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Digitalcommons@UNMC Agranulocytosis
University of Nebraska Medical Center DigitalCommons@UNMC MD Theses Special Collections 5-1-1935 Agranulocytosis Gordon A. Gunn University of Nebraska Medical Center This manuscript is historical in nature and may not reflect current medical research and practice. Search PubMed for current research. Follow this and additional works at: https://digitalcommons.unmc.edu/mdtheses Part of the Medical Education Commons Recommended Citation Gunn, Gordon A., "Agranulocytosis" (1935). MD Theses. 386. https://digitalcommons.unmc.edu/mdtheses/386 This Thesis is brought to you for free and open access by the Special Collections at DigitalCommons@UNMC. It has been accepted for inclusion in MD Theses by an authorized administrator of DigitalCommons@UNMC. For more information, please contact [email protected]. AGRANULOOYTOSIS ,- Senior Thesis by GOrdon .M.. Gunn INTRODUCTION Fifteen years ago the medioal profession new nothing of the disease spoken of in this paper as agranulocytosis. Since Schultz, in 1922, gave an accurate description of a fulminat ing case, agranulocytosis has oomettoClOCo.'UPy more and more prominence in the medical field. Today, the literature is fairly teeming with accounts of isolated cases of all descriptions. Added to this a confus ing nomenclature, varied classifications, and heterogeneous forms of treatment; and the large question of whether it is a disease entity, a group of diseases, or only a symptom complex, and some idea may be garnered as to the progress made. Time is a most important factor in diagnosis of this disease, and the prognosis at best is grave. The treatment has gone through the maze of trials as that of any other new disease; there must be a cause and so there must be some specific treatment. -
Organs of the Immune System
ORGANS OF THE IMMUNE SYSTEM BY MRS. N .MAKANDI ORGANS OF THE IMMUNE SYSTEM Major organs of the immune system are bone marrow, thymus, spleen and lymph nodes. These organs produce lymphocytes required to destroy bacteria, virus, tumor cells, etc. NB// The function of the immune system is protecting the body from parasitic, bacterial, viral, fungal infections and from the growth of tumor cells. • Organs of the immune system make cells that either contribute in the immune response or act as sites for the immune function. There are two groups of immune system organs. • Primary (central) organs where immature lymphocytes develop – Thymus – Bone marrow • Secondary (peripheral) organs --tissues where antigen is localized so that it can be effectively exposed to mature lymphocytes – Lymph nodes – Spleen – MALT (Mucosal-Associated Lymphoid Tissue) • GALT (Gut-Associated Lymphoid Tissue) • BALT (Bronchial/Tracheal-Associated Lymphoid Tissue) • NALT (Nose-Associated Lymphoid Tissue) • VALT (Vulvovaginal-Associated Lymphoid Tissue) Primary (central) lymphoid organs Bone marrow • All the cells of the human immune system are formed in the bone marrow, found within the bones, by a process called hematopoiesis. • The process of hematopoiesis involves differentiation of bone-marrow derived stem cells either into mature cells of the immune system or precursor of cells which move out of the bone marrow and continue their maturation elsewhere. • The bone marrow is responsible for the production of important immune system cells like B cells, granulocytes, natural killer cells and immature thymocytes. It also produces red blood cells and platelets • Bone marrow is the site of B cell maturation. • The site of B cell maturation in birds is the bursa of Fabricius, after which B cells are named. -
Abstracts of the Nurses Group EBMT 2006
Abstracts of the Nurses Group EBMT 2006 and so decreases levels of anxiety and improves clinical Supportive care outcomes (Audit Commission 1993). Bone Marrow Transplantation (BMT) has been described as a procedure associated with isolation of the patient, prolonged N922 hospitalizations, rapid fluctuations in medical conditions, Nursing aspects in patient-information frequent and often life-threatening infections, and graft-versus- G. Rother, C. Weßler, N. Reebehn host disease (GvHD). UK-SH, Campus Kiel (Kiel,D) It is a complex process with immediate as well as long-term effects, which may permanently impair quality of life and can In addition to the information supplied by physicians there is affect morbidity and mortality. Achieving a level of also a need for explaining the nursing aspects to the patients. understanding of what is involved can be a bewildering Both sides are important to minimize fear, to create an proposition for many patients and their carers, and in itself can atmosphere of confidence and to help the patient complete present obstacles to informed consent and subsequent post- their treatment successfully. transplant expectations. A stay on the BMT-unit is not like any other time in hospital. The Seven Steps is a project which evolved through the need Lots of questions arise before admission and during the stay to meet our patients’ demand for accurate and clear written and patients often are left with a huge amount of uncertainty literature to support and compliment verbal description. The about what to do or not to do. During the preparations at the result is a book, which divides the bone marrow transplant outpatient clinic physicians inform their patients thoroughly journey into 7 clear steps, which provide a high level of detail about the medical side of the transplantation process but they yet with a strong patient focus. -
Human Anatomy and Physiology
LECTURE NOTES For Nursing Students Human Anatomy and Physiology Nega Assefa Alemaya University Yosief Tsige Jimma University In collaboration with the Ethiopia Public Health Training Initiative, The Carter Center, the Ethiopia Ministry of Health, and the Ethiopia Ministry of Education 2003 Funded under USAID Cooperative Agreement No. 663-A-00-00-0358-00. Produced in collaboration with the Ethiopia Public Health Training Initiative, The Carter Center, the Ethiopia Ministry of Health, and the Ethiopia Ministry of Education. Important Guidelines for Printing and Photocopying Limited permission is granted free of charge to print or photocopy all pages of this publication for educational, not-for-profit use by health care workers, students or faculty. All copies must retain all author credits and copyright notices included in the original document. Under no circumstances is it permissible to sell or distribute on a commercial basis, or to claim authorship of, copies of material reproduced from this publication. ©2003 by Nega Assefa and Yosief Tsige All rights reserved. Except as expressly provided above, no part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or by any information storage and retrieval system, without written permission of the author or authors. This material is intended for educational use only by practicing health care workers or students and faculty in a health care field. Human Anatomy and Physiology Preface There is a shortage in Ethiopia of teaching / learning material in the area of anatomy and physicalogy for nurses. The Carter Center EPHTI appreciating the problem and promoted the development of this lecture note that could help both the teachers and students. -
761070Orig1s000
CENTER FOR DRUG EVALUATION AND RESEARCH APPLICATION NUMBER: 761070Orig1s000 NON-CLINICAL REVIEW(S) Tertiary Pharmacology/Toxicology Review Date: November 1, 2017 From: Timothy J. McGovern, PhD, ODE Associate Director for Pharmacology and Toxicology, OND IO BLA: 761070 Agency receipt date: November 16, 2016 Drug: FASENRA (benralizumab) injection, for subcutaneous use Sponsor: AstraZeneca Pharmaceuticals LP Indication: Add-on maintenance treatment of patients with severe asthma aged 12 years and older, and with an eosinophilic phenotype. Reviewing Division: Division of Pulmonary, Allergy, and Rheumatology Products The primary pharmacology/toxicology reviewer and team leader concluded that the nonclinical data for FASENRA (benralizumab) solution for subcutaneous injection support approval for the indication listed above. Benralizumab is a humanized, afucosylated IgG1 kappa monoclonal antibody that targets interleukin-5 receptor alpha. The recommended dose of benralizumab is 30 mg administered once every 4 weeks for the first 3 doses, and then once every 8 weeks thereafter. The Established Pharmacologic Class (EPC) for benralizumab is “interleukin- 5 receptor alpha-directed cytolytic monoclonal antibody”. Pivotal nonclinical studies were conducted in Cynomolgus monkeys. In toxicology studies up to 39 weeks duration, NOAELs of 10 mg/kg IV and 30 mg/kg SC were identified. The primary finding at a dose of 25 mg/kg IV was a post-dose reaction in one high-dose female that included bruising in the areas of the eyes, face, chest and lower abdomen, a decrease in platelet counts, and abnormal erythrocytes after the fourth dose. The NOAEL doses were associated with systemic exposures (AUC) that provided 153- to 271-fold exposure margins compared to the recommended clinical dose. -
Bone Marrow.Pdf
Libyan International Medical University Faculty of Pharmacy Academic Year 2019-2020 OBJECTIVES 1. Define bone marrow 2. Illustrate where the bone marrow is found 3. Describe the components of bone marrow 4. Describe the types of bone marrow 5. Explain the functions of bone marrow What is Bone Marrow? ■ Bone marrow, also called myeloid tissue, is the soft, highly vascular and flexible connective tissue within bone cavities which serve as the primary site of new blood cell production or hematopoiesis. Where is the Bone Marrow found? ■ In a newborn baby's bones exclusively contain hematopoietically active "red" marrow, and there is a progressive conversion towards "yellow" marrow with age. ■ In adults, red marrow is found mainly in the central skeleton, such as the pelvis, sternum, cranium, ribs, vert ebrae and scapulae, and variably found in the proximal epiphyseal ends of long bones such as the femur and humerus. What are the components of Bone Marrow? ■ The bone marrow is composed of both cellular and non-cellular components and is structurally divided into vascular and non-vascular regions. ■ The non-vascular section of bone marrow is composed of hemopoietic cells of various lineages and maturity, packed between fat cells, thin bands of bony tissue (trabeculae), collagen fibers, fibroblasts and dendritic cells. This is where hematopoiesis takes place. ■ The vascular section contains blood vessels that supply the bone with nutrients and transport blood stem cells and formed mature blood cells away into circulation. ■ Ultrastructural studies show hemopoietic cells cluster around the vascular sinuses where they mature, before they eventually are discharged into the blood. -
Hematopoietic Stem Cells with High Proliferative Potential: ASSAY of THEIR CONCENTRATION in MARROW by the FREQUENCY and DURATION of CURE of W/Wv MICE
Hematopoietic Stem Cells with High Proliferative Potential: ASSAY OF THEIR CONCENTRATION IN MARROW BY THE FREQUENCY AND DURATION OF CURE OF W/Wv MICE Dane R. Boggs, … , Lora A. Gress, Don R. Canfield J Clin Invest. 1982;70(2):242-253. https://doi.org/10.1172/JCI110611. This study was designed to approach two primary questions concerning hematopoietic stem cells (HSC) in mice: what is the concentration of HSC with extensive proliferative potential in marrow, and how long can an HSC continue to function in an intact animal? The assay system was the W/Wv mouse, a mouse with an inherited HSC defect, reflected in a reduction in all myeloid tissue and most particularly in a macrocytic anemia. A single chromosomally marked HSC will reconstitute the defective hematopoietic system of the W/Wv. The concentration of HSC in normal littermate (+/+) marrow was assayed by limiting dilution calculation using cure of W/Wv as an end point (correction of anemia and erythrocytes' macrocytosis) and found to be ∼10/105. This is significantly less than spleen colony forming cell (CFU-S) concentration: ∼220/105 in +/+ and ranging from 50 to 270/105 in various other studies. Blood values were studied at selected intervals for as long as 26 mo. Of 24 initially cured mice, which were observed for at least 2 yr, 75% remained cured. However, of all cured mice, 17 lost the cure, returning to a macrocytic anemic state. Cured mice had normal numbers of nucleated and granulocytic cells per humerus and a normal concentration of CFU-S. However, cure of secondary W/Wv recipients by this marrow was inefficient compared with the original +/+ […] Find the latest version: https://jci.me/110611/pdf Hematopoietic Stem Cells with High Proliferative Potential ASSAY OF THEIR CONCENTRATION IN MARROW BY THE FREQUENCY AND DURATION OF CURE OF W/WV MICE DANE R. -
JOURNAL of CANCER a Continuation of the Journal of Cancer Research
THE AMERICAN JOURNAL OF CANCER A Continuation of The Journal of Cancer Research VOLUMEXXXVII SEPTEMBER,1939 NUMBER1 MYELOID LEUKEMIA AND NON-MALIGNANT EXTRAMEDULLARY MYELOPOIESIS IN MICE' W. A. BARNES, M.D., AND I. E. SISMAN, M.D. (From the Department of Pathology, Cornell University Medical College, New York) Lymphatic leukemia of mice has been extensively studied by many investi- gators (cf. 1, 2). The anatomical changes are well known and their differ- entiation from non-leukemic processes offers little or no difficulty. Myeloid leukemia is in most stocks of mice much less frequent than lymphoid leukemia (cf. Emile-Weil and Bousser, 1; Opie, 3). In the Slye stock, however, Simonds found 39 cases of myeloid and 28 of lymphatic leukemia in the first 15,000 autopsies. In our Stock Ak lymphoid leukemia is very common but myeloid leukemia is rare. Tn Stock Rf, on the other hand, myeloid leukemia occurs frequently but lymphoid leukemia is unusual. In Stock S both types are found, as well as atypical forms. It is not possible from the literature to give exact figures for the incidence of myeloid leukemia because, thus far, it has not been sharply separated from non-malignant extramedullary myelo- poiesis. Simonds (4), who first extensively studied leukemia in mice, states: I' It was necessary to differentiate myelogenous leukemia in mice from an inflammatory leukocytosis. In the latter condition, a focus of acute infection could frequently be found in some organ, such as pneumonia, an abscess or a pyelitis. In such infections the blood was frequently remarkably rich in nucleated cells and these might almost equal the number seen in myelogenous leukemia. -
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THE OXYDASE OF MYELOID TISSUE and THE USE OF . THE OXYDASE REACTION IN THE DIFFERENTIATION OF ACUTE LEUIIAEMIAS. by JOHN SHAW DUNN, M.A. , M.B., Ch.B. ProQuest Number: 27626761 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a com plete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 27626761 Published by ProQuest LLO (2019). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States C ode Microform Edition © ProQuest LLO. ProQuest LLO. 789 East Eisenhower Parkway P.Q. Box 1346 Ann Arbor, Ml 48106- 1346 1 - PRELIMINARY. The oxidising property of leucocytes was pointed out by Vitali (1887)^^, when he showed that pus added to tincture of guaiacum produced guaiac-blue, without the addition of hydrogen peroxide. He found that the reaction did not take place if the pus were previously boiled, thus showing that the oxygenating substance was thermo-labile. Brandenburg (1900)^, in a further investigation of this subject, was able, by extracting pus with chloroform water and precipitat ing with alcohol, to obtain a powder which possessed the oxidising property in a marked degree. He considered it to be of the nature of a ferment, and to have the con stitution of a nucleo-albumin. It could be obtained readily from organs vhich contained abundant granular leucocytes, such as bone marrow, but not from purely lymphocytic organs, such as lymphatic glands or thymus, nor from normal liver. -
Original Article HAEMATOPOIETIC THROMBOCYTE PRECURSORS
Bulgarian Journal of Veterinary Medicine, 2021, 24, No 1, 2231 ISSN 1311-1477; DOI: 10.15547/bjvm.2019-0063 Original article HAEMATOPOIETIC THROMBOCYTE PRECURSORS IN RAT FEMORAL AND STERNAL BONE MARROW D. SULJEVIĆ1, A. HAMZIĆ1, E. ISLAMAGIĆ1, E. FEJZIĆ2 & A. ALIJAGIĆ1 1Department of Biology, Faculty of Science, University of Sarajevo, Sarajevo, Bosnia and Herzegovina; 2Institute for Transfusion Medicine of FBiH, Sarajevo, Bosnia and Herzegovina Summary Suljević, D., A. Hamzić, E. Islamagić, E. Fejzić & A. Alijagić, 2021. Haematopoietic thrombocyte precursors in rat femoral and sternal bone marrow. Bulg. J. Vet. Med., 24, No 1, 2231. This research presents the first findings on thrombopoiesis for Wistar rats. Haemopoietic cells from the femur and the sternum were analysed by light microscopy in combination with infrared and near- ultraviolet light for fine cytoplasmic structure analysis. Five main types of thrombocyte precursor cells were identified in the bone marrow samples: megakaryoblast, promegakaryocyte and megakaryocyte (basophilic, acidophilic and thrombocytogenic). More intensive thrombopoiesis and morphologically differentiated cells were found in sternum samples. Key words: bone marrow, megakaryocyte, platelets, thrombopoiesis, Wistar rat INTRODUCTION Bone marrow smears from rats usually is diminished as platelets production is contain a large number of megakaryocytes shifted from the spleen to some other accounting for 0.40–0.77% of total organ, like bone marrow (Bolliger, 2004). nucleated cells in rat bone marrow (Saad Large megakaryocytes could be a et al., 2000). Density and distribution of product of an early thrombopoietic phase megakaryocytes vary with technique and occurring in the first days of pregnancy as among smears; however, there are no observed in the mammalian order of published results regarding the precise rodents (Rodentia) (Pacheco et al., 2002). -
Platelet and Erythrocyte Functional Defects Caused by Mutations of Transcription Factor GFI1B
Platelet and erythrocyte functional defects caused by mutations of transcription factor GFI1B Lucinda Beutler A thesis submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Faculty of Medicine University of Sydney December 2018 I praise you because…… I am fearfully and wonderfully made; Your works are wonderful - I know that full well. Psalm 139:14 (NIV) TABLE OF CONTENTS STATEMENT OF ORIGINALITY ...................................................................................................... vi ACKNOWLEDGEMENTS .............................................................................................................. vii ABSTRACT ................................................................................................................................... ix PUBLICATIONS AND PRESENTATIONS ........................................................................................... x LIST OF FIGURES .......................................................................................................................... xi LIST OF TABLES........................................................................................................................... xv ABBREVIATIONS ........................................................................................................................ xvii 1. Literature review ...................................................................................................................... 2 1.1 Introduction ...................................................................................................................... -
Aandp1ch07lecture.Pdf
Chapter 07 Lecture Outline See separate PowerPoint slides for all figures and tables pre- inserted into PowerPoint without notes. Copyright © McGraw-Hill Education. Permission required for reproduction or display. 1 Introduction • In this chapter we will cover: – Bone tissue composition – How bone functions, develops, and grows – How bone metabolism is regulated and some of its disorders 7-2 Introduction • Bones and teeth are the most durable remains of a once-living body • Living skeleton is made of dynamic tissues, full of cells, permeated with nerves and blood vessels • Continually remodels itself and interacts with other organ systems of the body • Osteology is the study of bone 7-3 Tissues and Organs of the Skeletal System • Expected Learning Outcomes – Name the tissues and organs that compose the skeletal system. – State several functions of the skeletal system. – Distinguish between bones as a tissue and as an organ. – Describe the four types of bones classified by shape. – Describe the general features of a long bone and a flat bone. 7-4 Tissues and Organs of the Skeletal System • Skeletal system—composed of bones, cartilages, and ligaments – Cartilage—forerunner of most bones • Covers many joint surfaces of mature bone – Ligaments—hold bones together at joints – Tendons—attach muscle to bone 7-5 Functions of the Skeleton • Support—limb bones and vertebrae support body; jaw bones support teeth; some bones support viscera • Protection—of brain, spinal cord, heart, lungs, and more • Movement—limb movements, breathing, and other