RBC Morphology Normal RBC Morphology
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Age-Related Features and Pathology of Blood in Children
MINISTRY OF PUBLIC HEALTH OF UKRAINE HIGHER STATE EDUCATIONAL ESTABLISHMENT OF UKRAINE «UKRAINIAN MEDICAL STOMATOLOGICAL ACADEMY» V.I. POKHYLKO, S.M. TSVIRENKO, YU.V. LYSANETS AGE-RELATED FEATURES AND PATHOLOGY OF BLOOD IN CHILDREN MANUAL FOR STUDENTS OF HIGHER MEDICAL EDUCATIONAL INSTITUTIONS OF THE III-IV ACCREDITATION LEVELS Poltava 2017 МІНІСТЕРСТВО ОХОРОНИ ЗДОРОВ’Я УКРАЇНИ ВИЩИЙ ДЕРЖАВНИЙ НАВЧАЛЬНИЙ ЗАКЛАД УКРАЇНИ «УКРАЇНСЬКА МЕДИЧНА СТОМАТОЛОГІЧНА АКАДЕМІЯ» ПОХИЛЬКО В.І., ЦВІРЕНКО С.М., ЛИСАНЕЦЬ Ю.В. ВІКОВІ ОСОБЛИВОСТІ ТА ПАТОЛОГІЯ КРОВІ У ДІТЕЙ НАВЧАЛЬНИЙ ПОСІБНИК ДЛЯ СТУДЕНТІВ ВИЩИХ МЕДИЧНИХ НАВЧАЛЬНИХ ЗАКЛАДІВ III-IV РІВНІВ АКРЕДИТАЦІЇ Полтава 2017 2 UDC: 616+616.15]-053.2(075.8) ВВС: 57.33я73 The manual highlights the issues of embryogenesis, age-related features, semiotics of lesion, examination methods and diseases of hemic system in children. The manual is intended for students of higher educational institutions of III-IV accreditation levels, and can be used by medical interns and primary care doctors. Authors: Doctor of Medical Sciences, Professor of the Department of Pediatrics No.1 with Propedeutics and Neonatology V.I. Pokhylko Candidate of Medical Sciences, Acting Head of the Department of Pediatrics No.1 with Propedeutics and Neonatology S.M. Tsvirenko Candidate of Philological Sciences, Senior Lecturer of the Department of Foreign Languages with Latin and Medical Terminology Yu.V. Lysanets Reviewers: O.S. Yablon’ ― Doctor of Medical Sciences, Professor, Head of the Department of Pediatrics No.1, Vinnytsya National M.I. Pirogov Memorial Medical University of Ministry of Public Health of Ukraine. M.O. Honchar ― Doctor of Medical Sciences, Professor, Head of the Department of Pediatrics and Neonatology No.1, Kharkiv National Medical University. -
Anormal Rbc in Peripheral Blood. [Repaired].Pdf
1. Acanthocyte 2. Burr-cell 3. Microcyte 1. Basophilic Normoblast 2. Polychromatic Normoblast 3. Pycnotic Normoblast 4. Plasmocyte 5. Eosinophil 6. Promyelocyte 1. Macrocyte 2. Elliptocyte 1. Microcyte 2. Normocyte 1. Polychromatic Erythrocyte 2. Acanthocyte 3. Elliptocyte 1. Polychromatic Normoblast 2. Pycnotic Normoblast 3. Neutrophil Myelocyte 4. Neutrophil Metamyelocyte 1. Schistocyte 2. Microcyte BASOPHILIC ( EARLY ) NORMOBLASTS Basophilic Erythroblast Basophilic Stippling, Blood smear, May-Giemsa stain, (×1000) CABOT'S RINGS Drepanocyte Elliptocyte Erythroblast ERYTHROBLAST in the blood Howell-jolly body Hypo chromic LACRYMOCYTES Leptocyte Malaria, Blood smear, May-Giemsa stain, ×1000 MICROCYTES Orthochromatic erythroblast Pappen heimer Bodies & 1. Schistocyte 2. Elliptocyte 3. Acanthocyte POIKILOCYTOSIS Polychromatic Erythroblast Pro Erytroblast Proerythroblasts Reticulocyte Rouleaux SICKLE CELLS Sickle cell Spherocyte Spherocyte Spherocyte SPHEROCYTES STOMATOCYTES Target Cells Tear Drop Cell, Blood smear, May-Giemsa stain, x1000 Anulocyte 1. Burr-cell 2. Elliptocyte 1. Macrocyte 2. Microcyte 3. Elliptocyte 4. Schistocyte 1. Ovalocyte 2. Lacrymocyte 3. Target cell 1. Polychromatic Erythrocyte 2. Basophilic Stippling 1. Proerythroblast 2. Basophilic Erythroblast 3. Intermediate Erythroblast 4. Late Erythroblast 5. Monocyte 6. Lymphocyte 1. Target-cell 2. Elliptocyte 3. Acanthocyte 4. Stomatocyte 5. Schistocyte 6. Polychromatophilic erythrocyte. 1.Pro erythroblast 2.Basophilic normoblast 3.Polychromatic normoblast 4.Pycnotic normoblast -
20 Hemolytic Anemias Due to Abnormal Red Cell Enzymes
Hemolytic Anemias Due to Abnormal Red Cell Enzymes MODULE Hematology and Blood Bank Technique 20 HEMOLYTIC ANEMIAS DUE TO Notes ABNORMAL RED CELL ENZYMES 20.1 INTRODUCTION The main metabolic substrate for the RBCs is glucose. It is metabolized by two pathways: approximately 90% of the glucose is metabolized through the Embden Meyerhoff (glycolytic) pathway and the rest by the hexose monophosphate (HMP) pathway. In the Embden Meyerhoff (glycolytic) pathway glucose is metabolized to lactate through a series of enzymatic steps. Each molecule of glucose gives rise to 2 molecules of ATP. The ATP provides energy to maintain red cell volume, shape and flexibility. An ATP dependent pump in the red cell membrane actively keeps sodium out of the cell and potassium inside. The red cell has the enzymes that are needed for the glycolytic pathway. These enzymes help break down glucose to generate ATP which is the source of energy. About 10% of the glucose is diverted to the Hexose Monophosphate shunt pathway and this is essential for protection of red cells from oxidative stress. This pathway is necessary for the generation of NADPH which then reduces oxidized glutathione (GSSG) to reduced glutathione (GSH). GSH prevents the accumulation of H2O2 and the oxidation of hemoglobin to methemoglobin. When the level of GSH falls, H2O2 accumulates in the cell and oxidizes the hemoglobin to methemoglobin which becomes denatured and precipitates as Heinz bodies. These inclusions are rigid and attached to the red cell membrane and make the red cell susceptible to hemolysis. The NADPH required in this pathway is generated by the enzyme Glucose 6 phosphate dehydrogenase (G6PD). -
SEED Haematology Sysmex Educational Enhancement and Development October 2012
SEED Haematology Sysmex Educational Enhancement and Development October 2012 The red blood cell indices The full blood count has been used in conjunction with the traditional red The complete blood count (CBC) is central to clinical deci- cell indices in order to narrow down the possible causes sion making. This makes it one of the commonest laboratory of anaemia in an individual patient. investigations performed worldwide. Whilst the definition of what constitutes an CBC is influenced by the number Impedance technology and type of parameters measured by different haematology The RBC, HCT and MCV are all closely interrelated as they analysers, the traditional red cell indices that are widely are derived from information obtained from the passage used to classify anaemias are common to all. of cells through the aperture of the impedance channel of an automated haematology analyser. The impedance The laboratory approach to anaemia technology is based on the principle that an electrical field, Anaemia is an extremely common global healthcare prob- created between two electrodes of opposite charge, can lem. However, anaemia is merely a symptom which can be used to count and determine the size of cells. Blood result from a multitude of causes. Effective treatment is cells are poor conductors of electricity. The diluent in which only possible if the underlying cause is correctly identified. they are suspended as they pass through the aperture To this end, several classification systems have been devis- during counting is an isotonic solution which is a good ed. The most useful and widely used classification system conductor of electricity. -
The Widespread Application of Red Cell Survival Sive Red
CLINICAL DETERMINATION OF THE SITES OF RED CELL SEQUESTRATION IN HEMOLYTIC ANEMIAS1 By JAMES H. JANDL, MORTIMER S. GREENBERG, ROBERT H. YONEMOTO, AND WILLIAM B. CASTLE (From the Thorndike Memorial Laboratory and Second and Fourth (Harvard), Medical Services Boston City Hospital, and the Department of Medicine, Harvard Medical School, Boston, Mass.) (Submitted for publication January 30, 1956; accepted April 3, 1956) The widespread application of red cell survival greater than that of other tissues even when cor- techniques has revealed the importance of exces- rection was made for the Cr5l activity of the re- sive red cell destruction in the pathologic physi- sidual red cells. Moreover, the radioactivity of ology of many of the anemias. An increasing ar- the packed red cells removed from the spleen ex- ray of in vitro methods for detecting red cell or ceeded that of a comparable sample of packed red serum abnormalities has provided insight into the cells from the peripheral blood. In order to in- in vivo mechanisms underlying some of these proc- vestigate the possibility that Cr51-labelled red cell esses. In certain disease states the presence of deposition could be determined by measuring body visible or physically measurable alterations of the surface radioactivity, several questions required red cells has permitted detection of the sites and exploration: 1) Are the emanations of Cr5 suit- to some extent of the mechanisms of sequestration able for external body scanning at safe dosage of these cells. Such valuable observations have levels? 2) Does the site of tissue deposition of been made upon pathologic material from patients Cr65 following the intravenous injection of Cr51- with congenital hemolytic anemia (1-5) and labelled red cells necessarily indicate the site of sickle cell anemia (1, 5-7). -
Red Blood Disorders Anemia Med.Pdf 14.44MB
Lviv National Medical University Department of pathological physiology PATHOLOGY OF RED BLOOD PhD. Sementsiv N.G. In norm The number of erythrocytes: in female - 3,9-4,7·1012/l in male - 4,5-5,0·1012/l Hemoglobin in female - 120-140g/l in male - 140-160g/l Color index(CI) - 0,85-1,15 Globular value = 3 x Hb / the first 3 figures of erythrocytes. Reticulocytes - 0.5-2%, 0,5-2%0 changes in total blood volume normovolemia hypovolemia hypervolemia simple (Ht - norm), polycitemia (Ht > 0,48), olygocytemia (Ht < 0,36). A) Norm B) acut anaemia б) acute hemorrhage г) hydremia Pathological forms of erythrocytes regenerative degenerative cell pathologic regeneration Regenerative forms reticulocytes залежно від зрілості розрізняють: (Зернисті) Stippling (Сітчасті) Mesh Norm in a blood reticulocytes - 0,2–2,0%. Regenerative forms Basophiles substantial erythrocytes - cytoplasm remains basophilic normo blast. Polychromatophil erythrocytes (polychromasia, polychromatophilia ) – erythrocytes with basophiles substantial ( blue cells) indicates increased RBC production by the marrow Qualitative (degenerative) changes of red blood cell - poikilocytosis - different shape of erythrocytes; - anisocytosis - different size of erythrocytes; - anisochromia - different saturation of red blood cells by hemoglobin Degenerative forms Anisocytosis present in a blood different forms erythrocytes » normocyte (7,01–8,0 мкм) » microcyte(6,9–5,7 мкм) » macrocyte(8,1–9,35 мкм) » megalocyte (10–15 мкм) Degenerative forms Poikilocytosis present in a blood pictures erythrocytes different forms : elongate form , oval, ellipsoid and os. ОVAlOCYTE( ELLIPTOCYTE) – 5% all blood. Pathological cells regenerate Megaloblast mehaloblastyc cell type hematopoiesis Megaloblast oval cells in the diameter of 1,5- 2,0 times larger than normal erythrocytes is the final stage mehaloblastyc hematopoiesis. -
Cambridge University Press 978-0-521-51426-2 — Anemia with Online Resource Edited by Edward J
Cambridge University Press 978-0-521-51426-2 — Anemia with Online Resource Edited by Edward J. Benz, Jr. , Nancy Berliner , Fred J. Schiffman Index More Information Index aAA. See acquired aplastic clinical significance of, 187 through RBC transfusion, anemia of inflammation, 169 anemia dementia, 187 175 anemia of prematurity, 34 abdomen, physical examination epidemiology of, 185–6 with rhEPO, 172, 174–7 anemias. See also clinical of, 32 inflammation and, 186–7 pathogenesis of, 172–3 approaches; specific ABO incompatibility, 36 hepcidin levels, 186 pathophysiology, 198 anemias HSCT and, 181 leptin protein, 186 therapy-related toxicity causes of, xi, 1 acanthocytes, 27 MIF, 186 grading, 172 through blood loss, 24 ACD. See anemia of chronic TNF-α, 186 transfusion, 175 classification of, 24 inflammation vitamin D deficiency, 186–7 anemia of chronic inflammation through MCV, 24 ACI. See anemia of chronic management strategies, 187–8 (ACI) clinical definitions of, xi, 23 inflammation prevalence of, 185 cancer and, 172 comorbidities with, xi acquired aplastic anemia (aAA), aHUS. See atypical hemolytic case study for, 153–4 defined, 172, 185 128–32. See also uremic syndrome clinical presentation, 152–3, diagnostic approach, 23–4 paroxysmal nocturnal AIHA. See autoimmune 194 through bone marrow hemoglobinuria hemolytic anemia critical illness with, 151 aspirate specimens, 24 bone marrow with, 128 alcohol use, non-megaloblastic cytokines, 196 through peripheral blood clinical presentation of, 129 macrocytic anemias diagnostic evaluation, 153, smears, 24–5, 29 clonal hematopoiesis and, 129 from, 63 194–5 future approaches to, 230–3 diagnostic evaluation of, alemtuzumab, 134 epidemiology, 150–1 hemoglobin deficiency in, xi 129–30 ALI. -
10 11 Cyto Slides 81-85
NEW YORK STATE CYTOHEMATOLOGY PROFICIENCY TESTING PROGRAM Glass Slide Critique ~ November 2010 Slide 081 Diagnosis: MDS to AML 9 WBC 51.0 x 10 /L 12 Available data: RBC 3.39 x 10 /L 72 year-old female Hemoglobin 9.6 g/dL Hematocrit 29.1 % MCV 86.0 fL Platelet count 16 x 109 /L The significant finding in this case of Acute Myelogenous Leukemia (AML) was the presence of many blast forms. The participant median for blasts, all types was 88. The blast cells in this case (Image 081) are large, irregular in shape and contain large prominent nucleoli. It is difficult to identify a blast cell as a myeloblast without the presence of an Auer rod in the cytoplasm. Auer rods were reported by three participants. Two systems are used to classify AML into subtypes, the French- American-British (FAB) and the World Health Organization (WHO). Most are familiar with the FAB classification. The WHO classification system takes into consideration prognostic factors in classifying AML. These factors include cytogenetic test results, patient’s age, white blood cell count, pre-existing blood disorders and a history of treatment with chemotherapy and/or radiation therapy for a prior cancer. The platelet count in this case was 16,000. Reduced number of platelets was correctly reported by 346 (94%) of participants. Approximately eight percent of participants commented that the red blood cells in this case were difficult to evaluate due to the presence of a bluish hue around the red blood cells. Comments received included, “On slide 081 the morphology was difficult to evaluate since there was a large amount of protein surrounding RBC’s”, “Slide 081 unable to distinguish red cell morphology due to protein” and “Unable to adequately assess morphology on slide 081 due to poor stain”. -
Pathological Physiology
PATHOLOGICAL PHYSIOLOGY PRACTICAL PART Student _____________________________ Group number ________________________ Teacher _____________________________ Minsk BSMU 2015 МИНИСТЕРСТВО ЗДРАВООХРАНЕНИЯ РЕСПУБЛИКИ БЕЛАРУСЬ БЕЛОРУССКИЙ ГОСУДАРСТВЕННЫЙ МЕДИЦИНСКИЙ УНИВЕРСИТЕТ КАФЕДРА ПАТОЛОГИЧЕСКОЙ ФИЗИОЛОГИИ ПАТОЛОГИЧЕСКАЯ ФИЗИОЛОГИЯ PATHOLOGICAL PHYSIOLOGY Практикум 4-е издание Минск БГМУ 2015 2 УДК 616-092.18(811.111)-054.6(076.5) (075.8) ББК 52.52 (81.2 Англ-923) П20 Рекомендовано Научно-методическим советом университета в качестве практикума 16.09.2015 г., протокол № 1 Авторы: Ф. И. Висмонт, В. А. Касап, С. А. Жадан, А. А. Кривчик, Е. В. Леонова, Т. В. Короткевич, Л. С. Лемешонок, А. В. Чантурия, Т. А. Афанасьева, В. Ю. Перетятько, О. Г. Шуст, Н. А. Степанова, К. Н. Грищенко, Э. Н. Кучук, Д. М. Попутников, Е. В. Меленчук Рецензенты: член-корр. НАН Беларуси, д-р мед. наук, проф. каф. нормальной физиологии Л. М. Лобанок; д-р мед. наук, проф. каф. патологической анатомии М. К. Недзьведзь Патологическая физиология = Pathological physiology : практикум / Ф. И. Вис- П20 монт [и др.]. – 4-е изд. – Минск : БГМУ, 2015. – 191 с. ISBN 978-985-567-304-1. Содержит описания и протоколы оформления лабораторных работ по основным разделам кур- са патофизиологии. Представлена информация по следующим разделам: патофизиология системы крови, нарушение сердечного ритма, кислотно-основного состояния, наследственности и изменчи- вости организма. Первое издание вышло в 2010 году. Предназначен для студентов 2–3-го курсов медицинского факультета иностранных учащихся для самостоятельной подготовки к занятиям, выполнения и оформления лабораторных работ по предмету. УДК 616-092.18(811.111)-054.6(076.5) (075.8) ББК 52.52 (81.2 Англ-923) ISBN 978-985-567-304-1 ã УО «Белорусский государственный медицинский университет», 2015 3 SECTION I GENERAL NOSOLOGY LESSON 1. -
Immunohematology JOURNAL of BLOOD GROUP SEROLOGY and EDUCATION
Immunohematology JOURNAL OF BLOOD GROUP SEROLOGY AND EDUCATION VOLUME 17, NUMBER 1, 2001 From the publishers of Immunohematology A Comprehensive Laboratory Manual Immunohematology Methods and Procedures Featuring— • Over 100 methods— just about every method used in a reference lab. • Eleven chapters discussing problems faced by blood group serologists and the procedures and methods that can be used to solve them. • An extra set of the methods to use at the bench, printed on durable waterproof paper. • See business reply order card enclosed in this issue or order on the Web at redcross.org/immunohematology Now available from Montgomery Scientific Publications APPLIED BLOOD GROUP SEROLOGY, 4th EDITION by Peter D. Issitt and David J. Anstee A totally revised, mostly rewritten, fully up-to-date edition of one of the most popular books about the blood groups and blood transfusion ever published. I 46 chapters, an increase of 16 over the third edition 1 ″× ″ • 1,208 plus xxiv 8 /2 11 pages, hardbound, fully indexed, over 1,500 entries I 260 tables and 112 figures, an increase of more than 60% over the third edition • Over 13,500 references, more than 5,000 are papers written since 1985 Prices; each includes shipping: USA $125.00; Canada/International $130.00 (surface mail); International $170.00 (air mail). ALL ORDERS MUST BE PREPAID (Check or Credit Card) in U.S. DOLLARS International orders by check drawn on a bank in the USA or by credit card please. Order from: Montgomery Scientific Publications, P.O. Box 2704, Durham, NC 27715, U.S.A. Credit card orders accepted by fax at (919) 489-1235 (No phone orders, please.) We accept VISA,MasterCard, and Discover Card. -
SUMMARY STATISTICS EQA Round: DIF2/21 - Peripheral Blood Morphology Evaluation Deadline (EQA Round Closed): 28.05.2021 Key: ELG
SEKK SUMMARY STATISTICS EQA round: DIF2/21 - Peripheral Blood Morphology Evaluation Deadline (EQA round closed): 28.05.2021 Key: ELG ... expert laboratories group > ... possible result (found by ELG, but consensus not reached) AV, >>> ... assigned value type CVE (consensus of ELG) RAR ... range of acceptable results RoM ... robust average of all results Sample A Sample B AV RAR RoM AV RAR RoM WBC - differential count Blasts 0 0,000 - 0,018 0,000 0 0,000 - 0,018 0,000 Promyelocytes 0 0,000 - 0,018 0,000 0 0,000 - 0,018 0,000 Neutrophil myelocytes 0 0,000 - 0,018 0,000 0 0,000 - 0,018 0,000 Neutrophil metamyelocytes 0 0,000 - 0,018 0,000 0 0,000 - 0,018 0,000 Neutrophil bars 0,0010,000 - 0,018 0,003 0,0020,000 - 0,018 0,004 Segmented neutrophil granulocytes 0,5550,483 - 0,625 0,579 0,5750,503 - 0,644 0,584 Eosinophils - immature forms 0 0,000 - 0,018 0,000 0 0,000 - 0,018 0,000 Eosinophil segmented granulocytes 0,0690,039 - 0,115 0,060 0,0160,003 - 0,043 0,018 Basophilic granulocytes 0,0110,001 - 0,036 0,011 0,0070,000 - 0,028 0,007 Monocytes 0,0660,035 - 0,109 0,067 0,0640,035 - 0,109 0,059 Lymphocytes 0,2980,237 - 0,369 0,278 0,3310,265 - 0,400 0,326 Plasma cells 0 0,000 - 0,018 0,000 0 0,000 - 0,018 0,000 Erythroblasts (number) 0 0,000 - 2,000 0,000 0 0,000 - 3,000 0,002 Sample A Sample B WBC - morphology 23 No changes 15 % >>> 89 No changes 59 % 4 Hypergranulation/toxic granulation 2,6 % 2 Hypergranulation/toxic granulation 1,3 % 10 Agranulation 6,6 % 2 Agranulation 1,3 % > 78 Hypersegmented granulocytes 52 % 3 Hypersegmented granulocytes 2,0 % 6 Atypical/reactive/pathological monocytes/promono. -
Erythronoclastic) Anaemias of Later Infancy and Childhood: with Special Reference to the Acute Heemolytic Anemia of Lederer and the Anvemia of Von Jaksch
Arch Dis Child: first published as 10.1136/adc.8.45.184 on 1 June 1933. Downloaded from Part V.-The hamolytic (erythronoclastic) anaemias of later infancy and childhood: with special reference to the acute heemolytic anemia of Lederer and the anvemia of von Jaksch BY LEONARD G. PARSONS, M.D., F.R.C.P., AND J. C. HAWKSLEY, M.D., M.R.C.P. The destructive diseases of the erythron which fall for consideration under this heading show many points of general similarity although individual variations are frequent. In Part IV emphasis has been laid upon the fact that the erythron may be affected adversely either in the bone marrow or in the circulation; further, that for this reason the term haemolytic anaemia was probably incorrect because it stressed the destruction of red blood cells, but that the title of erythronoclastic ansemia was more correct http://adc.bmj.com/ because it indicated that the erythron may be affected in the circulation or in the marrow or in both situations. Moreover, this is not the whole story, because not only may the erythron itself be affected in either the circulation, the marrow or both, but also the other elements of the blood, the thrombocyte system and the myeloid leucocyte system, may suffer damage. in child's of iron Again, the latter months of the lactation period the supply on September 27, 2021 by guest. Protected copyright. for haemoglobin-building is somewhat precarious; a disturbance of the erythron is therefore likely to render manifest any iron deficiency and thus a deficiency anaemia may develop in the course of a haemolytic ansemia.