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Relevant bibliographies by topics / Generalized edema

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Academic literature on the topic 'Generalized edema'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Generalized edema"

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Ahel, Ivona Butorac, Mirna Šubat Dežulović, and Goran Palčevski. "Generalized edema with hypoproteinemia as initial presentation of celiac disease in a 3-year-old boy: case report." Paediatria Croatica 59, no. 3 (2015): 181–84. http://dx.doi.org/10.13112/pc.573.

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Edema is defined as abnormal accumulation of fluid in the interstitium. Diff erential diagnosis of generalized edema is very broad. Most often, renal and cardiac causes lead to generalized edema. The potential gastrointestinal causes of edema are liver failure and protein losing enteropathy including celiac disease and protein malnutrition. Generalized edema is rarely an initial manifestation of celiac disease. Hereby, we present a case of a 3-year-old boy with celiac disease, initially presented with generalized edema and hypoproteinemia.

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Millichap, J. Gordon. "Juvenile Dermatomyositis with Generalized Edema." Pediatric Neurology Briefs 15, no. 6 (2001): 48. http://dx.doi.org/10.15844/pedneurbriefs-15-6-11.

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Mizell, Joshua, Samar K. Bhowmick, and Rosa A. Vidal. "A Baby With Generalized Edema." Clinical Pediatrics 49, no. 12 (2010): 1157–59. http://dx.doi.org/10.1177/0009922809347778.

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Chandler, Rachel G., Michael J. Wells, Premalatha Vindhya, and Sari Nabulsi. "Generalized edema and erythematous rash." Journal of the American Academy of Dermatology 57, no. 1 (2007): 186–87. http://dx.doi.org/10.1016/j.jaad.2007.04.002.

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Pereira de Godoy, Jose Maria, Henrique Jose Pereira de Godoy, Aline Aparecida de Sene Souza, Ricardo Budtinger Filho, and Maria de Fatima Guerreiro Godoy. "Lipolymphedema Associated with Idiopathic Cyclic Edema: A Therapeutic Approach." Case Reports in Vascular Medicine 2017 (2017): 1–3. http://dx.doi.org/10.1155/2017/5470909.

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Idiopathic cyclic edema is a type of generalized edema that mainly affects women. Diagnosis is made by the patient’s clinical history and an evaluation of the accumulation of weight during the day. The objective of this study is to report the clinical control of lymphedema associated with idiopathic cyclic edema using calcium dobesilate. A 55-year-old female patient reported generalized edema for years in that she woke up in the morning with her legs swollen and the edema worsened during the day. The physical examination revealed generalized edema. After four days of treatment with calcium dob

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Chou, Jen-Wei, Ken-Sheng Cheng, and Ching-Pin Lin. "A Rare Cause of Generalized Edema." Gastroenterology 152, no. 1 (2017): 31–33. http://dx.doi.org/10.1053/j.gastro.2016.08.047.

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Werner de Castro, Gláucio R., Simone Appenzeller, Manoel B. Bértolo, and Lílian T. L. Costallat. "Acute dermatomyositis with subcutaneous generalized edema." Clinical Rheumatology 25, no. 6 (2006): 898–900. http://dx.doi.org/10.1007/s10067-005-0053-9.

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Nishioka, Hiroaki, Tatsuya Shindo, and Hayato Shimizu. "Dermatomyositis Presenting with Generalized Subcutaneous Edema." Internal Medicine 62, no. 15 (2023): 2273–77. http://dx.doi.org/10.2169/internalmedicine.0687-22.

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Irianto and Dewi Catur Wulandari. "Generalized edema on a hypothyroid patient with incorrect use of levothyroxine." International Journal of Advances in Medicine 11, no. 5 (2024): 520–23. http://dx.doi.org/10.18203/2349-3933.ijam20242318.

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Hypothyroidism is manifested when thyroid hormone isn’t enough for body's requirement and is usually diagnosed by high levels of TSH and low levels of fT4. Generalized edema is commonly associated with cardiovascular, hepatic, or renal diseases and is quite uncommon to see in hypothyroidism; the edema is usually generalized when the disease is severe. Generalized edema in hypothyroidism is traditionally accompanied with more serious hypothyroid symptoms, which is not the case here. It is discussed why the other common causes of generalized edema such as heart failure, advanced kidney disease,

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Tuna Kirsaclioglu, Ceyda, Gulin Hizal, Esra Karakus, and Tulin Revide Sayli. "An Unusual Presentation of Cytomegalovirus Infection: Generalized Edema." Medical Principles and Practice 29, no. 1 (2019): 94–96. http://dx.doi.org/10.1159/000500511.

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Objective: Cytomegalovirus (CMV) infection may rarely lead to protein-losing gastropathy that presents with nausea, vomiting, abdominal pain, and edema in immunocompetent children, but extremely rarely with only generalized edema. Clinical Presentation and Intervention: A previously healthy 5-year-old boy presented with generalized edema without any other symptoms. He had hypoalbuminemia but no proteinuria. He was evaluated for gastrointestinal protein loss, and hypertrophic gastropathy was revealed on esophagogastroduodenoscopy. Meanwhile, CMV infection was detected by serologic tests and pol

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Book chapters on the topic "Generalized edema"

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Ghoda, Manoj K. "Case 13: A 6-Month-Old Child with Neonatal Cholestasis and Generalized Edema." In Neonatal and Pediatric Liver and Metabolic Diseases. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-9231-7_14.

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Mandal, Anil. "Generalized Edema (Anasarca)." In Textbook of Nephrology for the Asian-Pacific Physicians. Jaypee Brothers Medical Publishers (P) Ltd., 2004. http://dx.doi.org/10.5005/jp/books/10926_5.

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Coppo, Rosanna, and Claudio Ponticelli. "Minimal change nephropathy." In Treatment of Primary Glomerulonephritis. Oxford University Press, 2009. http://dx.doi.org/10.1093/med/9780199552887.003.0005.

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Minimal change nephropathy (MCN), also called ‘minimal change disease’ in the USA, is chiefly characterized by episodes of nephrotic syndrome—presenting with massive proteinuria, hypoalbuminemia, generalized edema, hyperlipidemia—and no lesions or only minimal glomerular abnormalities in the renal biopsy examined by light microscopy.

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Mandal, Anil. "Generalized Edema (Anasarca): A Systematic Approach to Diagnosis and Management." In Textbook of Nephrology. Jaypee Brothers Medical Publishers (P) Ltd., 2014. http://dx.doi.org/10.5005/jp/books/12351_11.

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Liveson, Jay Allan. "Critical Illness Weakness After Gastric Bypass." In Peripheral Neurology. Oxford University PressNew York, NY, 2000. http://dx.doi.org/10.1093/oso/9780195135633.003.0114.

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Abstract Because of marked obesity, a 28-year-old woman underwent a gastric bypass operation, which was followed by a reoperation for wound problems. In the interim, a nephrotic syndrome was diagnosed when she developed leg edema. She started to develop generalized weakness after the original procedure, progressing during the subsequent days to a severe total quadriparesis. Except for sleep apnea, patient had no prior medical history. Studies revealed atalectatic or fibrotic lung bases, and CT evidence consistent with fatty liver. Serum chemistry abnormalities included total protein, uric acid

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Akarsu, Sevgi, and Fatma Polat. "Possible Cutaneous Adverse Effects of AntiInfective Vaccinations." In Frontiers in Anti-Infective Drug Discovery: Volume 10. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9781681089348124100006.

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Although commonly used anti-infective vaccines in clinical practice are generally safe, certain local or systemic adverse reactions related to them may rarely occur. Actually, considering the general vaccination rates, the incidence of serious skin reactions (e.g . angioedema, anaphylaxis, Stevens–Johnson syndrome) is very low but vaccine-associated local cutaneous reactions such as erythema, edema, tenderness and pain at the injection sites are one of the most common complications of vaccines. Furthermore, a wide variety of specific or non-specific localized or generalized cutaneous adverse e

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Mahboobi, Sohail K., and Ramaiza Sohail. "Burns." In Basic Anesthesia Review, edited by Alaa Abd-Elsayed. Oxford University PressNew York, 2024. http://dx.doi.org/10.1093/med/9780197584569.003.0140.

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Abstract Burns are not uncommon, with approximately 486 000 burn injuries receiving treatment and more than 3000 deaths annually, according to the American Burn Association report. In first few hours, the initial shock phase is followed by generalized edema due to increased capillary permeability, and release of inflammatory substances. Replacement of intravascular volume, to keep perfusing vital organs, should start with balanced salt solutions and with monitoring of urine output, used as an indicator of adequate resuscitation. Certain formulas are used based on body weight and percentage of

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Lyketsos, Constantine G. "Brain Tumors, Systemic Lupus Erythematosus, HIV/AIDS, and Wilson’s Disease." In Psychiatric Aspects of Neurologic Diseases. Oxford University Press, 2008. http://dx.doi.org/10.1093/oso/9780195309430.003.0021.

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This chapter deals with four diseases affecting the central nervous system (CNS) for which neurologists are primarily involved as consultants. It follows the same approach as the chapters that focus on single diseases but does so more briefly. Brain tumors are estimated to have an incidence of 12/100,000 per year (Scharre, 2000). The incidence is highest in old age, peaking between 60 and 80 years of age. Almost 50% of intracranial tumors are gliomas, 10% to 15% are meningiomas, 5% to 7% are pituitary adenomas, and 5% to 6% are metastatic tumors. Brain tumors produce signs and symptoms in a va

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Acierno, Marie D., M. Tariq Bhatti, John J. Chen, and Eric R. Eggenberger. "Fatigue, Blurry Vision, and Swollen Optic Nerves." In Mayo Clinic Cases in Neuroimmunology, edited by Andrew McKeon, B. Mark Keegan, and W. Oliver Tobin. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780197583425.003.0022.

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A 71-year-old woman had development of generalized fatigue over 1 week, along with low-grade fever. The fever resolved, but the fatigue persisted. Subsequently, retro-orbital and head discomfort developed. One month later, she had blurred vision. An ophthalmic examination revealed mild dyschromatopsia, bilateral visual field constriction, bilateral marked optic disc edema, and vitreous cells graded as vitreous haze score 2.0. Magnetic resonance imaging of the brain showed confluent abnormal areas of T2 hyperintensity without mass effect or enhancement involving the subcortical and periventricu

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Nunes, João Matheus Pereira Falcão, Catarina de Jesus Nunes, Giovana da Silva Batista, et al. "ENCEFALITE EQUINA DO LESTE: UMA REVISÃO BIBLIOGRÁFICA DOS ASPECTOS EPIDEMIOLÓGICOS E CLÍNICOS DA DOENÇA." In Open Science Research XIII. Editora Científica Digital, 2023. http://dx.doi.org/10.37885/231014695.

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Introdução: A Encefalite Equina do Leste (EEL) foi diagnosticada inicialmente em Massachusetts, em 1931, nos Estados Unidos da América, descrita como uma arbovirose de alta letalidade e fácil contágio. A doença recebeu esse nome devido ao local na região norte americana que surgiu e sua condição patológica, bem como seu hospedeiro inicial, os equinos, principal alvo do Alphavirus, causador da infecção. Objetivo: Tem-se por objetivo do trabalho avaliar os diversos aspectos em torno da EEL, como epidemiologia, abordagem clínica, diagnóstico e tratamento. Metodologia: A metodologia utilizada foi

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Conference papers on the topic "Generalized edema"

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Namiki, Y., K. Kurasawa, A. Tanaka, et al. "AB0681 Hidden generalized edema in inflammatory myopathy; generalized edema is an unrecognized clinical feature of myositis?" In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.4822.

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Kaur, A., A. S. Dhaliwal, S. Luby, A. Rothman, and J. Salonia. "Negative Pressure Pulmonary Edema Secondary to Generalized Tonic Clonic Seizures." In American Thoracic Society 2022 International Conference, May 13-18, 2022 - San Francisco, CA. American Thoracic Society, 2022. http://dx.doi.org/10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a1436.

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Dunga, Lucas Medeiros, Renner Cassio Nunes de Lucena, Matheus Araújo de Medeiros, et al. "Cerebral tuberculoma as a differential diagnosis for extraaxial lesions in immunocompetent patient: case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.630.

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Introduction: Cerebral tuberculomas are a rare and serious form of tuberculosis, representing 0.2% of intracranial expansive processes. In the absence of conclusive diagnostic tests, doctors often make treatment decisions based on clinical judgment, cerebrospinal fluid (CSF) profile, and radiological findings. Magnetic resonance imaging (MRI) commonly shows discrete lesions with ring enhancement, with perilesional edema, being a relevant differential diagnosis in ring lesions, as their clinical and imaging can mimic brain tumors. The aim to report a case of cerebral tuberculoma in an immunocom

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Xiao, Dua, Raeann Dalton, Adam Fineman, Michael Benz, and Antonios Tsompanidis. "The AngioVac® Device Limits Lethal Complications of Sepsis and Severe Infective Endocarditis with a Large Tricuspid Valve Vegetation: A Case Report." In 27th Annual Rowan-Virtua Research Day. Rowan University Libraries, 2023. https://doi.org/10.31986/issn.2689-0690_rdw.stratford_research_day.55_2023.

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Introduction: Infectious endocarditis of the tricuspid valve is a common complication of intravenous drug use. Endocarditis caused by viridans streptococci can lead to heart valve vegetations which may be life threatening due to the potential for embolism and obstruction. Management of large valvular vegetations is often difficult due to the risks involved with open heart surgery, especially in patients with comorbid conditions. The AngioVac® device has been shown in rare cases to be effective at debulking vegetations without the need for invasive surgery. Case Presentation: We present a patie

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Rocha, Maria Eduarda Araújo Machado da, Andrey Luis de Oliveira Gonçalves Dias, and Nilson Ramirez de Jesus. "Síndrome em espelho associada a síndrome de Beckwith-Wiedemann fetal: um relato de caso." In 45º Congresso da SGORJ XXIV Trocando Ideias. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/jbg-0368-1416-20211311209.

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Introdução: A síndrome em espelho (SE) é uma condição materna rara, definida pela tríade hidropsia fetal, hidropsia placentária e edema materno generalizado. Neste relato, descrevemos um caso de SE associada à síndrome de Beckwith-Wiedemann (SBW), uma anomalia congênita rara. Foi atribuída a expressão “síndrome em espelho” pelo fato de o edema materno refletir o edema fetal. Pode ocorrer em qualquer período da gravidez, mas é mais comum no final do segundo e no início do terceiro trimestre. Está associada a elevada morbimortalidade materna e perinatal. Sua etiopatogenia é variada, e a maioria

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Barros, Jordana Joab Alencar, Alexandre Bravin Moreira, Paulo Roberto Moura de Sousa, Tatiane Oliveira Borges, and Isabela Moreira Dias. "DERMATOMYOSITIS AS PARANEOPLASTIC SYNDROME OF A BREAST CANCER." In XXIV Congresso Brasileiro de Mastologia. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s1021.

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Paraneoplastic syndromes (PS) are entities whose symptoms are not directly attributed to primary or metastatic tumors. They are usually triggered by immunological mechanisms in response to tumor antigens or by hormonal factors. Their appearance may precede, be synchronous, or follow the diagnosis of a neoplasm. Breast cancer can also manifest itself through such syndromes. Dermatomyositis (DM), a rare disease, is an inflammatory myopathy that presents with progressive, symmetrical, proximal muscle weakness, and characteristic cutaneous findings. It is believed that approximately 10%–25% cases

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Barros, Thaís Raylla Laurindo Sena, Julia De Oliveira Silva, Vanessa Saraiva Sousa, Maria José Lima Do Nascimento, and Francisco Lima Silva. "HIDROPSIA FETAL EM NEONATO DE CADELA DA RAÇA ROTTWEILER: RELATO DE CASO." In I Congresso On-line Nacional de Clínica Veterinária de Pequenos Animais. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1832.

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Introdução: A hidropsia fetal é uma alteração caracterizada pelo grande acúmulo de líquido no espaço extravascular, edema de subcutâneo generalizado e nas cavidades peritoneal, pleural e pericárdica. Objetivo: Objetiva-se relatar o nascimento de um filhote canino da raça Rottweiler com hidropsia fetal do tipo anasarca. Materiais e Métodos: Uma cadela da raça Rottweiler, 7 anos e 2 meses, 35 kg foi atendida em caráter emergencial em um hospital veterinário na cidade de Teresina-PI. O tutor relatou que a cadela entrou em trabalho de parto, eliminando apenas três filhotes e secreção purulenta. A

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Oliveira, Luana Desterro e. Silva da Cunha, ADRIANE LINO MIRANDA PINTO, KARLA LINHARES PINTO FARIAS, and RONNEY CORRÊA MENDES. "RELATO DE CASO: ANAFILAXIA CAUSADA POR ÁCAROS." In II Congresso Brasileiro de Imunologia On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/ii-conbrai/6332.

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Introdução: APM, 32, feminino, com prurido generalizado, edema bipalpebral, coriza, espirros e rouquidão repentinos. Hipótese diagnóstica principal: Anafilaxia, que é uma reação alérgica mediada por IgE em superfície de macrófagos e basófilos resultando em sintomas graves. Administrados na emergência adrenalina IM, fluidoterapia, oxigênio, prednisona e anti-histamínicos sistêmicos, com melhora rápida. Doze horas depois recebeu alta com Fexofenadina via oral por 7 dias, evoluindo assintomática. Discorrer acerca da reação alérgica mediada por IgE de hipersensibilidade I gerada por ácaros present

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Silva, Vitória de Freitas Ribeiro da. "CALICIVIROSE SISTÊMICA FELINA: UMA ENFERMIDADE SUBDIAGNOSTICADA." In I Congresso On-line Nacional de Clínica Veterinária de Pequenos Animais. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/1898.

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Introdução: O calicivírus felino, pertencente à família Caliciviridae e gênero Vesivirus, atinge o trato respiratório superior. Devido à alta variabilidade genética, existe uma grande diversidade de cepas, contribuindo para o surgimento de cepas altamente virulentas que infectam, além de células do trato respiratório superior, o fígado, endotélio dos vasos, pâncreas e pulmões, caracterizando uma doença sistêmica. Recentemente, houve o isolamento de cepas de calicivírus associado à doença sistêmica em alguns países da América do Norte, Europa e Ásia. No Brasil ainda não há relatos descritos da

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Magalhães, Maria Regina Marques, and Lorena Moreira Couto. "Descolamento prematuro de placenta: relato de caso." In 46º Congresso da SGORJ e Trocando Ideias XXV. Zeppelini Editorial e Comunicação, 2022. http://dx.doi.org/10.5327/jbg-0368-1416-2022132s1064.

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Introdução: O descolamento prematuro de placenta (DPP) é a separação da placenta normoinserida antes do nascimento do feto. Os principais achados clínicos são sangramento vaginal e dor abdominal, comumente seguidos de contrações uterinas hipertônicas. A grande maioria dos casos acontece antes de 37 semanas, sendo importante causa de prematuridade e morbimortalidade materna e perinatal. A fisiopatologia do DPP pode ser explicada pela ruptura dos vasos maternos na decídua basal. O sangue acumulado atinge a zona de clivagem decíduo-placentária e inicia a separação. Os principais fatores de risco

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