Confusing Presentations of Hodgkin Lymphoma
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Follicular Lymphoma
Follicular Lymphoma What is follicular lymphoma? Let us explain it to you. www.anticancerfund.org www.esmo.org ESMO/ACF Patient Guide Series based on the ESMO Clinical Practice Guidelines FOLLICULAR LYMPHOMA: A GUIDE FOR PATIENTS PATIENT INFORMATION BASED ON ESMO CLINICAL PRACTICE GUIDELINES This guide for patients has been prepared by the Anticancer Fund as a service to patients, to help patients and their relatives better understand the nature of follicular lymphoma and appreciate the best treatment choices available according to the subtype of follicular lymphoma. We recommend that patients ask their doctors about what tests or types of treatments are needed for their type and stage of disease. The medical information described in this document is based on the clinical practice guidelines of the European Society for Medical Oncology (ESMO) for the management of newly diagnosed and relapsed follicular lymphoma. This guide for patients has been produced in collaboration with ESMO and is disseminated with the permission of ESMO. It has been written by a medical doctor and reviewed by two oncologists from ESMO including the lead author of the clinical practice guidelines for professionals, as well as two oncology nurses from the European Oncology Nursing Society (EONS). It has also been reviewed by patient representatives from ESMO’s Cancer Patient Working Group. More information about the Anticancer Fund: www.anticancerfund.org More information about the European Society for Medical Oncology: www.esmo.org For words marked with an asterisk, a definition is provided at the end of the document. Follicular Lymphoma: a guide for patients - Information based on ESMO Clinical Practice Guidelines – v.2014.1 Page 1 This document is provided by the Anticancer Fund with the permission of ESMO. -
Circle) None Fever Night Sweats Wt Loss Laboratory Studies Hgb WBC Plate
LYMPHOMA STAGING DIAGRAM Instructions: boxed items must be completed History B Sx (Circle) none fever night sweats wt loss Laboratory studies Hgb WBC Plate ECOG performance status g/L x109/L x109/L LDH (patient/upper normal) / CERVICAL PRE-AURICULAR HIV antibody pos neg WALDEYER'S RING UPPER CERVICAL MEDIAN OR LOWER CERVICAL HBsAg pos neg POSTERIOR CERVICAL SUPRACLAVICULAR INFRACLAVICULAR MEDIASTINAL HBcoreAb pos neg PARATRACHEAL MEDIASTINAL AXILLARY Hep C Ab pos neg AXILLARY HILAR RETROCRURAL SPE monoclonal protein pos neg type____________ SPLEEN PARA AORTIC PARA AORTIC MESENTERIC For Hodgkin lymphoma only CELIAC COMMON ILIAC SPLENIC (HEPATIC) HILAR EXTERNAL ILIAC PORTAL Albumin g/L INGUINAL MESENTERIC Lymphs x 109/L INGUINAL FEMORAL OTHER EPITROCHLEAR POPLITEAL Treatment Largest tumor diameter (nearest whole cm) Treatment plan Initial biopsy site Date (d/m/y) / / Histologic diagnosis Doctor in Charge 1 _________________________________________ 2 Reason for referral Bone marrow pos neg not done New Recurrent Follow-up Completed by _______________ Date____________ List all other extranodal sites here 1 2 Complete if diagnosis or stage subsequently changed 3 4 Diagnosis/Stage amended to _________________________ 5 Reason__________________________________________ 6 By_______________________ Date______________ Stage (circle) 0 1 2 3 4 A B E This staging diagram can be found on NOTIFY PATIENT INFORMATION IF STAGE OR H:lym_docs\staging\lymphoma.doc DIAGNOSIS IS AMENDED Form #TH-41 Revised 26 March 2007 LYMPHOMA AND CHRONIC LYMPHOCYTIC LEUKEMIA STAGING SYSTEMS BCCA LYMPHOMA, HODGKIN AND CHRONIC LYMPHOCYTIC LEUKEMIA NON-HODGKIN 1982 STAGE FINDINGS STAGE INVOLVEMENT 0 Lymphocyte count > 5.0 x 109 /L 1 Single lymph node region (1) or one Bone marrow contains 40% extralymphatic site (1E). -
Extra-Intestinal Manifestations of Inflammatory Bowel Disease
Open Access Review Article DOI: 10.7759/cureus.17187 Extra-Intestinal Manifestations of Inflammatory Bowel Disease Aliya H. Sange 1 , Natasha Srinivas 2 , Mubashira K. Sarnaik 3 , Srimy Modi 1 , Yasaswi Pisipati 4 , Sarayoo Vaidya 3 , Naqvi Syed Gaggatur 3 , Ibrahim Sange 5, 6 1. Research, K.J. Somaiya Medical College, Mumbai, IND 2. Research, BGS Global Institute of Medical Sciences, Bangalore, IND 3. Internal Medicine, M.S. Ramaiah Medical College, Bangalore, IND 4. Psychiatry, M.S. Ramaiah Medical College, Bangalore, IND 5. Research, California Institute of Behavioral Neurosciences & Psychology, Fairfield, USA 6. Medicine, K.J. Somaiya Medical College, Mumbai, IND Corresponding author: Aliya H. Sange, [email protected] Abstract Inflammatory bowel disease (IBD) is associated with extra-intestinal manifestations (EIMs) that tend to parallel intestinal activity and have a debilitating effect on the quality of life. EIMs primarily affect the joints, skin, and eyes with less frequent involvement of the liver, kidney, and pancreas. This article reviews the prevalence of musculoskeletal, dermatological, ocular, and other manifestations in IBD and their coalition with underlying intestinal inflammation. EIMs occurring independently of intestinal activity are managed by targeted therapies, categorical regimens, and specific treatments. On the other hand, EIMs paralleling the bowel activity are carefully monitored while the IBD is brought under control. Since the etiology of the disease is responsible for the development of the EIMs, the research scrutinizes the identified pathogenic mechanisms that tend to involve genetic susceptibility, aberrant self-recognition, and autoantibodies directed against organ-specific antigens shared by intestinal and extra-intestinal organs. This article also provides an overview of the epidemiology, clinical features, diagnostic modalities, and management of the EIMs associated with IBD. -
History Lectured on Midwifery at St Bartholomew’S Hospital and and Was in Attendance at the Births of All of Her Children
J R Coll Physicians Edinb 2012; 42:274–9 Paper http://dx.doi.org/10.4997/JRCPE.2012.317 © 2012 Royal College of Physicians of Edinburgh Sir Charles Locock and potassium bromide MJ Eadie Honorary Research Consultant and Emeritus Professor, Faculty of Health Sciences, University of Queensland, Royal Brisbane and Women’s Hospital, Australia ABSTRACT On 12 May 1857, Edward Sieveking read a paper on epilepsy to the Correspondence to M Eadie Royal Medical and Chirurgical Society in London. During the discussion that Faculty of Health Sciences, followed Sir Charles Locock, obstetrician to Queen Victoria, was reported to have University of Queensland, Royal Brisbane and Women’s commented that during the past 14 months he had used potassium bromide to Hospital, Herston, successfully stop epileptic seizures in all but one of 14 or 15 women with ‘hysterical’ Brisbane 4029, Australia or catamenial epilepsy. This report of Locock’s comment has generally given him credit for introducing the first reasonably effective antiepileptic drug into medical Tel 61 2 (0)7 38311704 e-mail [email protected] practice. However examination of the original reports raises questions as to how soundly based the accounts of Locock’s comments were. Subsequently, others using the drug to treat epilepsy failed to obtain the degree of benefit that the reports of Locock’s comments would have led them to expect. The drug might not have come into more widespread use as a result, had not Samuel Wilks provided good, independent evidence for the drug’s antiepileptic efficacy in 1861. KEYWORDS Epilepsy treatment, Charles Locock, potassium bromide, Edward Sieveking, Samuel Wilks DECLaratIONS OF INTERESTS No conflicts of interest declared. -
Editorial Ulcerative Colitis: the Scope of the Scopes in Nomenclature and Diagnosis
Tropical Gastroenterology 2011;32(2):87–93 Editorial Ulcerative Colitis: The scope of the scopes in nomenclature and diagnosis S. Datta Gupta Department of Pathology Life-long learning is the hall-mark of professional education. This is often the result of All India Institute of Medical Sciences experiences shared by our colleagues world-wide, of common clinical conditions that present New Delhi - 110029, India in an unusual manner. Correspondence: The two major constituents of inflammatory bowel disease: Crohn’s disease (CD) and Dr. S. Datta Gupta ulcerative colitis (UC) have several overlapping features and their distinction in difficult Email: [email protected] cases is a true accreditation of the skills of a gastroenterologist. Indistinguishable cases are aptly labeled as indeterminate colitis. In certain countries such as India, additionally, colonic tuberculosis (TB) is a close differential of colonic Crohn’s disease mainly because both are recognized to show patchy involvement and granulomatous inflammation. In this issue of the journal, Shah SN, Amarapurkar AD, Thiruvengadam NR, Nistala S and Rathi PM1 highlight unusual presentations of ulcerative colitis that may make the diagnosis otherwise difficult. Non-contagious diarrheal diseases have been apparent to physicians over centuries having been described by Aretaeus (A.D. 300) and Soranus (A.D. 117).2 Sir Samuel Wilks in 18593 has been credited with introducing the term “ulcerative colitis” to a disease that was less understood then and perhaps even lesser understood today. It is likely that several clinically similar diseases may have been considered under this term. Thus it has been suggested that in 1745 Prince Charles, the Young Pretender to the throne, cured himself of ulcerative colitis by adopting a milk-free diet!2,4 Excellent descriptions have been provided by the Surgeon General of the Union Army (describing the medical history of the American Civil War), Wilks & Moxon (1875), Allchin (1885) and Hale-White (1888). -
The Lymphoma Guide Information for Patients and Caregivers
The Lymphoma Guide Information for Patients and Caregivers Ashton, lymphoma survivor This publication was supported by Revised 2016 Publication Update The Lymphoma Guide: Information for Patients and Caregivers The Leukemia & Lymphoma Society wants you to have the most up-to-date information about blood cancer treatment. See below for important new information that was not available at the time this publication was printed. In November 2017, the Food and Drug Administration (FDA) approved obinutuzumab (Gazyva®) in combination with chemotherapy, followed by Gazyva alone in those who responded, for people with previously untreated advanced follicular lymphoma (stage II bulky, III or IV). In November 2017, the Food and Drug Administration (FDA) approved brentuximab vedotin (Adcetris®) for treatment of adult patients with primary cutaneous anaplastic large cell lymphoma (pcALCL) or CD30- expressing mycosis fungoides (MF) who have received prior systemic therapy. In October 2017, the Food and Drug Administration (FDA) approved acalabrutinib (CalquenceTM) for the treatment of adults with mantle cell lymphoma who have received at least one prior therapy. In October 2017, the Food and Drug Administration (FDA) approved axicabtagene ciloleucel (Yescarta™) for the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, primary mediastinal large B-cell lymphoma, high-grade B-cell lymphoma, and DLBCL arising from follicular lymphoma. Yescarta is a CD19-directed genetically modified autologous T cell immunotherapy FDA approved. Yescarta is not indicated for the treatment of patients with primary central nervous system lymphoma. In September 2017, the Food and Drug Administration (FDA) approved copanlisib (AliqopaTM) for the treatment of adult patients with relapsed follicular lymphoma (FL) who have received at least two prior systemic therapies. -
Anaplastic Large Cell Lymphoma (ALCL)
Helpline (freephone) 0808 808 5555 [email protected] www.lymphoma-action.org.uk Anaplastic large cell lymphoma (ALCL) This page is about anaplastic large-cell lymphoma (ALCL), a type of T-cell lymphoma. On this page What is ALCL? Who gets it? Symptoms Treatment Relapsed and refractory ALCL Research and targeted treatments We have separate information about the topics in bold font. Please get in touch if you’d like to request copies or if you would like further information about any aspect of lymphoma. Phone 0808 808 5555 or email [email protected]. What is ALCL? Anaplastic large cell lymphoma (ALCL) is a type of T-cell lymphoma – a non-Hodgkin lymphoma that develops from white blood cells called T cells. Under a microscope, the cancerous cells in ALCL look large, undeveloped and very abnormal (‘anaplastic’). There are four main types of ALCL. They have complicated names based on their features and the types of proteins they make: • ALK-positive ALCL (also known as ALK+ ALCL) is the most common type. In ALK-positive ALCL, the abnormal T cells have a genetic change (mutation) that means they make a protein called ‘anaplastic lymphoma kinase’ (ALK). In other words, they test positive for ALK. ALK-positive ALCL is a fast-growing (high-grade) lymphoma. Page 1 of 6 © Lymphoma Action • ALK-negative ALCL (also known as ALK- ALCL) is a high-grade lymphoma that accounts for around 3 in every 10 cases of ALCL. The abnormal T cells do not make the ALK protein – they test negative for ALK. -
Slater V. Baker and Stapleton (C.B. 1767): Unpublished Monographs by Robert D. Miller
SLATER V. BAKER AND STAPLETON (C.B. 1767): UNPUBLISHED MONOGRAPHS BY ROBERT D. MILLER ROBERT D. MILLER, J.D., M.S. HYG. HONORARY FELLOW MEDICAL HISTORY AND BIOETHICS DEPARTMENT SCHOOL OF MEDICINE AND PUBLIC HEALTH UNIVERSITY OF WISCONSIN - MADISON PRINTED BY AUTHOR MADISON, WISCONSIN 2019 © ROBERT DESLE MILLER 2019 BOUND BY GRIMM BOOK BINDERY, MONONA, WI AUTHOR’S INTRODUCTION These unpublished monographs are being deposited in several libraries. They have their roots in my experience as a law student. I have been interested in the case of Slater v. Baker and Stapleton since I first learned of it in law school. I was privileged to be a member of the Yale School Class of 1974. I took an elective course with Dr. Jay Katz on the protection of human subjects and then served as a research assistant to Dr. Katz in the summers of 1973 and 1974. Dr. Katz’s course used his new book EXPERIMENTATION WITH HUMAN BEINGS (New York: Russell Sage Foundation 1972). On pages 526-527, there are excerpts from Slater v. Baker. I sought out and read Slater v. Baker. It seemed that there must be an interesting backstory to the case, but it was not accessible at that time. I then practiced health law for nearly forty years, representing hospitals and doctors, and writing six editions of a textbook on hospital law. I applied my interest in experimentation with human beings by serving on various Institutional Review Boards (IRBs) during that period. IRBs are federally required committees that review and approve experiments with humans at hospitals, universities and other institutions. -
CD20-Negative Diffuse Large B-Cell Lymphomas: Biology and Emerging Therapeutic Options
Expert Review of Hematology ISSN: 1747-4086 (Print) 1747-4094 (Online) Journal homepage: http://www.tandfonline.com/loi/ierr20 CD20-negative diffuse large B-cell lymphomas: biology and emerging therapeutic options Jorge J Castillo, Julio C Chavez, Francisco J Hernandez-Ilizaliturri & Santiago Montes-Moreno To cite this article: Jorge J Castillo, Julio C Chavez, Francisco J Hernandez-Ilizaliturri & Santiago Montes-Moreno (2015) CD20-negative diffuse large B-cell lymphomas: biology and emerging therapeutic options, Expert Review of Hematology, 8:3, 343-354, DOI: 10.1586/17474086.2015.1007862 To link to this article: http://dx.doi.org/10.1586/17474086.2015.1007862 Published online: 01 Feb 2015. Submit your article to this journal Article views: 165 View related articles View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=ierr20 Download by: [North Shore Med Ctr], [Jorge Castillo] Date: 16 March 2016, At: 07:44 Review CD20-negative diffuse large B-cell lymphomas: biology and emerging therapeutic options Expert Rev. Hematol. 8(3), 343–354 (2015) Jorge J Castillo*1, CD20-negative diffuse large B-cell lymphoma (DLBCL) is a rare and heterogeneous group of Julio C Chavez2, lymphoproliferative disorders. Known variants of CD20-negative DLBCL include plasmablastic Francisco J lymphoma, primary effusion lymphoma, large B-cell lymphoma arising in human herpesvirus 8-associated multicentric Castleman disease and anaplastic lymphoma kinase-positive DLBCL. Hernandez-Ilizaliturri3 Given the lack of CD20 expression, atypical cellular morphology and aggressive clinical and Santiago 4 behavior characterized by chemotherapy resistance and inferior survival rates, CD20-negative Montes-Moreno DLBCL represents a challenge from the diagnostic and therapeutic perspectives. -
The Contribution of T Cell-Derived Cytokines and Proteases to Chronic Inflammation in the Human Intestine
The contribution of T cell-derived cytokines and proteases to chronic inflammation in the human intestine by Paolo Biancheri A thesis submitted for the Degree of Doctor of Philosophy Supervisor: Prof Thomas T MacDonald Second supervisor: Prof Andrew Silver Queen Mary University of London Barts and The London School of Medicine and Dentistry London - United Kingdom 2016 This work is dedicated to the memory of my grandparents Margherita, Luigi, Bianca, and Paolo 2 Statement of originality I, Paolo Biancheri, confirm that the research included within this thesis is my own work or that, where it has been carried out in collaboration with, or supported by others, this is duly acknowledged below and my contribution indicated. Previously published material is also acknowledged below. I attest that I have exercised reasonable care to ensure that the work is original, and does not to the best of my knowledge break any UK law, infringe any third party’s copyright or other Intellectual Property Right, or contain any confidential material. I accept that the College has the right to use plagiarism detection software to check the electronic version of the thesis. I confirm that this thesis has not been previously submitted for the award of a degree by this or any other university. The copyright of this thesis rests with the author and no quotation from it or information derived from it may be published without the prior written consent of the author. Signature: Date: 28.02.2016 Details of collaboration I declare that the work presented in this thesis is my own, with the exception of some of the experiments reported in Chapters 3, 4 and 6, which, upon obtaining approval from the owners of the data, have been included in this thesis and have been listed in the Note at the beginning of the Chapters. -
Non-Hodgkin Lymphoma
Non-Hodgkin Lymphoma Rick, non-Hodgkin lymphoma survivor This publication was supported in part by grants from Revised 2013 A Message From John Walter President and CEO of The Leukemia & Lymphoma Society The Leukemia & Lymphoma Society (LLS) believes we are living at an extraordinary moment. LLS is committed to bringing you the most up-to-date blood cancer information. We know how important it is for you to have an accurate understanding of your diagnosis, treatment and support options. An important part of our mission is bringing you the latest information about advances in treatment for non-Hodgkin lymphoma, so you can work with your healthcare team to determine the best options for the best outcomes. Our vision is that one day the great majority of people who have been diagnosed with non-Hodgkin lymphoma will be cured or will be able to manage their disease with a good quality of life. We hope that the information in this publication will help you along your journey. LLS is the world’s largest voluntary health organization dedicated to funding blood cancer research, education and patient services. Since 1954, LLS has been a driving force behind almost every treatment breakthrough for patients with blood cancers, and we have awarded almost $1 billion to fund blood cancer research. Our commitment to pioneering science has contributed to an unprecedented rise in survival rates for people with many different blood cancers. Until there is a cure, LLS will continue to invest in research, patient support programs and services that improve the quality of life for patients and families. -
Samuel Simms Medical Collection
Shelfmark Title Author Publication Information Clinical lectures on diseases of the nervous system, delivered at the Infirmary of La Salpêtrière / by Charcot, J. M. (Jean London : New Sydenham Society, Simm/ RC358 CHAR Professor J.M. Charcot ; translated by Thomas Sv ill ; containing eighty-six woodcuts. Martin) 1889. Simm/ p QP101 FAUR Ars medica Italorum laus : la scoperta della circolazione del sangue è gloria italiana. Faure, Giovanni. Roma : Don Luigi Guanella" 1933 Brockbank, Edward Manchester (Eng.) : G. Falkner, Simm/ p QD22.D2 BROC John Dalton, experimental physiologist and would-be physician / by E. M. Brockbank. Mansfield, 1866- 1929. Queen's University of q Z988 QUEE Interim short-title list of Samuel Simms collection (in the Medical Library). Belfast. Library. Belfast : 1965-1972. Sepulchretum, sive, Anatomia practica : ex cadaveribus morbo denatis, proponens historias et observationes omnium humani corporis affectuum, ipsorumq : causas reconditas revelans : quo nomine, tam pathologiæ genuinæ, quà m nosocomiæ orthodoxæ fundatrix, imo medicinæ veteris Bonet, Théophile, Genevæ : Sumptibus Cramer & Simm/ f RB24 BONE ac novæ promptuarium, dici meretur : cum indicibus necessariis / Theophili Boneti. 1620-1689. Perachon, 1700. Jo. Baptistæ Morgagni P. P. P. P. De sedibus, et causis morborum per anatomen indagatis libri quinque : Dissectiones, et animadversiones, nunc primum editas, complectuntur propemodum innumeras, medicis, chirurgis, anatomicis profuturas. Multiplex præfixus est index rerum, & nominum Morgagni, Giambattista, Venetiis : Ex typographia Simm/ f RB24 MORG accuratissimus. Tomus primus (-secundus). 1682-1771. Remondiniana, MDCCLXI (1761). Ortus medicinae, id est Initia physicae inaudita : progressus medicinae nouus, in morborum vltionem Lugduni : Sumptibus Ioan. Ant. ad vitam longam / authore Ioan. Baptista Van Helmont ... ; edente authoris filio Francisco Mercurio Van Helmont, Jean Baptiste Huguetan, & Guillielmi Barbier, Simm/ f R128.7 HELM Helmont ; cum eius praefatione ex Belgico translata.