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[PMID]:29465577
[Au] Autor:Peng T; Hu Z; Yang X; Gao Y; Ma C
[Ad] Endereço:Department of Nephrology, Shandong University Qilu Hospital, Jinan City, China.
[Ti] Título:Nitrite-induced acute kidney injury with secondary hyperparathyroidism: Case report and literature review.
[So] Source:Medicine (Baltimore);97(8):e9889, 2018 Feb.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Acute kidney injury (AKI) with hyperparathyroidism caused by nitrite was rare, and renal function and parathyroid hormone (PTH) decreased to normal range after therapy. PATIENT CONCERNS: Acute kidney injury was diagnosed in a 40-year-old male with hyperparathyroidism and cyanosis of his hands and both forearms. DIAGNOSES: The patient ate some recently pickled vegetables, and he experienced nausea, vomiting and diarrhoea without oliguria or anuria; Additionally, his hands and both forearms had a typical blue ash appearance. After admission, the laboratory findings indicated theincreasing serum creatinine (Scr) and parathyroid hormone (PTH). He was diagnosed as acute kidney injury with hyperparathyroidism caused by nitrite. INTERVENTIONS: The patient stopped eating the pickled vegetables and was given rehydration, added calories and other supportive therapy without any glucocorticoids. OUTCOMES: According to his clinical manifestations, laboratory findings and imaging results, the patient was diagnosed with acute kidney injury with secondary hyperparathyroidism. He was given symptomatic supportive care therapy. After one week, the serum creatinine, parathyroid hormone (PTH), hypercalcemia, hyperphosphatemia, proteinuria, and urine red blood cell values decreased to normal range. LESSONS: Nitrite-induced acute kidney injury with secondary hyperparathyroidism was relatively rare. After therapy, the function of the kidney and parathyroid returned to normal. This case suggests that detailed collection of medical history, physical examination and correct symptomatic treatment is very important.
[Mh] Termos MeSH primário: Lesão Renal Aguda/induzido quimicamente
Hiperparatireoidismo Secundário/induzido quimicamente
Nitritos/envenenamento
[Mh] Termos MeSH secundário: Lesão Renal Aguda/terapia
Adulto
Cianose/induzido quimicamente
Diarreia/induzido quimicamente
Hidratação
Conservação de Alimentos
Seres Humanos
Hiperparatireoidismo Secundário/terapia
Masculino
Náusea/induzido quimicamente
Apoio Nutricional
Vômito/induzido quimicamente
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Nm] Nome de substância:
0 (Nitrites)
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180227
[Lr] Data última revisão:
180227
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180222
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009889


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[PMID]:28667718
[Au] Autor:Masavkar SS; Mauskar A; Patwardhan G; Bhat V; Manglani MV
[Ad] Endereço:Department of Pediatrics, Lokmanya Tilak Municipal Medical College and General Hospital, Sion, Mumbai, India. Correspondence to: Dr Sanjeevani Satish Masavkar, Associate Professor, 242/9458, Kannamwar Nagar 2, Vikhroli E, Mumbai 400 083, India. nagotkar.leena@gmail.com.
[Ti] Título:Acquired Methemoglobinemia - A Sporadic Holi Disaster.
[So] Source:Indian Pediatr;54(6):473-475, 2017 Jun 15.
[Is] ISSN:0974-7559
[Cp] País de publicação:India
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: To study clinical profile and outcome in patients with methemoglobinemia following exposure to toxic colors during Holi festival. METHODS: This retrospective study included 112 children (5 to 12 years) admitted with methemoglobinemia after playing Holi. Clinical and treatment details were reviewed. RESULTS: The common symptoms were giddiness, vomiting and headache. Treatment included thorough skin wash, intravenous fluid and methylene blue in 111 children. Age 7-9 and > 11 years, vomiting, giddiness, cyanosis, PaO2 < 80 mm Hg and oxygen saturation < 95% were associated with higher need for methylene blue. All children had a good outcome. CONCLUSION: Timely diagnosis and management of acquired methemoglobinemia can save lives.
[Mh] Termos MeSH primário: Corantes/toxicidade
Férias e Feriados
Metemoglobinemia
[Mh] Termos MeSH secundário: Criança
Pré-Escolar
Cianose
Inibidores Enzimáticos/administração & dosagem
Inibidores Enzimáticos/uso terapêutico
Feminino
Hinduísmo
Seres Humanos
Índia
Masculino
Metemoglobinemia/induzido quimicamente
Metemoglobinemia/diagnóstico
Metemoglobinemia/tratamento farmacológico
Metemoglobinemia/fisiopatologia
Azul de Metileno/administração & dosagem
Azul de Metileno/uso terapêutico
Estudos Retrospectivos
Vômito
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Coloring Agents); 0 (Enzyme Inhibitors); T42P99266K (Methylene Blue)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171017
[Lr] Data última revisão:
171017
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170702
[St] Status:MEDLINE


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[PMID]:28622957
[Au] Autor:Aquino-Andrade A; Martínez-Leyva G; Mérida-Vieyra J; Saltigeral P; Lara A; Domínguez W; García de la Puente S; De Colsa A
[Ad] Endereço:Molecular Microbiology Laboratory, National Institute of Pediatrics, Mexico City, Mexico.
[Ti] Título:Real-Time Polymerase Chain Reaction-Based Detection of Bordetella pertussis in Mexican Infants and Their Contacts: A 3-Year Multicenter Study.
[So] Source:J Pediatr;188:217-223.e1, 2017 Sep.
[Is] ISSN:1097-6833
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: To evaluate the usefulness of real-time polymerase chain reaction (RT-PCR) as a diagnostic method for the detection of Bordetella pertussis in hospitalized patients aged <1 year with a clinical diagnosis of whooping cough, as well as to identify the role of household contacts as a source of infection. STUDY DESIGN: This was a prospective, multicenter study of infants aged <1 year who were hospitalized with symptoms suggestive of whooping cough. Nasopharyngeal samples were obtained for culture and RT-PCR testing. The clinical and epidemiologic characteristics and outcomes were analyzed. B pertussis detection and symptoms in household contacts of patients diagnosed with pertussis were studied. RESULTS: A total of 286 patients were included; of these, 67.1% had B pertussis and 4.5% had Bordetella spp. Complications occurred in 20% of patients, and the mortality rate was 6.7%. Of 434 contacts studied, 111 were mothers of study infants, representing the most frequently B pertussis-infected group and the main symptomatic contact. CONCLUSION: The use of RT-PCR permits improved detection and diagnosis of pertussis and a better understanding of the epidemiology of sources of infection. The complications and mortality rate of pertussis continue to be high. Household contacts are confirmed as a frequent source of infection of B pertussis in young children.
[Mh] Termos MeSH primário: Bordetella pertussis/genética
Reação em Cadeia da Polimerase em Tempo Real
Coqueluche/diagnóstico
Coqueluche/transmissão
[Mh] Termos MeSH secundário: Adolescente
Adulto
Fatores Etários
Contagem de Células
Tosse/etiologia
Cianose/etiologia
DNA Bacteriano/isolamento & purificação
Família
Feminino
Seres Humanos
Lactente
Recém-Nascido
Leucocitose
Masculino
México/epidemiologia
Meia-Idade
Neutrófilos
Pneumonia/epidemiologia
Estudos Prospectivos
Respiração Artificial
Coqueluche/epidemiologia
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE; MULTICENTER STUDY; OBSERVATIONAL STUDY
[Nm] Nome de substância:
0 (DNA, Bacterial)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170911
[Lr] Data última revisão:
170911
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170618
[St] Status:MEDLINE


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[PMID]:28614229
[Au] Autor:Lin TW; Tseng CW; Huang CY; Wang KY; Liang KW
[Ad] Endereço:aCardiovascular Center, Taichung Veterans General Hospital, Taichung bDepartment of Medicine, Cardiovascular Research Center, National Yang Ming University, School of Medicine, Taipei cCishan Hospital, Ministry of Health and Welfare, Kaohsiung dDepartment of Medicine, Chung Shan Medical University eDepartment of Medicine, China Medical University, Taichung, Taiwan.
[Ti] Título:Familial clustering of congenital deafness, patent ductus arteriosus, Eisenmenger complex, and differential cyanosis: A case report.
[So] Source:Medicine (Baltimore);96(24):e7105, 2017 Jun.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Few studies had reported syndromes that include patent ductus arteriosus (PDA) with Eisenmenger syndrome and congenital deafness clustered in male siblings without facial, skeletal, or mental abnormalities. PATIENT CONCERNS: Two brothers, who were deaf and had PDA with Eisenmenger complex, were first seen at our Cardiology clinic at the ages of 25 and 41, respectively. They presented with progressive dyspnea on exertion. Upon physical examination, both brothers had clubbing and/or cyanotic toes, normal fingers, and without facial, skeletal, ophthalmological, or mental abnormalities. DIAGNOSES AND INTERVENTIONS: Echocardiography and multidetector computed tomography revealed large PDAs in both brothers. Cardiac catheterization showed bidirectional shunting via the PDA. OUTCOMES AND LESSONS: Familial clustering of Eisenmenger PDA and congenital deafness is rare. Further studies are warranted to define possible genetic links.
[Mh] Termos MeSH primário: Cianose/complicações
Surdez/complicações
Permeabilidade do Canal Arterial/complicações
Complexo de Eisenmenger/complicações
[Mh] Termos MeSH secundário: Adulto
Cianose/diagnóstico
Cianose/tratamento farmacológico
Surdez/diagnóstico
Surdez/tratamento farmacológico
Diagnóstico Diferencial
Permeabilidade do Canal Arterial/diagnóstico
Permeabilidade do Canal Arterial/tratamento farmacológico
Complexo de Eisenmenger/diagnóstico
Complexo de Eisenmenger/tratamento farmacológico
Seres Humanos
Irmãos
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170717
[Lr] Data última revisão:
170717
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170615
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000007105


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[PMID]:28601176
[Au] Autor:Zucker EJ; Koning JL; Lee EY
[Ad] Endereço:Department of Radiology, Lucile Packard Children's Hospital, Stanford University School of Medicine, 725 Welch Road, Stanford, CA 94305, USA. Electronic address: zucker@post.harvard.edu.
[Ti] Título:Cyanotic Congenital Heart Disease: Essential Primer for the Practicing Radiologist.
[So] Source:Radiol Clin North Am;55(4):693-716, 2017 Jul.
[Is] ISSN:1557-8275
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The cyanotic congenital heart diseases are a rare and heterogeneous group of disorders, often requiring urgent neonatal management. Although echocardiography is the mainstay for imaging, continued technological advances have expanded the role for computed tomography and magnetic resonance imaging, helping to limit invasive cardiac catheterization. In this article, the authors review the broad spectrum of cyanotic congenital heart disease, focusing on the utility of advanced noninvasive imaging modalities while highlighting key clinical features and management considerations.
[Mh] Termos MeSH primário: Cianose/diagnóstico por imagem
Diagnóstico por Imagem/métodos
Cardiopatias Congênitas/diagnóstico por imagem
[Mh] Termos MeSH secundário: Diagnóstico Diferencial
Seres Humanos
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170619
[Lr] Data última revisão:
170619
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170612
[St] Status:MEDLINE


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[PMID]:28501797
[Au] Autor:Egbe AC; Khan AR; Ammash NM; Barbara DW; Oliver WC; Said SM; Akintoye E; Warnes CA; Connolly HM
[Ad] Endereço:Division of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota.
[Ti] Título:Predictors of procedural complications in adult Fontan patients undergoing non-cardiac procedures.
[So] Source:Heart;103(22):1813-1820, 2017 Nov.
[Is] ISSN:1468-201X
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: Limited data exist regarding the outcomes of non-cardiac procedures (NCPs) in adult patients after Fontan operations (Fontan patients). METHODS: To compare procedural outcomes after NCPs in Fontan patients with outcomes for two matched control groups: patients with repaired congenital heart disease and biventricular circulation (CHD-BiV) and patients with no heart disease (NHD). We defined cyanosis as oxygen saturation <90% and procedural hypoxia as saturation <80% or a decrease in saturation >10% from baseline. RESULTS: There were 538 NCPs in 154 Fontan patients (mean age, 30 years) performed in 1990-2015. Sedation and anaesthesia types were monitored anaesthesia care (256,48%), general anaesthesia (51,9%), minimal sedation (105,20%), local anaesthesia (75,14%) and regional anaesthesia (51,9%). Ninety-three complications occurred in 79 procedures (15%) and included arrhythmia requiring intervention (9), hypotension (14), bradycardia (8), hypoxia (38), heart failure requiring intravenous diuretics (2), acute kidney injury (3), bleeding requiring blood transfusion (1), unplanned procedures for dialysis catheter placement (2), readmission (2), unplanned hospitalisation for hypoxia (8) and unplanned transfer to intensive care unit (1). Baseline cyanosis was the only multivariable risk factor for complications (HR, 1.87 (95% CI 1.14 to 3.67), p=0.04). Procedural complications were more common in the Fontan group (18%) than in the CHD-BiV (5%) and NHD groups (1.4%) (p=0.001). CONCLUSIONS: Complications after NCPs were more common in Fontan patients, and baseline cyanosis was a risk factor for complications. All-cause mortality was low and may be related to the multidisciplinary care approach used for Fontan patients at our centre.
[Mh] Termos MeSH primário: Anestesia/métodos
Técnica de Fontan
Cardiopatias Congênitas/cirurgia
Hipnóticos e Sedativos/uso terapêutico
Readmissão do Paciente
[Mh] Termos MeSH secundário: Adulto
Anestesia/efeitos adversos
Anestesia/mortalidade
Cianose/etiologia
Feminino
Técnica de Fontan/efeitos adversos
Técnica de Fontan/mortalidade
Cardiopatias Congênitas/diagnóstico
Cardiopatias Congênitas/mortalidade
Mortalidade Hospitalar
Seres Humanos
Hipnóticos e Sedativos/efeitos adversos
Hipóxia/etiologia
Masculino
Estudos Retrospectivos
Medição de Risco
Fatores de Risco
Fatores de Tempo
Resultado do Tratamento
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Hypnotics and Sedatives)
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171107
[Lr] Data última revisão:
171107
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170515
[St] Status:MEDLINE
[do] DOI:10.1136/heartjnl-2016-311039


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[PMID]:28393795
[Au] Autor:Ladha S; Aggarwal S; Kiran U; Choudhary A; Kapoor PM; Choudhary UK
[Ad] Endereço:Department of Cardiac Anaesthesia, CNC, AIIMS, New Delhi, India.
[Ti] Título:Diagnostic dilemma: Low oxygen saturation during cardiac surgery.
[So] Source:Ann Card Anaesth;20(2):262-264, 2017 Apr-Jun.
[Is] ISSN:0974-5181
[Cp] País de publicação:India
[La] Idioma:eng
[Ab] Resumo:We report a case of rheumatic heart disease with severe mitral stenosis having cyanosis and low oxygen saturation on pulse oximetry. The findings of clinical examination and low values on pulse oximetry were inconsistent with the findings of normal partial pressure of oxygen and oxygen saturation on arterial blood gas analysis, leading to diagnostic dilemma. In such clinical scenario, the anesthesiologist should be aware and vigilant about the differential diagnosis of low oxygen saturation on pulse oximetry.
[Mh] Termos MeSH primário: Cianose/diagnóstico
Implante de Prótese de Valva Cardíaca
Estenose da Valva Mitral/cirurgia
Monitorização Intraoperatória/métodos
Oximetria/métodos
Oxigênio/sangue
[Mh] Termos MeSH secundário: Adulto
Gasometria
Diagnóstico Diferencial
Seres Humanos
Masculino
Valva Mitral/cirurgia
[Pt] Tipo de publicação:CASE REPORTS
[Nm] Nome de substância:
S88TT14065 (Oxygen)
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171102
[Lr] Data última revisão:
171102
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170411
[St] Status:MEDLINE
[do] DOI:10.4103/aca.ACA_34_17


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[PMID]:28393783
[Au] Autor:Bhardwaj V; Malhotra P; Hasija S; Chowdury UK; Pangasa N
[Ad] Endereço:Department of Cardiac Anaesthesia, Cardio Thoracic Centre, All India Institute of Medical Sciences, New Delhi, India.
[Ti] Título:Coagulopathies in cyanotic cardiac patients: An analysis with three point - of - care testing devices (Thromboelastography, rotational thromboelastometry, and sonoclot analyzer).
[So] Source:Ann Card Anaesth;20(2):212-218, 2017 Apr-Jun.
[Is] ISSN:0974-5181
[Cp] País de publicação:India
[La] Idioma:eng
[Ab] Resumo:INTRODUCTION: In the last few years, viscoelastic point-of-care (POC) coagulation devices such as thromboelastography (TEG), rotational thromboelastometry (ROTEM), and Sonoclot (SON) analyzer have been increasingly used in major surgeries for timely assessment and management of coagulopathies. The aim of the present study was to evaluate coagulation profile of cyanotic cardiac patients with TEG, ROTEM, and SON analyzer. In addition, we assessed the correlation of standard laboratory coagulation tests and postoperative chest drain output (CDO) with the parameters of POC testing devices. MATERIALS AND METHODS: Thirty-five patients of either gender, belonging to the American Society of Anesthesiologists Grade I-III, and undergoing elective cardiac surgery on cardiopulmonary bypass for cyanotic congenital heart disease were included in this study. To identify possible coagulation abnormalities, blood samples for TEG, ROTEM, SON, and standard laboratory coagulation were collected after induction of anesthesia. The correlations between variables were assessed using Pearson's correlation coefficient. P < 0.05 was considered statistically significant. RESULTS AND DISCUSSION: EXTEM clot time (CT) and clot formation time (CFT) were prolonged in 87% and 45% patients whereas INTEM CT and CFT were prolonged in 36% and 73% patients, respectively. FIBTEM maximum clot firmness (MCF) was decreased in 30% patients. We observed significant correlation between fibrinogen concentration and ROTEM FIBTEM MCF (r = 0.94, P < 0.001). The SON platelet function (SON PF) showed good correlation with platelet count (r = 0.85, P < 0.001). We also found significant correlation between preoperative FIBTEM MCF and CDO in first 4 postoperative hours (r = 0.49, P = 0.004) and 24 postoperative hours (r = 0.52, P = 0.005). Receiver operating characteristic analysis demonstrated that SON PF and TEG maximum amplitude are highly predictive of thrombocytopenia below 100 × 109/L (area under the curve [AUC] - 0.97 and 0.92, respectively), while FIBTEM-MCF is highly predictive of hypofibrinogenemia (fibrinogen <150 mg/dL (AUC, 0.99). CONCLUSION: Cyanotic cardiac patients have preoperative coagulation abnormalities in ROTEM, TEG, and SON parameters. ROTEM FIBTEM is highly predictive of hypofibrinogenemia while SON PF is highly predictive of thrombocytopenia. ROTEM FIBTEM can be studied as a marker of increased postoperative CDO.
[Mh] Termos MeSH primário: Transtornos da Coagulação Sanguínea/complicações
Transtornos da Coagulação Sanguínea/diagnóstico
Cardiopatias Congênitas/complicações
Cardiopatias Congênitas/cirurgia
Testes Imediatos
Tromboelastografia/métodos
[Mh] Termos MeSH secundário: Testes de Coagulação Sanguínea/métodos
Criança
Cianose
Feminino
Seres Humanos
Masculino
Projetos Piloto
Estudos Prospectivos
[Pt] Tipo de publicação:JOURNAL ARTICLE; OBSERVATIONAL STUDY
[Em] Mês de entrada:1711
[Cu] Atualização por classe:171102
[Lr] Data última revisão:
171102
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170411
[St] Status:MEDLINE
[do] DOI:10.4103/aca.ACA_4_17


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[PMID]:28222032
[Au] Autor:Celmeli F; Kocabas A; Isik IA; Parlak M; Kisand K; Ceylaner S; Turkkahraman D
[Ti] Título:Unexplained cyanosis caused by hepatopulmonary syndrome in a girl with APECED syndrome.
[So] Source:J Pediatr Endocrinol Metab;30(3):365-369, 2017 Mar 01.
[Is] ISSN:2191-0251
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:Autoimmune polyendocrinopathy, candidiasis and ectodermal dystrophy (APECED) is a rare but devastating primary immunodeficiency disease caused by loss-of-function mutations in autoimmune regulator (AIRE) gene on chromosome 21q22.3. The clinical spectrum of the disease is characterized by a wide heterogeneity because of autoimmune reactions toward different endocrine and non-endocrine organs. Here, we report a 17-year-old Turkish girl diagnosed with APECED at 9 years in whom a novel homozygote mutation in AIRE gene p.R15H (c.44G>A) was found. In the clinical course of the patient, chronic liver disease due to autoimmune hepatitis has evolved resulting in hepatopulmonary syndrome (HPS) which has not been reported before in patients with APECED.
[Mh] Termos MeSH primário: Biomarcadores/metabolismo
Cianose/etiologia
Síndrome Hepatopulmonar/complicações
Mutação/genética
Poliendocrinopatias Autoimunes/fisiopatologia
Fatores de Transcrição/genética
[Mh] Termos MeSH secundário: Adolescente
Cianose/patologia
Feminino
Síndrome Hepatopulmonar/genética
Homozigoto
Seres Humanos
Prognóstico
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (APECED protein); 0 (Biomarkers); 0 (Transcription Factors)
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170822
[Lr] Data última revisão:
170822
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170222
[St] Status:MEDLINE


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[PMID]:28167694
[Au] Autor:Agrawal H; Schaefer JD; Teleb M; Cashin LM
[Ad] Endereço:Department of Internal Medicine, Division of Cardiovascular Medicine, Texas Tech University, Paul L Foster School of Medicine, El Paso, Texas, USA.
[Ti] Título:Uncommon cause of adult onset cyanosis: single left ventricle.
[So] Source:BMJ Case Rep;2017, 2017 Feb 06.
[Is] ISSN:1757-790X
[Cp] País de publicação:England
[La] Idioma:eng
[Mh] Termos MeSH primário: Cianose/diagnóstico
Complexo de Eisenmenger/diagnóstico
Cardiopatias Congênitas/etiologia
Hipertrofia Ventricular Esquerda
[Mh] Termos MeSH secundário: Adulto
Complexo de Eisenmenger/diagnóstico por imagem
Cardiopatias Congênitas/diagnóstico
Seres Humanos
Masculino
Artéria Pulmonar/anormalidades
Artéria Pulmonar/diagnóstico por imagem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170321
[Lr] Data última revisão:
170321
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170208
[St] Status:MEDLINE



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