear, but factors that seem to increase the risk of endometriosis include a family history of endometriosis and menstrual cycle factors such as early age at first period, short menstrual cycles, and heavy or long periods (Jean Hailes for Women’s Health 2017b). Around 15 of every Some people with endometriosis experience no symptoms; others 1,000 hospitalisations among may experience pain, heavy menstrual bleeding, bleeding between females aged 15–44 in 2016–17 periods, lethargy and reduced fertility, among other symptoms. -
The Spectrum of Autoimmune Diseases
Sarah Ballantyne, PhD 1717 The Spectrum of Autoimmune Diseases The following is a list of diseases that are either confirmed autoimmune diseases or for which there is very strong scientific evidence for autoimmune origins: Acute brachial neuropathy (also Atrophic polychondritis (also known Besnier-Boeck disease (also known A known as acute brachial radiculitis, as systemic chondromalacia and as sarcoidosis) neuralgic amyotrophy, brachial relapsing polychondritis) Bickerstaff’s encephalitis neuritis, brachial plexus neuropathy, Autoimmune angioedema Bladder pain syndrome (also known brachial plexitis, and Parsonage- Autoimmune aplastic anemia (also as interstitial cystitis) Turner syndrome) known as aplastic anemia) Brachial neuritis (also known as Acute disseminated Autoimmune cardiomyopathy brachial plexus neuropathy, brachial encephalomyelitis (ADEM) Autoimmune dysautonomia plexitis, Parsonage-Turner syndrome, Acute necrotizing hemorrhagic acute brachial neuropathy, acute Autoimmune hemolytic anemia leukoencephalitis brachial radiculitis, and neuralgic Acute parapsoriasis (also known as Autoimmune hepatitis amyotrophy) acute guttate parapsoriasis, acute Autoimmune hyperlipidemia Bullous pemphigoid pityriasis lichenoides, parapsoriasis Autoimmune immunodeficiency Castleman’s disease (also varioliformis, Mucha-Habermann C known as giant lymph node disease, and parapsoriasis or Autoimmune inner ear disease hyperplasia, lymphoid hamartoma, pityriasis lichenoides et varioliformis (AIED) and angiofollicular lymph node acuta) Autoimmune myocarditis -
Development of Algorithms for Diagnosing Forms of Lichen Planus and Predicting of the Disease's Course
Development of algorithms for diagnosing forms of lichen planus and predicting of the disease’s course O.V. Serikova1, V.N. Kalaev2, N.A. Soboleva1 1Voronezh State Medical University, Studencheskaya, 10, 394000, Voronezh, Russia 2Voronezh State University, Universitetskaya PL. 1, 394000, Voronezh, Russia Abstract The work is devoted to application of mathematical methods and development of algorithms for diagnostics of the lichen planus forms that located at mucous membrane of the mouth and lips, the differential diagnosis of severe forms of other diseases and its prediction in difficult cases through the use of expert knowledge base, the results of the selection of the most informative features and micronucleus test’s interpretation in buccal epithelium. Keywords: lichen planus; differential diagnosis; Kohonen neural network 1. Introduction Diagnosis of lichen planus that located at the oral mucosa and the vermilion border has a significant interest among dentists, dermatologists, oncologists and doctors of other specialties. This is due to the lack of clear mechanisms of the disease development, severe, often permanent period, the existing trend towards malignancy elements of destruction, as well as frequent interaction with the General condition of the patient. Treatment of patients applying for dental care with pathology of the oral mucosa and lips, is one of the most challenging problems in dentistry because of the difficulties that occur by diagnosis of diseases in this body’s region. For example, the survey of 214 dentists, students of the improvement series in the Stomatology Department of the supplementary professional education Institute, Voronezh state medical University named after N. N. Burdenko, showed that only 30% of them are trying to make a diagnosis and prescribe treatment in cases of pathology of the oral mucosa and lips, and the remaining 70% of physicians send patients to the relevant medical Department of the University. -
Commission Implementing Decision (Eu) 2018
6.7.2018 EN Official Journal of the European Union L 170/1 II (Non-legislative acts) DECISIONS COMMISSION IMPLEMENTING DECISION (EU) 2018/945 of 22 June 2018 on the communicable diseases and related special health issues to be covered by epidemiological surveillance as well as relevant case definitions (Text with EEA relevance) THE EUROPEAN COMMISSION, Having regard to the Treaty on the Functioning of the European Union, Having regard to Decision No 1082/2013/EU of the European Parliament and of the Council of 22 October 2013 on serious cross-border threats to health and repealing Decision No 2119/98/EC (1), and in particular Article 6(5)(a) and (b) thereof, Whereas: (1) Pursuant to Decision No 2119/98/EC of the European Parliament and of the Council (2), Commission Decision 2000/96/EC (3) established a list of communicable diseases and special health issues to be covered by epidemiological surveillance in the Community network. (2) Commission Decision 2002/253/EC (4) laid down case definitions for reporting communicable diseases listed in Decision 2000/96/EC to the Community network. (3) The Annex to Decision No 1082/2013/EU sets out the criteria for selecting the communicable diseases and related special health issues to be covered by epidemiological surveillance within the network. (4) The list of diseases and related special health issues established by Decision 2000/96/EC should be updated to reflect changes in disease incidence and prevalence, the needs of the European Union and its Member States, as well as to ensure compliance with the criteria provided in the Annex to Decision No 1082/2013/EU. -
The Prevalence of Oral Lesions Among Palestinian Dental Patients Attending Oral Medicine Dental Clinics at Al-Quds University
Open Journal of Stomatology, 2020, 10, 300-309 https://www.scirp.org/journal/ojst ISSN Online: 2160-8717 ISSN Print: 2160-8709 The Prevalence of Oral Lesions among Palestinian Dental Patients Attending Oral Medicine Dental Clinics at Al-Quds University F. S. Habash, A. Ismail, R. O. Abu Hantash, M. Abu Younis Faculty of Dentistry, Al-Quds University, Jerusalem, Palestine How to cite this paper: Habash, F.S., Abstract Ismail, A., Abu Hantash, R.O. and Abu Younis, M. (2020) The Prevalence of Oral Objectives: In Palestine, there are no data about the prevalence of oral lesions Lesions among Palestinian Dental Patients or their associated risk factors. Thus, this study came to assess the prevalence Attending Oral Medicine Dental Clinics at and the risk factors of oral lesions among adult dental patients visiting Al- Al-Quds University. Open Journal of Sto- matology, 10, 300-309. Quds University (AQU) Dental Clinics. Materials and Methods: Three hun- https://doi.org/10.4236/ojst.2020.1010028 dred Twenty patients were diagnosed clinically for the presence of oral lesions at oral medicine clinics at Al-Quds University in the period between 2015 to Received: May 15, 2020 2016. Their age ranged from 21 to 60 years old (mean age: 40.2 ± 17.6). Se- Accepted: October 23, 2020 Published: October 26, 2020 nior students were trained to conduct the oral exam under the direct supervi- sion of Oral Medicine specialist. Trained students also collected data on pa- Copyright © 2020 by author(s) and tients’ demographics, dental history, medical history and other health related Scientific Research Publishing Inc.