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Journal articles on the topic 'Anemia syndrome'

Author: Grafiati

Published: 28 May 2022

Last updated: 30 July 2025

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1

T., Glebova,. "Anemic Syndrome in Children in the Children’s Regional Hospital." Bulletin of Science and Practice, no. 1 (January 15, 2023): 197–99. http://dx.doi.org/10.33619/2414-2948/86/26.

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The study of a general blood test determining the nature of anemic syndrome in young children (0-12 years old) and children (3-6 years old) with infectious processes in the infectious department of the Penza Regional Children's Hospital was carried out. In the study, 4 groups were identified according to blood parameters in the age group 0-12 years. The study of the indicators of the general blood test showed that the first group cannot be attributed to the manifestations of severe anemia syndrome. In the second – normochromic, normocytic anemia syndrome. The third group had a manifestation of

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2

Gopchuk, O. M. "Iron deficiency anemia." HEALTH OF WOMAN, no. 9(145) (November 30, 2019): 32–37. http://dx.doi.org/10.15574/hw.2019.145.32.

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Iron deficiency anemia is the most common group of blood diseases in the population (80–95% of all anemias), characterized by a decrease in the number of circulating red blood cells and / or hemoglobin per unit volume of blood below normal for a given age and sex. The article deals with the role of iron in the human body, the conditions associated with its deficiency, causes, clinical symptoms, diagnosis of this pathology. Recommendations are given for the treatment of iron deficiency anemia by modern iron preparations, the advantages of using in the complex correction of heme iron deficiency,

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3

Lazrak FZ, Jahdaoui Adil, Yahyaoui Hicham, Ait Ameur Mustapha, and Chakour Mohamed. "Macrocytic anemia: Myelogram results in military hospital Avicenna in Marrakech." GSC Advanced Research and Reviews 13, no. 3 (2022): 212–15. http://dx.doi.org/10.30574/gscarr.2022.13.3.0275.

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Anemia is one of the most common health problems in the primary care setting. Macrocytosis in adults is defined as a red blood cell mean corpuscular volum >95 fL. Macrocytic anemias are generally classified into megaloblastic or non-megaloblastic anemia. Retrospective descriptive study included 340 samples of myelogram received in the Hematology Labortory belonging to patients admitted to the Military hospital of Avicenna in Marrakech, over a period of 48 months (from January 2016 to January 2020), aimed to assess the etiological profile of macrocytic anemia in patients whose bone marrow sm

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Lazrak, FZ, Adil Jahdaoui, Hicham Yahyaoui, Ameur Mustapha Ait, and Mohamed Chakour. "Macrocytic anemia: Myelogram results in military hospital Avicenna in Marrakech." GSC Advanced Research and Reviews 13, no. 3 (2022): 212–15. https://doi.org/10.5281/zenodo.7678386.

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Anemia is one of the most common health problems in the primary care setting. Macrocytosis in adults is defined as a red blood cell mean corpuscular volum >95 fL. Macrocytic anemias are generally classified into megaloblastic or non-megaloblastic anemia. Retrospective descriptive study included 340 samples of myelogram received in the Hematology Labortory belonging to patients admitted to the Military hospital of Avicenna in Marrakech, over a period of 48 months (from January 2016 to January 2020), aimed to assess the etiological profile of macrocytic anemia in patients whose bone marrow sm

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5

Mamchenko, I. L., E. G. Malaeva, Z. V. Grekova, O. A. Yarmolenko, I. A. Vasyukhina, and N. V. Kholupko. "Anemia syndrome of complex genesis." Health and Ecology Issues 19, no. 2 (2022): 134–39. http://dx.doi.org/10.51523/2708-6011.2022-19-2-17.

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Anemia is a clinical and hematological syndrome which is one of the most common diseases in the world. The clinical manifestations of anemia syndrome can be caused by both anemia itself and various manifestations of hypoxia and hypercapnia. Due to the similarity of the clinical manifestations, doctors of various specialties face a difficult task of the differential diagnosis of anemias and the selection of therapeutic tactics.The article presents a clinical case of anemia syndrome in a patient with comorbid pathology and latent vascular malformation. The presence of comorbid diseases in the pa

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6

Klimov, L. Ya, R. A. Zhetishev, T. A. Ivenskaya, et al. "PATHOGENETIC ASPECTS OF THE FORMATION OF ANEMIA IN CHILDREN WITH CELIAC DISEASE." Pediatria. Journal named after G.N. Speransky 101, no. 6 (2022): 116–25. http://dx.doi.org/10.24110/0031-403x-2022-101-6-116-125.

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Celiac disease (CD) is characterized by the formation of an anemic syndrome whose etiopathogenesis if of a multifactorial origin. The main types of anemias in children with celiac disease are iron deficiency anemia (IDA) and anemia of inflammation, also called anemia of chronic disease (ACD). This bibliographical review presents current information on the iron metabolism, morphological changes in the epithelium of the intestinal mucosa in celiac disease leading to the development of iron deficiency, pathogenesis of ACD formation in celiac disease, as well as the diagnosis of IDA and ACD in cel

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7

Urbanovych, A. M., and M. V. Yuskiv. "Peculiarities of the anemic syndrome course with thyroid dysfunction." INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (Ukraine) 19, no. 5 (2023): 391–97. http://dx.doi.org/10.22141/2224-0721.19.5.2023.1304.

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This article was created on the basis of a literature review in the Web of Science, PubMed and Scopus databases and analyzes information on the prevalence, classification, etiopathogenetic mechanisms of anemia, evaluation of data from clinical studies and meta-analyses on the course of anemic syndrome in thyroid diseases. Anemia and thyroid dysfunction are common phenomena that often occur simultaneously. According to modern recommendations, it is worth evaluating the function of the thyroid gland when investigating anemia. With thyroid dysfunction, normocytic anemia is the most common, and mi

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8

Pavliukovych, N. D., O. V. Pavliukovych, and V. O. Shuper. "Structure of Anemic Syndrome in Patients with Chronic Forms of Coronary Artery Disease." Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 7, no. 6 (2022): 95–99. http://dx.doi.org/10.26693/jmbs07.06.095.

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The purpose of the study was to determine the incidence and characteristic features of anemia in elderly and senile patients with chronic forms of coronary artery disease. Materials and methods. 1,993 case reports of patients with chronic forms of coronary artery disease with comorbid anemia were analyzed retrospectively. All patients were diagnosed with chronic coronary artery disease (stable angina pectoris of II-III functional classes, diffuse or focal (post-infarction) cardiosclerosis). Average age of investigated patients was 79.5 ± 5.24. Comorbid anemia was diagnosed in case of hemoglobi

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9

Alter, Blanche P. "Diagnosis, Genetics, and Management of Inherited Bone Marrow Failure Syndromes." Hematology 2007, no. 1 (2007): 29–39. http://dx.doi.org/10.1182/asheducation-2007.1.29.

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Abstract The inherited bone marrow failure syndromes are traditionally considered to be pediatric disorders, but in fact, many of the patients now are diagnosed as adults, and many diagnosed as children now live to reach adulthood. The most common of these rare disorders include Fanconi anemia, dyskeratosis congenita, Shwachman-Diamond syndrome and amegakaryocytic thrombocytopenia, which often develop aplastic anemia and may evolve into myelodysplastic syndrome and acute myeloid leukemia; and Diamond-Blackfan anemia, severe congenital neutropenia, and thrombocytopenia absent radii, single cyto

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10

Goryainova, Nadiya, Stanislav Vydyborets, Yurii Derpak, Olena Kucher, and Halyna Moroz. "Anemic Syndrome and Molecular Mechanisms and Regulation of Iron Absorption in Gastroenterological Diseases." Family medicine. European practices, no. 1 (February 28, 2023): 11–19. http://dx.doi.org/10.30841/2786-720x.1.2023.277472.

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Anemic syndrome is the most often extraintestinal complication in patients with diseases of the digestive tract (DT), which can significantly impair the quality of life. In the literature review, we tried to combine and systematize the accumulated information on the problem of anemic syndrome in DT diseases. Iron-deficiency anemia, chronic disease anemia, B12-deficiency and folio-deficiency anemia are determined depending on the combination of pathogenetic mechanisms. Other variants of anemia are rare. It is necessary to carry out a complex laboratory examination to establish the leading facto

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Goryainova, Nadiya, Stanislav Vydyborets, Yurii Derpak, Olena Kucher, and Halyna Moroz. "Anemic Syndrome and Molecular Mechanisms and Regulation of Iron Absorption in Gastroenterological Diseases." Family Medicine. European Practices, no. 1 (February 28, 2023): 11–19. https://doi.org/10.30841/2786-720X.1.2023.277472.

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Anemic syndrome is the most often extraintestinal complication in patients with diseases of the digestive tract (DT), which can significantly impair the quality of life. In the literature review, we tried to combine and systematize the accumulated information on the problem of anemic syndrome in DT diseases. Iron-deficiency anemia, chronic disease anemia, B12-deficiency and folio-deficiency anemia are determined depending on the combination of pathogenetic mechanisms. Other variants of anemia are rare. It is necessary to carry out a complex laboratory examination to establish the leading facto

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12

Latif, Hina, Nasir Farooq, Rabia Rathore, and Adil Iqbal. "BARDET BIEDL SYNDROME WITH MEGALOBLASTIC ANEMIA." Journal of Akhtar Saeed Medical & Dental College 03, no. 04 (2021): 178–81. https://doi.org/10.51127/jamdcv3i4cr01.

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Bardet Biedl Syndrome (BBS) is a multisystem autosomal recessive rare disorder having variable symptoms ranging from peripheral obesity, retinal degeneration, polydactyly, hypogonadism,and renal impairment among many other features. We present a case of 16 years old female exhibiting characteristic features of Bardet Biedl Syndrome.Key Words: Bardet Biedl syndrome, Obesity,Polydactyly, Hypogonadism

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13

VASILYEVA, L. V., M. I. TALYKOVA, E. V. GOSTEVA, V. I. ZOLOEDOV, L. V. ULYANOVA, and E. YU SUSLOVA. "Influence of anemia on the course of chronic obstructive pulmonary disease." Practical medicine 20, no. 7 (2022): 105–8. http://dx.doi.org/10.32000/2072-1757-2022-7-105-108.

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The study presents the results of examination of 92 patients with chronic obstructive pulmonary disease (COPD) aimed at identifying anemic syndrome. Anemia as a systemic manifestation of the disease was diagnosed in 29% of patients. It was found that in women this syndrome develops significantly more often and at an earlier stage than in men. By the erythrocytes morphology and the degree of iron saturation, anemia was normocytic and hypochromic in most patients. Reliable clinical features of the COPD course in patients with anemic syndrome were identified: anemia significantly worsens the cond

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14

Goryainova, Nadiya, Stanislav Vydyborets, Yurii Derpak, Olena Kucher, and Halyna Moroz. "Anemic Syndrome and Molecular Mechanisms and Regulation of Iron Absorption in Gastroenterological Diseases." Family medicine. European practices, no. 2 (April 28, 2023): 9–17. http://dx.doi.org/10.30841/2786-720x.2.2023.282488.

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In this review, we tried to combine and systematize the accumulated information on the problem of anemic syndrome in the pathologies of the gastrointestinal tract. Anemic syndrome is the most frequent extraintestinal complication in patients with gastrointestinal tract pathology, which can significantly impair the quality of life. Depending on the combination of pathogenitic mechanisms, the iron deficiency, anemia of chronic diseases, B12-deficiency, and folate deficiency anemia are distinguished. Other types of anemia are less common. It is necessary to conduct a comprehensive laboratory exam

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15

Goryainova, Nadiya, Stanislav Vydyborets, Yurii Derpak, Olena Kucher, and Halyna Moroz. "Anemic Syndrome and Molecular Mechanisms and Regulation of Iron Absorption in Gastroenterological Diseases." Family Medicine. European Practices, no. 2 (April 28, 2023): 9–17. https://doi.org/10.30841/2786-720X.2.2023.282488.

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In this review, we tried to combine and systematize the accumulated information on the problem of anemic syndrome in the pathologies of the gastrointestinal tract. Anemic syndrome is the most frequent extraintestinal complication in patients with gastrointestinal tract pathology, which can significantly impair the quality of life. Depending on the combination of pathogenitic mechanisms, the iron deficiency, anemia of chronic diseases, B12-deficiency, and folate deficiency anemia are distinguished. Other types of anemia are less common. It is necessary to conduct a comprehensive laboratory exam

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16

Letnikova, L. I., A. V. Budnevsky, A. A. Natarov, O. S. Saurina, and M. M. Shapovalova. "ASSESSMENT OF NOSOLOGICAL STRUCTURE ASSOCIATED WITH ANEMIC SYNDROME." Problems of Social Hygiene, Public Health and History of Medicine 30, no. 5 (2022): 782–87. http://dx.doi.org/10.32687/0869-866x-2022-30-5-782-787.

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The anemic syndrome at the stage of primary health care delivery on an outpatient basis is a risk factor for an unfavorable outcome in patients with chronic somatic diseases, primarily cardiovascular and oncological pathologies. In order to understand the true prevalence of anemia among outpatients it is necessary to improve the registration of patients with this disease.Aim: to analyze the features of managing patients with anemia in the primary health care system using a computerized patient monitoring system.The study included 1498 patients aged 18 to 80 who were under dispensary observatio

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17

Budnevsky, A. V., A. Yu Simion, and M. M. Shapovalova. "Pathophysiology of anemic syndrome in cardiovascular diseases." NAUKA MOLODYKH (Eruditio Juvenium) 9, no. 2 (2021): 301–12. http://dx.doi.org/10.23888/hmj202192301-312.

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Anemia is a pathology characterized by a decrease in hemoglobin level and, in most cases, in the number of erythrocytes in blood. This concept unites a group of diseases with different etiology, which determines the tactics of management of a patient by a physician or hematologist. According to epidemiological data, today 32.9% of the world population suffer from anemia, which evidences the widespread prevalence of this pathology. Anemia is recognized as an independent risk factor for adverse outcome in cardiovascular diseases, and can be considered not only a predictor, but also a marker of a

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18

Segel, George B. "Anemia." Pediatrics In Review 10, no. 3 (1988): 77–88. http://dx.doi.org/10.1542/pir.10.3.77.

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The differential diagnosis of anemia is made easier by classifying RBC morphology as (1) hypochromic and microcytic, (2) normochromic and normocytic, and (3) macrocytic. This limits the number of diagnostic considerations and, hence, limits the laboratory evaluation. There are relatively few considerations if the RBCs are hypochromic and microcytic, including iron deficiency and the thalassemia syndromes. If the RBCs are normochromic, the reticulocyte percentage indicates whether the bone marrow is providing an appropriate response for the degree of anemia. There also are few possibilities if

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19

Рыбина, О. В., А. В. Губкин, В. Т. Сахин, and О. А. Рукавицын. "Anemic Syndrome in Gastroenterological Diseases: Problems and Solutions." Гематология. Трансфузиология. Восточная Европа, no. 3 (November 10, 2020): 357–71. http://dx.doi.org/10.34883/pi.2020.6.3.022.

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Анемический синдром – наиболее частое внекишечное осложнение у пациентов с патологией желудочно-кишечного тракта (ЖКТ), которое может значимо ухудшить качество жизни. В зависимости от сочетания патогенетических механизмов выделяют железодефицитную, анемию хронических заболеваний, В12-дефицитную и фолиеводефицитную анемию. Другие варианты анемии встречаются реже. Необходимо проведение комплексного лабораторного обследования для установления ведущего фактора в развитии анемии и подбора адекватной терапии. Парентеральные формы препаратов железа и витаминов более предпочтительны для данной категор

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A. Bhat, Rafiq, Saleem A. Wani, and Pankaj Soni. "Plummer-Vinson syndrome: a case report." International Journal of Research in Medical Sciences 6, no. 5 (2018): 1818. http://dx.doi.org/10.18203/2320-6012.ijrms20181785.

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Plummer-Vinson syndrome (PVS) also named as Patterson-Brown-Kelly syndrome is a combined presentation of three things- dysphagia, iron deficiency anemia, and esophageal webs, seen more often in middle aged females. A 30-year-old female presented to us with shortness of breath on exertion and long standing dysphagia and weight loss. After investigations she was found to be severely anemic. Upper GI endoscopy revealed esophageal web. Dilatation of esophageal web was done, anemia was corrected. Patient is on regular follow-up with marked improvement in terms of weight gain and increased functiona

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Prokhorenko, Т. S., A. P. Zima, T. V. Saprina, et al. "SIGNIFICANCE OF INFLAMMATION MARKERS DETERMINED IN PREGNANT WOMEN WITH ANEMIC SYNDROME AND OBESITY." Medical Immunology (Russia) 20, no. 5 (2018): 639–46. http://dx.doi.org/10.15789/1563-0625-2018-5-639-646.

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The purpose of the present study was to specify a role of inflammatory mediators in pathogenesis of various types of anemia in pregnant obese women. We determined IL-1, IL-6, TNFα, C-reactive protein and hepcidin concentrations in blood serum of pregnant women with obesity depending on the type of anemic syndrome, either iron-deficiency anemia, or anemia of chronic diseases. We showed that the content of IL-6 in blood of the obese women exceeds the value of this index in healthy pregnant women (p < 0.05), and it does not depend on the presence and type of anemic syndrome. We found that the

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Zviahina, Oksana V., Sergii V. Shevchuk, Inna P. Kuvikova, and Iuliia S. Segeda. "ANEMIA IN PATIENTS WITH ANKYLOSING SPONDYLITIS, ASSOCIATION WITH THE ACTIVITY OF THE INFLAMMATORY PROCESS AND THE SEVERITY OF THE DISEASE." Wiadomości Lekarskie 73, no. 4 (2020): 715–21. http://dx.doi.org/10.36740/wlek202004117.

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The aim: To estimate the prevalence of anemia in patients with ankylosing spondylitis, major pathogenetic variants and their relationship with the activity of the inflammatory process and the severity of the disease. Materials and methods: 118 patients with ankylosing spondylitis participated in the study, which performed hematologic, biochemical, immunological studies with general haemopoiesis and ferrokinetics parameters, plasma levels of CRP and IL-6. Results: It was found that in Ukrainian population of patients with ankylosing spondylitis, 28.8% of patients has anemic syndrome. The anemia

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Akther, Dr Mantasha. "EVAN’S SYNDROME – A RARE ENTITY." Era's Journal of Medical Research 11, no. 1 (2024): 139–42. http://dx.doi.org/10.24041/ejmr2024.24.

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The Evans syndrome was first identified by Robert Evans in 1951. Primary thrombocytopenic purpura and acquired hemolytic anemia are r e l a t ed by a r a r e autoimmune dis e a s e . Immunologi c a l thrombocytopenia (ITP) and autoimmune hemolytic anemia (AIHA) may develop in this illness simultaneously or consecutively, and immunological neutropenia may also follow ITP. About 2–5% of ITP patients and 5–10% of warm autoimmune hemolytic anemia cases have Evans syndrome, which is often identified by exclusion. Our case report focuses on a female patient, age 15, who complained of anemia, jaundic

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Younas, Alveena, Mohsin Younas, Aamir Ijaz, Zujaja Hina Haroon, and Nida Basharat. "ROGERS SYNDROME-THIAMINE RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME: CASE REPORT." Pakistan Journal of Pathology 33, no. 2 (2022): 69–72. http://dx.doi.org/10.55629/pakjpathol.v33i2.711.

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Thiamine responsive megaloblastic anemia (TRMA) encompasses a complex syndrome of anemia, sensorineural hearing loss and Diabetes Mellitus. We report a 06 years old male child with pallor, bilateral sensorineural hearing loss, Diabetes Mellitus, megaloblastic anemia, retinitis pigmentosa and a normal response to water deprivation test. Child responded well to high doses of thiamine treatment. Rogers Syndrome, a spectrum disease, should be kept in mind in differential diagnosis of Diabetes Mellitus and megaloblastic anemia in population with frequent consanguinity. Thorough medical and family h

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Строгая, Н. В. "Differentiated Approach to the Treatment of Anemic Syndrome in Children with Juvenile Idiopathic Arthritis: Evaluation of Effectiveness." Рецепт 27, no. 2 (2024): 263–73. http://dx.doi.org/10.34883/pi.2024.27.2.012.

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Введение. В настоящее время остается актуальным вопрос коррекции анемического синдрома у детей с ювенильным идиопатическим артритом, который основывается на установлении, а в последующем и устранении причин, ее вызвавших. Цель. Оценка эффективности лечения анемического синдрома у детей с ювенильным идиопатическим артритом на основании дифференцированного подхода с учетом механизма развития анемии. Материалы и методы. Всего был обследован 101 пациент с ювенильным идиопатическим артритом. На основании клинико-лабораторных данных, кроме общего анализа крови и определения ретикулоцитарных индексов

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Alter, Blanche P. "Inherited bone marrow failure syndromes: considerations pre- and posttransplant." Hematology 2017, no. 1 (2017): 88–95. http://dx.doi.org/10.1182/asheducation-2017.1.88.

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Abstract Patients with inherited bone marrow failure syndromes are usually identified when they develop hematologic complications such as severe bone marrow failure, myelodysplastic syndrome, or acute myeloid leukemia. They often have specific birth defects or other physical abnormalities that suggest a syndrome, and sequencing of specific genes or next-generation sequencing can determine or confirm the particular syndrome. The 4 most frequent syndromes are Fanconi anemia, dyskeratosis congenita, Diamond Blackfan anemia, and Shwachman Diamond syndrome. This review discusses the major complicat

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Alter, Blanche P. "Inherited bone marrow failure syndromes: considerations pre- and posttransplant." Blood 130, no. 21 (2017): 2257–64. http://dx.doi.org/10.1182/blood-2017-05-781799.

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Abstract Patients with inherited bone marrow failure syndromes are usually identified when they develop hematologic complications such as severe bone marrow failure, myelodysplastic syndrome, or acute myeloid leukemia. They often have specific birth defects or other physical abnormalities that suggest a syndrome, and sequencing of specific genes or next-generation sequencing can determine or confirm the particular syndrome. The 4 most frequent syndromes are Fanconi anemia, dyskeratosis congenita, Diamond Blackfan anemia, and Shwachman Diamond syndrome. This review discusses the major complicat

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McCullough, Peter A. "Anemia of cardiorenal syndrome." Kidney International Supplements 11, no. 1 (2021): 35–45. http://dx.doi.org/10.1016/j.kisu.2020.12.001.

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Ertunç, Mehmet Emin, Ahmet Genar Çelik, Akif Tahiroğlu, and Ekrem Ünal. "Inherited Bone Marrow Failure Syndromes in Children." Journal of Pediatric Academy 4, no. 1 (2023): 1–5. http://dx.doi.org/10.4274/jpea.2023.218.

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Inherited bone marrow failure syndromes are disorders of hematopoiesis that are mostly encountered in childhood. Taking the basisfrom genetics, they are characterized by pancytopenia, increased risk of developing myelodysplastic syndrome and malignancy.Extrahematopoietic presentations are observed often in addition to symptoms related to defective hematopoiesis (also known asbone marrow failure). The biology, clinical features, and management of the main syndromes such as Fanconi anemia, dyskeratosiscongenita, Shwachman-Diamond syndrome, congenital amegakaryocytic thrombocytopenia, Diamond-Bla

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Tayefi, Maryam, Mahmoud Ebrahimi, Sara Saffar Soflaei, et al. "Prevalence and Risk Factors of Anemia in the MASHAD Cohort Study." Archives of Iranian Medicine 26, no. 6 (2023): 310–15. http://dx.doi.org/10.34172/aim.2023.47.

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Background: Anemia is a serious public health problem which may be associated with cardiovascular diseases (CVDs) and brain damage. This survey aims to determine the prevalence of anemia and its association with demographic and biochemical factors and metabolic syndrome in a human sample derived from the MASHAD cohort study. Methods: This survey was conducted on a sub-sample of 9847 individuals aged 35 to 65 as part of the MASHAD cohort study. Demographic characteristics and biochemical and anthropometrics indices were recorded. Data were analyzed using SPSS version 20. Results: Anemia was see

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Idrissi, Ayoub, Hamza El jadi, Lahoussaine Abainou, et al. "Microcytic Anemia Revealing Acromegaly." Scholars Journal of Medical Case Reports 11, no. 09 (2023): 1753–56. http://dx.doi.org/10.36347/sjmcr.2023.v11i10.008.

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Acromegaly is a rare endocrinopathy, related to the hyperfunction of the somatotropic axis. We report through this observation an unusual mode of discovery of acromegaly: microcytic anemia. 38-year-old patient, followed for 1 year for microcytic anemia under iron treatment. On clinical examination, the patient presents an anemic syndrome with a frank dysmorphic syndrome evoking acromegaly. The assessment showed a microcytic anemia at 3.8 g/dl for which he received a transfusion of 09 red blood cells. An IGF1 assay and a hypothalamic-pituitary MRI confirmed the diagnosis of acromegaly secondary

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Bogdanov, A. N., S. G. Shcherbak, D. Pavlovich, and E. V. Lomonosova. "IRON METABOLISM, IRON DEFICIENCY ANEMIA AND CARDIORENALANEMIA SYNDROME IN IN ELDERLY AND OLD PATIENTS." HERALD of North-Western State Medical University named after I.I. Mechnikov 9, no. 4 (2017): 46–52. http://dx.doi.org/10.17816/mechnikov20179446-52.

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Zahidova, Kamala Kh. "Indexes of the erythropoietin level in the blood plasma of chronic heart failure patients with anemia." Journal of Basic and Clinical Physiology and Pharmacology 29, no. 1 (2018): 11–17. http://dx.doi.org/10.1515/jbcpp-2016-0102.

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AbstractBackground:Anemia aggravates the disease course and the survival rate of chronic heart failure (CHF) patients. The purpose of the study was to investigate the level of erythropoietin (EPO) in CHF patients with anemic syndrome, with the aim to more accurately assess the severity of the disease and its treatment, depending on the anemia degree.Methods:Patients with ischemic CHF of I–IV functional class (FC) with and without anemia were examined (total number of patients=208, patients with anemia=174). The EPO was determined using the enzyme-linked immunosorbent assay. Before treatment, t

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Simonyan, Margarita A., Viktor A. Klochkov, Igor A. Gordeev, et al. "Clinical characteristics and outcomes of anemic patients with coronary artery disease after percutaneous coronary intervention (systematic review)." Saratov Journal of Medical Scientific Research 19, no. 4 (2023): 370–77. http://dx.doi.org/10.15275/ssmj1904370.

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Objective: to explore clinical characteristics and the influence of anemic syndrome on long-term outcomes of patients with coronary artery disease underwent percutaneous coronary intervention (PCI). Review writing methodology. A systematic review was performed according to PRISMA methodology using PubMed, Google Scholar, eLibrary, CyberLeninka databases. Search depth —from 2000 to 2022. The review included 16 original studies. Conclusion. It was shown that the patients with PCI and anemia were older, predominantly male sex as compared with patients without anemic syndrome. The risk of adverse

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Stauder, Reinhard, Peter Valent, and Igor Theurl. "Anemia at older age: etiologies, clinical implications, and management." Blood 131, no. 5 (2018): 505–14. http://dx.doi.org/10.1182/blood-2017-07-746446.

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Abstract Anemia is quite frequently diagnosed in older individuals and is a key indicator of various reactive and clonal conditions. Many underlying diseases, like myelodysplastic syndrome (MDS), develop preferentially in elderly individuals. The prevalence of anemia at older age is increasing, and this is mainly attributable to more frequently applied diagnostics and demographic changes in our societies. The etiology of anemia at older age is complex and ranges from bone marrow failure syndromes to chronic kidney disease, and from nutritional deficiencies to inflammatory processes including i

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Fattizzo, Bruno, Fabio Serpenti, Wilma Barcellini, and Chiara Caprioli. "Hypoplastic Myelodysplastic Syndromes: Just an Overlap Syndrome?" Cancers 13, no. 1 (2021): 132. http://dx.doi.org/10.3390/cancers13010132.

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Myelodysplasias with hypocellular bone marrow (hMDS) represent about 10–15% of MDS and are defined by reduced bone marrow cellularity (i.e., <25% or an inappropriately reduced cellularity for their age in young patients). Their diagnosis is still an object of debate and has not been clearly established in the recent WHO classification. Clinical and morphological overlaps with both normo/hypercellular MDS and aplastic anemia include cytopenias, the presence of marrow hypocellularity and dysplasia, and cytogenetic and molecular alterations. Activation of the immune system against the hematopo

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N, Bhatnagar. "Evan’s Syndrome - A Case Report." Haematology International Journal 4, no. 2 (2020): 1–3. http://dx.doi.org/10.23880/hij-16000174.

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Evan’s syndrome is a rare and chronic autoimmune disease characterised by autoimmune hemolytic anemia and immune thrombocytopenic purpura with a positive Coomb’s test in the absence of an underlying etiology. Majority of the patients with this syndrome have a chronic relapsing course and significant morbidity and mortality despite treatment. We present a case of a 22 year old female, in which, based on the clinical features, Coombs test, hemolytic anemia and thrombocytopenia, a diagnosis of Evans syndrome was made.

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Zviahina, O. V., S. V. Shevchuk, and O. V. Shevchuk. "Prevalence of anemia in patients with ankylosing spondylitis and peculiarities of hemopoiesis and ferrokinetics, depending on the degree of anemia." Reports of Vinnytsia National Medical University 23, no. 2 (2019): 227–33. http://dx.doi.org/10.31393/reports-vnmedical-2019-23(2)-08.

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Anemic syndrome is a frequent complication of ankylosing spondylitis (AS), worsening the course of the disease and prognosis. The purpose of this work was to determine the frequency of anemia, relationship with age, sex and duration of the disease, as well as the peculiarities of hemopoiesis and ferrokinetics in patients with AS. 118 patients with AS and 26 controls were examined. Hematologic parameters were determined on the apparatus of ERMA PCE-210 (Japan), indicators of ferrokinetics were determined on a biochemical analyzer Humalyzer 2000 using sets in accordance with the instructions of

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Borkowski, Joanna, Mojghan Amrikachi, and S. David Hudnall. "Fulminant Parvovirus Infection Following Erythropoietin Treatment in a Patient With Acquired Immunodeficiency Syndrome." Archives of Pathology & Laboratory Medicine 124, no. 3 (2000): 441–45. http://dx.doi.org/10.5858/2000-124-0441-fpifet.

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Abstract We report the case of a 41-year-old black man with acquired immunodeficiency syndrome who developed a severe chronic anemia due to parvovirus infection. Bone marrow biopsy revealed erythroid aplasia. The infectious nature of the anemia was not recognized, and the patient was treated with erythropoietin. The patient's reticulocyte response was inadequate, however, and he remained anemic. A second bone marrow biopsy showed erythroid hyperplasia and prominent intranuclear parvovirus inclusions within erythroid progenitors. Erythropoietin was discontinued and was followed by a course of i

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Shimamura, Akiko. "Inherited Bone Marrow Failure Syndromes: Molecular Features." Hematology 2006, no. 1 (2006): 63–71. http://dx.doi.org/10.1182/asheducation-2006.1.63.

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Abstract Recent advances resulting from the identification of the genes responsible for four inherited marrow failure syndromes, Fanconi anemia, dyskeratosis congenita, Diamond-Blackfan anemia, and Shwachman-Diamond syndrome, are reviewed. The interpretation of genetic testing should be guided by an understanding of the limitations of such testing for each disorder. The possibility of an inherited basis for marrow failure must be considered for adults as well as children with aplastic anemia. Shared molecular themes are emerging from functional studies of the genes underlying the different inh

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Uspenskiy, Yu P., Yu A. Fominykh, K. N. Nadzhafova, and O. I. Veduta. "Pathogenetic mechanisms of anemic syndrome formation in patients with inflammatory bowel diseases." Medical alphabet, no. 20 (August 18, 2021): 29–34. http://dx.doi.org/10.33667/2078-5631-2021-20-29-34.

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Inflammatory bowel diseases are an urgent public health problem and are often complicated by the development of anemic syndrome. Significant progress has been made in the treatment of ulcerative colitis and Crohn's disease, but the correction of associated anemia in most cases remains insufficient. This article describes in detail the pathogenetic mechanisms of the formation of anemic syndrome in inflammatory bowel diseases, as well as possible ways to correct this condition.

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Nikolaienko-Kamyshova, T. P., and E. A. Akhe. "ABOUT CONNECTION AUTOIMMUNE THYROIDITIS WITH MANIFESTATION OF IRON DEFICIENCY ANEMIA IN A CONDITION OF HYPOTHYROIDISM IN GENERAL CLINICAL PRACTICE. CLINICAL CASE." Клінічна та профілактична медицина 3, no. 21 (2022): 62–66. http://dx.doi.org/10.31612/2616-4868.3(21).2022.09.

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Summary: Anemia is a global public health problem that needs to be identified. When determining the algorithms for examination and treatment of anemic syndrome, it is necessary to carefully study the risk factors for its development, taking into account comorbidity. Carrying out of diagnostic search in several directions will allow to specify mechanisms of development of an anemic syndrome which at a combination worsen a clinical condition. Special attention should be paid to patients with manifestations of anemic syndrome on the background of endocrine pathology, namely autoimmune thyro

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Olaosebikan, Rasaq, and Gayle M. Smink. "Severe Anemia and Neutropenia in a Patient with Gollop Wolfgang Syndrome: Implications of Malabsorption-Induced Micronutrient Deficiency. a Case Report." Blood 144, Supplement 1 (2024): 5223. https://doi.org/10.1182/blood-2024-201774.

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Introduction: Gollop-Wolfgang Complex syndrome is a rare congenital limb anomaly characterized by distal bifid femur and tibial agenesis. The etiology of this syndrome is unknown. Copper deficiency, an uncommon cause of severe anemia and cytopenia, results from malabsorption, issues with copper metabolism, or other nutritional deficiencies. Severe anemia and neutropenia due to copper deficiency have been documented in case reports and retrospective studies. Copper is vital for hematopoiesis, particularly in hemoglobin synthesis and red blood cell maturation. We present a case of Gollop-Wolfgan

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Pavliukovych, Nataliia, Oleksandr Pavliukovych, Oleksandr Buriak, Tamara Kopchuk, and Volodymyr Vivsyannuk. "ROLE OF HYPERCORTISOLEMIA IN PROGRESSION OF THE COMORBID COURSE OF CORONARY ARTERY DISEASE, DIABETES MELLITUS TYPE 2 AND ANEMIA." CBU International Conference Proceedings 7 (September 30, 2019): 794–97. http://dx.doi.org/10.12955/cbup.v7.1457.

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INTRODUCTION: Hyperactivation of stress-limiting mechanisms of the organism is a unique physiological response of the human being to chronic hypoxia of different origins. OBJECTIVES: Investigation of dynamics of cortisol synthesis changes in patients with coronary artery disease with comorbid diabetes mellitus type 2 and anemic syndrome in patients of older age groups. METHODS: Blood cortisol level was measured in 40 old and senile coronary artery disease patients with comorbid diabetes mellitus type 2 and anemic syndrome of different degrees of severity. The control group consiste

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Narla, Anupama, and Benjamin L. Ebert. "Ribosomopathies: human disorders of ribosome dysfunction." Blood 115, no. 16 (2010): 3196–205. http://dx.doi.org/10.1182/blood-2009-10-178129.

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Abstract Ribosomopathies compose a collection of disorders in which genetic abnormalities cause impaired ribosome biogenesis and function, resulting in specific clinical phenotypes. Congenital mutations in RPS19 and other genes encoding ribosomal proteins cause Diamond-Blackfan anemia, a disorder characterized by hypoplastic, macrocytic anemia. Mutations in other genes required for normal ribosome biogenesis have been implicated in other rare congenital syndromes, Schwachman-Diamond syndrome, dyskeratosis congenita, cartilage hair hypoplasia, and Treacher Collins syndrome. In addition, the 5q−

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Dimkovic, Sinisa, and Nada Dimkovic. "The cardio-renal anemia syndrome." Medical review 60, no. 7-8 (2007): 357–63. http://dx.doi.org/10.2298/mpns0708357d.

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Introduction. The problem of anemia in congestive heart failure and chronic kidney disease was thought to be insignificant for a long period of time. Recent investigations pointed out that the problem of anemia should be defined in the context of the cardio-renal anemia syndrome. A positive feedback mechanism indicates that cardio-renal anemia syndrome is due to an interaction between congestive heart failure, chronic renal failure and anemia. The aim of the study was to present the possible pathophysiological mechanisms of this syndrome, epidemiological characteristics and therapeutic results

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Spasovski, Dejan, Emilija Sandevska, and Svetlana Krsetvska-Balkanov. "Interrelation between Rheumatic Autoimmune Disease, Autohemolitic Anemia and Cancer Arising as Epiphenomenon on Paraneoplastic Syndrome." International Journal of Clinical Case Reports and Reviews 9, no. 1 (2021): 01–02. http://dx.doi.org/10.31579/2690-4861/169.

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There are hemolytic anemias of different origin. For instance, these states may be induced by means of some exogenic hemolytic factors: by different organic and unorganic hemolytic toxins (phosphorus, phenylhydrazin, saponins, arsenicum, lead and biotoxins – snake venom, mushroom poisons, mycotoxins, etc.), some medical preparations, radiations, some infectious agents and haevy burns. Besides, in some cases, hemolytic anemias are induced by antibodies and immunocompetent cells against own tissues (autoimmune hemolytic anemia).

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Veklich, A. S., and N. A. Koziolova. "Features of acute decompensation of heart failure in patients with type 2 diabetes mellitus with anemia and latent iron deficiency." South Russian Journal of Therapeutic Practice 2, no. 4 (2021): 33–42. http://dx.doi.org/10.21886/2712-8156-2021-2-4-33-42.

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Objective: to assess the contribution of anemia and latent iron deficiency (LID) to the formation of acute decompensation of chronic heart failure (ADHF) in patients with diabetes mellitus (DM) type 2 in history.Materials and methods: a one‑time screening clinical non‑randomized study was conducted. 98 patients with ADHF were examined according to the criteria for inclusion and non‑inclusion, among which 47 (48%) patients suffered from type 2 DM. Among patients with impaired carbohydrate metabolism, 14 (29.8%) patients had an anemic syndrome verified.Results: the prevalence of anemia among hos

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HASHIZUME, Toshihiko. "Good's Syndrome and Pernicious Anemia." Internal Medicine 41, no. 11 (2002): 1062–64. http://dx.doi.org/10.2169/internalmedicine.41.1062.

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Maher, Ossama M., and Hatel R. Moonat. "Fanconi Anemia and Fanconi Syndrome." Journal of Pediatric Hematology/Oncology 38, no. 7 (2016): 585. http://dx.doi.org/10.1097/mph.0000000000000673.

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