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1.
Rev. bras. ter. intensiva ; 32(3): 474-478, jul.-set. 2020. graf
Article in English, Portuguese | LILACS | ID: biblio-1138507

ABSTRACT

RESUMO Este relato de caso detalha um caso grave de febre amarela complicada por insuficiência hepática e coagulação intravascular disseminada. A tromboelastometria foi capaz de identificar os distúrbios da coagulação e orientar o tratamento hemostático. Relatamos o caso de um homem com 23 anos de idade admitido na unidade de terapia intensiva com quadro com início abrupto de febre e dor muscular generalizada associados a insuficiência hepática e coagulação intravascular disseminada. Os resultados dos exames laboratoriais convencionais revelaram trombocitopenia, enquanto a tromboelastometria sugeriu coagulopatia com discreta hipofibrinogenemia, consumo de fatores de coagulação e, consequentemente, aumento do risco de sangramento. Diferentemente dos exames laboratoriais convencionais, a tromboelastometria identificou o distúrbio de coagulação específico e, assim, orientou o tratamento hemostático. Administraram-se concentrados de fibrinogênio e vitamina K, não sendo necessária a transfusão de qualquer componente do sangue, mesmo na presença de trombocitopenia. A tromboelastometria permitiu a identificação precoce da coagulopatia e ajudou a orientar a terapêutica hemostática. A administração de fármacos hemostáticos, incluindo concentrados de fibrinogênio e vitamina K, melhorou os parâmetros tromboelastométricos, com correção do transtorno da coagulação. Não se realizou transfusão de hemocomponentes, e não ocorreu qualquer sangramento.


Abstract This case report a severe case of yellow fever complicated by liver failure and disseminated intravascular coagulation. Thromboelastometry was capable of identifying clotting disorders and guiding hemostatic therapy. We report the case of a 23-year-old male admitted to the Intensive Care Unit with sudden onset of fever, generalized muscle pain associated with liver failure, and disseminated intravascular coagulation. The results of conventional laboratory tests showed thrombocytopenia, whereas thromboelastometry suggested coagulopathy with slight hypofibrinogenemia, clotting factor consumption, and, consequently, an increased risk of bleeding. Unlike conventional laboratory tests, thromboelastometry identified the specific coagulation disorder and thereby guided hemostatic therapy. Both fibrinogen concentrates and vitamin K were administered, and no blood component transfusion was required, even in the presence of thrombocytopenia. Administration of hemostatic drugs, including fibrinogen concentrate and vitamin K, improved thromboelastometric parameters, correcting the complex coagulation disorder. Blood component transfusion was not performed, and there was no bleeding.


Subject(s)
Humans , Male , Young Adult , Yellow Fever/complications , Blood Coagulation Disorders/diagnosis , Liver Failure/complications , Disseminated Intravascular Coagulation/complications , Thrombelastography/methods , Blood Coagulation Disorders/etiology , Blood Coagulation Disorders/therapy , Hemostatics/administration & dosage , Liver Failure/virology
2.
Rev. Soc. Bras. Med. Trop ; 53: e20200152, 2020. graf
Article in English | SES-SP, ColecionaSUS, LILACS | ID: biblio-1136830

ABSTRACT

Abstract During the yellow fever (YF) outbreak in Brazil, many cases of fulminant hepatitis were seen, although mild to moderate hepatitis was mostly observed with complete recovery. This report presents a case of late-onset hepatitis due to YF relapse. The patient sought medical attention after jaundice recurrence 40 days after the first YF hepatitis episode. This case highlights the importance of patient follow-up after the complete resolution of YF symptoms and discharge.


Subject(s)
Humans , Male , Adult , Yellow Fever/complications , Hepatitis/complications , Recurrence , Hepatitis/immunology
3.
Rev. Soc. Bras. Med. Trop ; 53: e20200141, 2020. tab, graf
Article in English | SES-SP, ColecionaSUS, LILACS | ID: biblio-1136831

ABSTRACT

Abstract INTRODUCTION: Canine visceral leishmaniasis (CVL) is an endemic disease in Brazil, and integrated control actions have been adopted by the Brazilian Ministry of Health to control its spread. However, the transmission profile is unknown in areas with recent CVL cases, including Itaúna, located in the Brazilian state of Minas Gerais, where the present study was carried out. METHODS: A total of 2,302 dogs from 12 neighborhoods were serologically tested for canine VL using the current diagnostic protocol adopted by the Brazilian Ministry of Health. Test positivity rate (TPR) and CVL prevalence were determined for each neighborhood. The presence of Leishmania was assessed in 60 seropositive dogs which had been recommended for euthanasia. Twenty-two of them (37%) were asymptomatic, and 38 (63%) were symptomatic for CVL. Parasitological (myeloculture and smear/imprint) and molecular (PCR) methods were employed for Leishmania detection in bone marrow, spleen, mesenteric lymph nodes, and ear skin. The infecting Leishmania species was identified by DNA sequencing. RESULTS: CVL prevalence (per 1,000 dogs) varied from 0.0-166.67, depending on the neighborhood, with a mean of 68.96 (SD 51.38). Leishmania DNA was detected in at least one tissue from all seropositive dogs, with comparable TPR among tissues. Leishmania parasites were identified in most (54/60) seropositive dogs, and the infecting parasite was identified as Leishmania infantum in all of these. CONCLUSIONS: Prevalence of CVL is a contributor to the spread of visceral leishmaniasis in Itaúna.


Subject(s)
Humans , Male , Adult , Yellow Fever/complications , Hepatitis/complications , Recurrence , Hepatitis/immunology
4.
Autops. Case Rep ; 8(3): e2018038, July-Sept. 2018. ilus
Article in English | LILACS | ID: biblio-911892

ABSTRACT

Disseminated mycosis (DM)­with cardiac involvement and shock­is an unexpected and severe opportunistic infection in patients with yellow fever. DM can mimic bacterial sepsis and should be considered in the differential diagnosis of causes of systemic inflammatory response syndrome in this group of patients, especially in areas where an outbreak of yellow fever is ongoing. We report the case of a 53-year-old male patient who presented to the emergency department with fever, myalgia, headache, and low back pain. The laboratory investigation revealed a positive molecular test for yellow fever, hepatic injury, and renal failure. During hospitalization, the patient developed hepatic encephalopathy, ascending leukocytosis, and ascites, with signs consistent with peritonitis. On the 11th day of hospitalization, the patient developed atrioventricular block, shock and died. At autopsy, angioinvasive mycosis was evidenced mainly in the heart, lungs, kidneys, and adrenals.


Subject(s)
Humans , Male , Middle Aged , Invasive Fungal Infections/complications , Yellow Fever/complications , Autopsy , Diagnosis, Differential , Fatal Outcome , Invasive Fungal Infections/pathology , Kidney/injuries , Renal Insufficiency/complications
6.
Bol. venez. infectol ; 24(1): 39-47, ene.-jun. 2013.
Article in Spanish | LILACS | ID: lil-721091

ABSTRACT

La fiebre amarilla representa a una de las fiebres hemorrágicas que adquieren en Venezuela y a una de las cuatro arbovirosis endémicas que tenemos. Revisando la literatura médica nacional e internacional, se actualizan aspectos relevantes de esta endemia rural. Se mencionan en la etiología las características del agente viral, que tiene ARN como componente primordial de su genoma. En la epidemiología, se menciona su prevalencia en el continente americano y africano y se evalúa su modo de transmisión. En la patogenia y la anatomía patológica se describe al hígado como órgano blanco de la infección. Se destacan en las manifestaciones clínicas los trastornos hemorrágicos y de la coagulación sanguínea. El diagnóstico como en Medicina Tropical, corresponde a un diagnóstico integral: la clínica, en primer lugar, asociada a la epidemiología y a la etiología de la enfermedad. Se establece diagnóstico diferencial con otras entidades relacionadas. El tratamiento es de soporte y en terapia intensiva. Se concluye con la profilaxis, evaluando la utilidad que sigue teniendo la vacunación.


The yelow fever represents one of the hemorrhagic fever that can be acquired in Venezuela and one of the four endemic arbovirosis we have. By reviewing the national and international medical literature. Relevant aspects of this endemic rural disease have been updated. In the etiology, several characterictics of the virus are mentioned; including the RNA as a primordial component of its genome. In the epidemiology, its prevalence on the African and American continents is mentioned, and the transmission mode es evaluated. In the pathogenesis and pathological anatomy, the liver is described as the primary organ of infection. Bleeding and blood clotting disorders are the essential clinical manifestations. Like in Tropical Medicina, The corresponding integral diagnosis is required. In the first instance, the clinical aspects, associated to the epidemiology and to the etiology of the disease are analyzed a diffential diagnosis is made with other related entities. The treatment consists of support measures and Intensive Care in the Intensive Care Unit (ICU). For the prophylaxis, we discuss the advantages of vaccination.


Subject(s)
Humans , Male , Female , Yellow Fever/complications , Yellow Fever/diagnosis , Yellow Fever/epidemiology , Yellow Fever Vaccine/administration & dosage , Communicable Diseases/complications , Communicable Diseases/drug therapy
7.
São Paulo; s.n; 2005. [153] p. ilus, mapas, tab.
Thesis in Portuguese | LILACS | ID: lil-424939

ABSTRACT

Esta análise morfológica e imuno-histoquímica de hepatopatias fulminantes da Amazônia incluindo a série histórica original de Hepatite de Lábrea (HL) e casos de Febre Amarela (FA) concentrou-se em padrões de lesão . Mostraram-se características da FA: morte celular por apoptose medio-zonal, balonização hepatocelular, elevado índice de proliferação celular avaliado pelo PCNA e flebite portal. Os casos de HL mostraram extensa necrose hepatocelular lítica, células “em mórula”, regeneração hepatocelular com multinucleações e transformação pseudo-acinar, flebite portal e centro-lobular, com extinção parenquimatosa, depósitos portais de fibras elásticas e colágeno tipo I e depósitos lobulares de colágeno III / This morphologic and immunohistochemical analysis of fulminant hepatic failure from Amazon Basin, including the original historical series of Labrea Hepatitis (LH) and of Yellow fever (YF) cases was concentrated on lesion patterns. Midzonal apoptotic cellular death, hepatocellular ballooning degeneration, high cellular proliferation index assessed by PCNA and portal phlebitis were shown to be characteristics of YF. LH cases showed extensive lytic hepatocellular necrosis, “morula cells”, hepatocellular regeneration with multinucleation and pseudo-acinar transformation, portal and hepatic vein phlebitis, with parenchymal extinction, portal elastic fibers and type I collagen fibers and lobular type III collagen fiber deposition...


Subject(s)
Infant , Child, Preschool , Child , Adolescent , Adult , Male , Female , Humans , Hemorrhagic Fevers, Viral/diagnosis , Hepatitis D/complications , Liver Diseases/complications , Yellow Fever/complications , Yellow Fever/etiology , Hepatitis D/history
8.
Rev. Soc. Bras. Med. Trop ; 34(1): 83-85, jan.-fev. 2001. ilus
Article in Portuguese | LILACS | ID: lil-462068

ABSTRACT

During an outbreak of yellow fever (rural form of the infection) occurred recently in the State of Goiás, Brazil, a patient, with clinical manifestations suggestive of the infection, died in the University Hospital of Brasilia, DF, on the fifth day from admission. Postmortem examination revealed, microscopically, the characteristic alterations of the infection, and discovered in the lungs and hilar lymph nodes round microrganisms identified as adiaconidia of Emmonsia parva var. crescens.


Durante um surto de febre amarela (forma rural da infecção) instalado, em fins de 1999, no Estado de Goiás, Brasil, um enfermo, com sintomatologia suspeita, faleceu no Hospital Universitário de Brasília, DF, cinco dias após a admissão. À necropsia, microscopicamente, além das alterações hepáticas características da infecção, encontraram-se nos pulmões e linfonodos hilares, estruturas arredondadas, reconhecidas como adiaconídios de Emmonsia parva var. crescens.


Subject(s)
Humans , Male , Middle Aged , Chrysosporium , Yellow Fever/complications , Lung Diseases, Fungal/complications , Fatal Outcome
9.
In. México. Secretaría de Salud. Subsecretaría de Coordinación y Desarrollo. Vacunas, ciencia y salud. México,D.F, Secretaría de Salud, dic. 1992. p.205-15, ilus, mapas.
Monography in Spanish | LILACS | ID: lil-143336

ABSTRACT

Actualmente, la vacuna contra la fiebre amarilla es preparada exclusivamente con la cepa 17D del virus atenuado. Esta vacuna tiene un excelente registro de inocuidad y su poder inmunogénico es elevado. En el pasado se utilizó ampliamente en Africa la cepa "French neurotropic", desarrollada por el Instituto Pasteur de Dakar, a través de múltiples pases en cerebro de ratón. Entre 1940 y 1960 se aplicaron más de 80 millones de dosis por medio de escarificación; sin embargo, se comprobó que la vacuna ocasionaba encefalitis en una proporción pequeña, pero importante, de niños menores de 12 años. Esto dió por resultado que al inicio de la década de los 80 se interrumpiera su producción. Producción mundial de la vacuna: una encuesta realizada en la década de los años ochenta indicó que la producción mundial de la vacuna contra la fiebre amarilla se acercaba a los 19 millones de dosis por año, de las cuales aproximadamente 12 millones fueron producidas por la Fundación Oswaldo Cruz, Brasil. También se estimó que la reserva mundial de la vacuna era de 4.5 millones de dosis, cantidad considerada insuficiente para combatir epidemias extensas, o prevenir la propagación de las mismas a otras áreas. Actualmente hay once laboratorios aprobados por la OMS para la producción de vacunas contra la fiebre amarilla, dos de los cuales están situados en países del Continente Americano


Subject(s)
Mexico , Vaccination/classification , Vaccination/statistics & numerical data , Vaccination/history , Vaccination/instrumentation , Vaccination/methods , Vaccination/trends , Yellow Fever/chemically induced , Yellow Fever/complications , Yellow Fever/diagnosis , Yellow Fever/epidemiology , Yellow Fever/etiology , Yellow Fever/immunology , Yellow Fever/mortality , Yellow Fever/pathology , Yellow Fever/prevention & control
10.
Rev. Inst. Med. Trop. Säo Paulo ; 31(4): 213-20, jul.-ago. 1989. tab
Article in English | LILACS | ID: lil-98007

ABSTRACT

Vinte e quatro casos de hepatite fulminante (HF), internados na Clínica de Doenças Infecciosas e Parasitárias do Hospital das Clínicas da Faculdade de Medicina da Universidade de Säo Paulo durante o período de janeiro de 1976 a dezembro de 1986, foram revistos para a obtençäo de dados clínicos, epidemiológicos e laboratoriais. 88% dos pacientes morreram. Vinte (83%) dos pacientes apresentaram hemorragias, dentre os quais 19 morreram (95%). Infecçöes bacterianas secundárias ocorreram em 14 pacientes (58%) todos os quais faleceram. Ascite foi notada em 3 casos e edema cerebral em 16 casos. Os valores máximos de ALT obtidos para cada paciente durante a internaçäo variaram de 81 a 40460 UI/l. Treze pacientes tiveram elevaçäo de creatinina (54%). A atividade do tempo de protrombina variou de 2,1% a 67%. A febre esteve presente em 20 casos (83%). A encefalopatia surgiu durante as 2 primeiras semanas de doenças em 72% dos casos. Em 7 casos havia doenças associadas à hepatite. A etiologia näo pode ser determinada em 13 casos; 3 casos foram por febre amarela; e 6 casos por outros vírus. Em 1 caso a causa foi drogas e em um caso, possivelmente, foi álcool. Os autores acreditam que a definiçäo de HF merece discussäo antes de ser totalmente aceita. Neste estudo, a HF foi uma doença que acometeu principalmente jovens. A letadade encontrada foi semelhante a de outros estudos. Fatores que contribuiram para o óbito foram hemorragias e infecçöes bacterianas secundárias. Fatores de piora do prognóstico de hepatite foram a presença de outras doenças associadas e de procedimento cirurgico. Os níveis de ALT durante a internaçäo näo refletiram a gravidade da hepatite. Os autores acreditam que a febre amarela deve ser considerada um agente etiológico de HF quando o seu quadro clínico seja compatível com tal, embora os mecanismos fisiopatológicos da encefalopatia sejam ainda obscuros. Os dados clínicos dos 3 casos de febre amarela säo apresentados à parte


Subject(s)
Humans , Male , Female , Infant, Newborn , Infant , Child, Preschool , Child , Adult , Middle Aged , Adolescent , Hepatitis/mortality , Alanine Transaminase/blood , Hepatic Encephalopathy/etiology , Hepatitis/blood , Hepatitis/complications , Hepatitis/etiology , Prognosis , Yellow Fever/complications
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