Medical Terminology Course
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Inflammation 14.11. 2004
Inflammation • Inflammation is the response of living tissue to damage. The acute inflammatory response has 3 main functions. Inflammation • The affected area is occupied by a transient material called the acute inflammatory exudate . The exudate carries proteins, fluid and cells from local blood vessels into the damaged area to mediate local defenses. • If an infective causitive agent (e.g. bacteria) is present in the damaged area, it can be destroyed and eliminated by components of the exudate . 14.11. 2004 • The damaged tissue can be broken down and partialy liquefied, and the debris removed from the site of damage. Etiology Inflammation • The cause of acute inflammation may • In all these situations, the inflammatory be due to physical damage, chemical stimulus will be met by a series of changes in substances, micro-organisms or other the human body; it will induce production of agents. The inflammatory response certain cytokines and hormones which in turn consist of changes in blood flow, will regulate haematopoiesis, protein increased permeability of blood vessels and escape of cells from the synthesis and metabolism. blood into the tissues. The changes • Most inflammatory stimuli are controlled by a are essentially the same whatever the normal immune system. The human immune cause and wherever the site. system is divided into two parts which • Acute inflammation is short-lasting, constantly and closely collaborate - the innate lasting only a few days. and the adaptive immune system. Inflammation Syst emic manifesta tion • The innate system reacts promptly without specificity and memory. Phagocytic cells are important contributors in innate of inflammation reactivity together with enzymes, complement activation and acute phase proteins. -
The Ageing Haematopoietic Stem Cell Compartment
REVIEWS The ageing haematopoietic stem cell compartment Hartmut Geiger1,2, Gerald de Haan3 and M. Carolina Florian1 Abstract | Stem cell ageing underlies the ageing of tissues, especially those with a high cellular turnover. There is growing evidence that the ageing of the immune system is initiated at the very top of the haematopoietic hierarchy and that the ageing of haematopoietic stem cells (HSCs) directly contributes to changes in the immune system, referred to as immunosenescence. In this Review, we summarize the phenotypes of ageing HSCs and discuss how the cell-intrinsic and cell-extrinsic mechanisms of HSC ageing might promote immunosenescence. Stem cell ageing has long been considered to be irreversible. However, recent findings indicate that several molecular pathways could be targeted to rejuvenate HSCs and thus to reverse some aspects of immunosenescence. HSC niche The current demographic shift towards an ageing popu- The innate immune system is also affected by ageing. A specialized lation is an unprecedented global phenomenon that has Although an increase in the number of myeloid precur- microenvironment that profound implications. Ageing is associated with tissue sors has been described in the bone marrow of elderly interacts with haematopoietic attrition and an increased incidence of many types of can- people, the oxidative burst and the phagocytic capacity of stem cells (HSCs) to regulate cers, including both myeloid and lymphoid leukaemias, and both macrophages and neutrophils are decreased in these their fate. other haematopoietic cell malignancies1,2. Thus, we need individuals12,13. Moreover, the levels of soluble immune to understand the molecular and cellular mechanisms of mediators are altered with ageing. -
A Comparative Study of the Ultrastructure of Microvilli in the Epithelium of Small and Large Intestine of Mice
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by PubMed Central A COMPARATIVE STUDY OF THE ULTRASTRUCTURE OF MICROVILLI IN THE EPITHELIUM OF SMALL AND LARGE INTESTINE OF MICE T. M. MUKHERJEE and A. WYNN WILLIAMS From the Electron Microscope Laboratory, the Departlnent of Pathology, the University of Otago Medical School, Dunedin, New Zealand ABSTRACT A comparative analysis of the fine structure of the microvilli on jejunal and colonic epi- thelial cells of the mouse intestine has been made. The microvilli in these two locations demonstrate a remarkably similar fine structure with respect to the thickness of the plasma membrane, the extent of the filament-free zone, and the characteristics of the microfila- ments situated within the microvillous core. Some of the core microfilaments appear to continue across the plasma membrane limiting the tip of the microvillus. The main differ- ence between the microvilli of small intestine and colon is in the extent and organization of the surface coat. In the small intestine, in addition to the commonly observed thin surface "fuzz," occasional areas of the jejunal villus show a more conspicuous surface coat covering the tips of the microvilli. Evidence has been put forward which indicates that the surface coat is an integral part of the epithelial cells. In contrast to the jejunal epithelium, the colonic epithelium is endowed with a thicker surface coat. Variations in the organization of the surface coat at different levels of the colonic crypts have also been noted. The func- tional significance of these variations in the surface coat is discussed. -
WHITE BLOOD CELLS Formation Function ~ TEST YOURSELF
Chapter 9 Blood, Lymph, and Immunity 231 WHITE BLOOD CELLS All white blood cells develop in the bone marrow except Any nucleated cell normally found in blood is a white blood for some lymphocytes (they start out in bone marrow but cell. White blood cells are also known as WBCs or leukocytes. develop elsewhere). At the beginning of leukopoiesis all the When white blood cells accumulate in one place, they grossly immature white blood cells look alike even though they're appear white or cream-colored. For example, pus is an accu- already committed to a specific cell line. It's not until the mulation of white blood cells. Mature white blood cells are cells start developing some of their unique characteristics larger than mature red blood cells. that we can tell them apart. There are five types of white blood cells. They are neu- Function trophils, eosinophils, basophils, monocytes and lymphocytes (Table 9-2). The function of all white blood cells is to provide a defense White blood cells can be classified in three different ways: for the body against foreign invaders. Each type of white 1. Type of defense function blood cell has its own unique role in this defense. If all the • Phagocytosis: neutrophils, eosinophils, basophils, mono- white blood cells are functioning properly, an animal has a cytes good chance of remaining healthy. Individual white blood • Antibody production and cellular immunity: lympho- cell functions will be discussed with each cell type (see cytes Table 9-2). 2. Shape of nucleus In providing defense against foreign invaders, the white • Polymorphonuclear (multilobed, segmented nucleus): blood cells do their jobs primarily out in the tissues. -
Iliopsoas Tendonitis/Bursitis Exercises
ILIOPSOAS TENDONITIS / BURSITIS What is the Iliopsoas and Bursa? The iliopsoas is a muscle that runs from your lower back through the pelvis to attach to a small bump (the lesser trochanter) on the top portion of the thighbone near your groin. This muscle has the important job of helping to bend the hip—it helps you to lift your leg when going up and down stairs or to start getting out of a car. A fluid-filled sac (bursa) helps to protect and allow the tendon to glide during these movements. The iliopsoas tendon can become inflamed or overworked during repetitive activities. The tendon can also become irritated after hip replacement surgery. Signs and Symptoms Iliopsoas issues may feel like “a pulled groin muscle”. The main symptom is usually a catch during certain movements such as when trying to put on socks or rising from a seated position. You may find yourself leading with your other leg when going up the stairs to avoid lifting the painful leg. The pain may extend from the groin to the inside of the thigh area. Snapping or clicking within the front of the hip can also be experienced. Do not worry this is not your hip trying to pop out of socket but it is usually the iliopsoas tendon rubbing over the hip joint or pelvis. Treatment Conservative treatment in the form of stretching and strengthening usually helps with the majority of patients with iliopsoas bursitis. This issue is the result of soft tissue inflammation, therefore rest, ice, anti- inflammatory medications, physical therapy exercises, and/or injections are effective treatment options. -
Diverse T-Cell Differentiation Potentials of Human Fetal Thymus, Fetal Liver, Cord Blood and Adult Bone Marrow CD34 Cells On
IMMUNOLOGY ORIGINAL ARTICLE Diverse T-cell differentiation potentials of human fetal thymus, fetal liver, cord blood and adult bone marrow CD34 cells on lentiviral Delta-like-1-modified mouse stromal cells Ekta Patel,1 Bei Wang,1 Lily Lien,2 Summary Yichen Wang,2 Li-Jun Yang,3 Jan Human haematopoietic progenitor/stem cells (HPCs) differentiate into S. Moreb4 and Lung-Ji Chang1 functional T cells in the thymus through a series of checkpoints. A conve- 1Department of Molecular Genetics and nient in vitro system will greatly facilitate the understanding of T-cell Microbiology, College of Medicine, University of Florida, Gainesville, FL, USA, 2Vectorite development and future engineering of therapeutic T cells. In this report, Biomedica Inc., Taipei, Taiwan, 3Department we established a lentiviral vector-engineered stromal cell line (LSC) of Pathology, Immunology and Laboratory expressing the key lymphopoiesis regulator Notch ligand, Delta-like 1 Medicine, University of Florida, Gainesville, (DL1), as feeder cells (LSC-mDL1) supplemented with Flt3 ligand (fms- 4 FL, USA, and Department of Medicine, like tyrosine kinase 3, Flt3L or FL) and interleukin-7 for the development University of Florida, Gainesville, FL, USA of T cells from CD34+ HPCs. We demonstrated T-cell development from human HPCs with various origins including fetal thymus (FT), fetal liver (FL), cord blood (CB) and adult bone marrow (BM). The CD34+ HPCs from FT, FL and adult BM expanded more than 100-fold before reaching the b-selection and CD4/CD8 double-positive T-cell stage. The CB HPCs, on the other hand, expanded more than 1000-fold before b-selection. -
The Textual and Visual Uses of the Literary Motif of Cross-Dressing In
The Textual and Visual Uses of the Literary Motif of Cross-Dressing in Medieval French Literature, 1200–1500 Vanessa Elizabeth Wright Submitted in accordance with the requirements for the degree of PhD in Medieval Studies University of Leeds Institute for Medieval Studies September 2019 2 The candidate confirms that the work submitted is her own and that appropriate credit has been given where reference has been made to the work of others. This copy has been supplied on the understanding that it is copyright material and that no quotation from the thesis may be published without proper acknowledgement. The right of Vanessa Elizabeth Wright to be identified as Author of this work has been asserted by her in accordance with the Copyright, Designs and Patents Act 1988. 3 Acknowledgements I would like to thank my supervisors Rosalind Brown-Grant, Catherine Batt, and Melanie Brunner for their guidance, support, and for continually encouraging me to push my ideas further. They have been a wonderful team of supervisors and it has been a pleasure to work with them over the past four years. I would like to thank my examiners Emma Cayley and Helen Swift for their helpful comments and feedback on this thesis and for making my viva a positive and productive experience. I gratefully acknowledge the funding that allowed me to undertake this doctoral project. Without the School of History and the Institute for Medieval Studies Postgraduate Research Scholarship, I would not have been able to undertake this study. Trips to archives and academic conferences were made possible by additional bursaries and fellowships from Institute for Medieval Studies, the Royal Historical Society, the Society for the Study of Medieval Languages and Literatures, the Society for Medieval Feminist Scholarship’s Foremothers Fellowship (2018), and the Society for the Study of French History. -
Isaac Newton Academy Revision Booklet- Exam 1
Isaac Newton Academy Revision Booklet- Exam 1 Component 01: Physical factors affecting performance 1.1 Applied anatomy and physiology 1.2 Physical training. Functions of the skeleton Location of Major Bones Bone stores crucial nutrients, minerals, and lipids and produces blood cells that nourish the body and play a vital role in protecting the body against infection. Bones have many functions, including the following: Support: Bones provide a framework for the attachment of muscles and other tissues. Bone Location Arm - humerus, radius and ulna. Hand - Carpals, Metacarpals and Phalanges. Sternum and Ribs. Femur – the thigh bone. Patella – the knee cap. Tibia – the shin bone, the larger of the two leg bones located below the knee cap. Fibula – the smaller of the two leg bones located below the knee cap. The OCR Spec expects us to know the following regarding synovial joints: The definition of a synovial joint, Articulating bones of the knee and elbow hinge joints and also the articulating bones of the shoulder and hip Ball and socket joints Hinge Joint- A hinge joint is found at the knee and the elbow, Synovial Joint- This is a freely moveable joint in thich the bones’ surfaces are covered Articulating bones of the elbow by cartilage and connected by joint are the Humerus radius fibrous connective tissue and Ulna . Articulating bones of capsule lines with synovial the knee are the Femur and fluid Tibia. Ball and socket joint- Allows a wide range of movement, they can be Articulating bones- These found at the hip and shoulder. are bones that move within a joint Articulating bones of the shoulder are Humerus and Scapula. -
Medical Glossary
medical glossary AC Joint — Acromioclavicular joint; joint of the Bone Scan — An imaging procedure in which a Edema — Accumulation of fluid in organs and tis- shoulder where acromion process of the scapula radioactive-labeled substance is injected into the sues of the body (swelling). and the distal end of the clavicle meet; most shoul- body to determine the status of a bony injury. If the Effusion — Accumulation of fluid, in various der separations occur at this point. radioactive substance is taken up the bone at the spaces in the body, or the knee itself. Commonly, Abduct — Movement of any extremity away from injury site, the injury will show as a “hot spot” on the knee has an effusion after an injury. the midline of the body. This action is achieved by the scan image. The bone scan is particularly use- ful in the diagnosis of stress fractures. Electrical Galvanic Stimulation (EGS) — An elec- an abductor muscle. trical therapeutic modality that sends a current to Abrasion — Any injury which rubs off the surface Brachial Plexus — Network of nerves originating the body at select voltages and frequencies in of the skin. from the cervical vertebrae and running down to order to stimulate pain receptors, disperse edema, the shoulder, arm, hand, and fingers. Abscess — An infection which produces pus; can or neutralize muscle spasms among other function- be the result of a blister, callus, penetrating wound Bruise — A discoloration of the skin due to an al applications. or laceration. extravasation of blood into the underlying tissues. Electromyogran (EMG) — Test to determine nerve Adduct — Movement of an extremity toward the Bursa — A fluid-filled sac that is located in areas function. -
Dignity on Trial RIGHTS India’S Need for Sound Standards for Conducting and Interpreting Forensic Examinations of Rape Survivors WATCH
India HUMAN Dignity on Trial RIGHTS India’s Need for Sound Standards for Conducting and Interpreting Forensic Examinations of Rape Survivors WATCH Dignity on Trial India’s Need for Sound Standards for Conducting and Interpreting Forensic Examinations of Rape Survivors Copyright © 2010 Human Rights Watch All rights reserved. Printed in the United States of America ISBN: 1-56432-681-0 Cover design by Rafael Jimenez Human Rights Watch 350 Fifth Avenue, 34th floor New York, NY 10118-3299 USA Tel: +1 212 290 4700, Fax: +1 212 736 1300 [email protected] Poststraße 4-5 10178 Berlin, Germany Tel: +49 30 2593 06-10, Fax: +49 30 2593 0629 [email protected] Avenue des Gaulois, 7 1040 Brussels, Belgium Tel: + 32 (2) 732 2009, Fax: + 32 (2) 732 0471 [email protected] 64-66 Rue de Lausanne 1202 Geneva, Switzerland Tel: +41 22 738 0481, Fax: +41 22 738 1791 [email protected] 2-12 Pentonville Road, 2nd Floor London N1 9HF, UK Tel: +44 20 7713 1995, Fax: +44 20 7713 1800 [email protected] 27 Rue de Lisbonne 75008 Paris, France Tel: +33 (1)43 59 55 35, Fax: +33 (1) 43 59 55 22 [email protected] 1630 Connecticut Avenue, N.W., Suite 500 Washington, DC 20009 USA Tel: +1 202 612 4321, Fax: +1 202 612 4333 [email protected] Web Site Address: http://www.hrw.org September 2010 1-56432-681-0 Dignity on Trial India’s Need for Sound Standards for Conducting and Interpreting Forensic Examinations of Rape Survivors I. Summary and Recommendations ..................................................................................... 1 The Finger Test .............................................................................................................. -
Side-Branching in the Mammary Gland: the Progesterone–Wnt Connection
Downloaded from genesdev.cshlp.org on September 27, 2021 - Published by Cold Spring Harbor Laboratory Press PERSPECTIVE Side-branching in the mammary gland: the progesterone–Wnt connection Gertraud W. Robinson,1 Lothar Hennighausen, and Peter F. Johnson2 Laboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0822 USA; 2Eukaryotic Transcriptional Regulation Section, Regulation of Cell Growth Laboratory, National Cancer Institute-Frederick Cancer Research Development Center (FCRDC), Frederick, Maryland 21702-1201 USA The mammary gland is a derivative of the ectoderm mammary ducts during puberty and pregnancy. Their whose development begins in the embryo and progresses studies demonstrate that a nuclear signal is converted after birth. The major part of development occurs in the into a secreted signal that can control the fate of adjacent adolescent and adult animal. Hormones produced by the cells in a paracrine fashion. A genetic understanding of pituitary, the ovaries, the uterus, the placenta, and the this and other signaling pathways regulating cell growth mammary gland itself control this process. Over the past in the mammary gland will improve our ability to ma- century, surgical, biological, and genetic tools have been nipulate these processes and thus design strategies for used to gain insight into physiological and pathological prevention and treatment of breast cancer. processes in the mammary gland. Originally, endocrine ablation and reconstitution experiments provided a de- scriptive framework of the role of ovarian and pituitary Tools to investigate signaling pathways hormones (Halban 1900; Nandi 1958). These experi- Several features of the mammary gland provide unique ments demonstrated a clear requirement for the ovarian opportunities for experimental manipulations to inte- steroids estrogen and progesterone for ductal growth and grate systemic, local and cell-specific signaling path- alveolar development (Topper and Freeman 1980). -
Study Guide Medical Terminology by Thea Liza Batan About the Author
Study Guide Medical Terminology By Thea Liza Batan About the Author Thea Liza Batan earned a Master of Science in Nursing Administration in 2007 from Xavier University in Cincinnati, Ohio. She has worked as a staff nurse, nurse instructor, and level department head. She currently works as a simulation coordinator and a free- lance writer specializing in nursing and healthcare. All terms mentioned in this text that are known to be trademarks or service marks have been appropriately capitalized. Use of a term in this text shouldn’t be regarded as affecting the validity of any trademark or service mark. Copyright © 2017 by Penn Foster, Inc. All rights reserved. No part of the material protected by this copyright may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without permission in writing from the copyright owner. Requests for permission to make copies of any part of the work should be mailed to Copyright Permissions, Penn Foster, 925 Oak Street, Scranton, Pennsylvania 18515. Printed in the United States of America CONTENTS INSTRUCTIONS 1 READING ASSIGNMENTS 3 LESSON 1: THE FUNDAMENTALS OF MEDICAL TERMINOLOGY 5 LESSON 2: DIAGNOSIS, INTERVENTION, AND HUMAN BODY TERMS 28 LESSON 3: MUSCULOSKELETAL, CIRCULATORY, AND RESPIRATORY SYSTEM TERMS 44 LESSON 4: DIGESTIVE, URINARY, AND REPRODUCTIVE SYSTEM TERMS 69 LESSON 5: INTEGUMENTARY, NERVOUS, AND ENDOCRINE S YSTEM TERMS 96 SELF-CHECK ANSWERS 134 © PENN FOSTER, INC. 2017 MEDICAL TERMINOLOGY PAGE III Contents INSTRUCTIONS INTRODUCTION Welcome to your course on medical terminology. You’re taking this course because you’re most likely interested in pursuing a health and science career, which entails proficiencyincommunicatingwithhealthcareprofessionalssuchasphysicians,nurses, or dentists.