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1.
Int J Infect Dis ; 126: 94-97, 2023 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-36427702

RESUMO

INTRODUCTION: Fungal infections of the central nervous system present a variety of clinical syndromes, such as meningitis, encephalitis, raised intracranial pressure with a nonspecific presentation, and, in the last two decades, have increased the incidence of these fungal infections. Fungal meningoencephalitis is frequently associated with Cryptococcus, but this report stands out for presenting one species of Penicillium genus. OBJECTIVES: Here, we present the first case of meningoencephalitis associated with brain injury caused by Penicillium chrysogenum, in a patient who is immunocompetent and was admitted to Hospital Naval Marcílio Dias, Rio de Janeiro, Brazil. METHODS: To identify the fungal species, we performed phenotypic and genotypic methodologies, from the culture to the sequencing of internal transcribed spacer region, and ß-tubulin gene, a rare fungus in cerebrospinal fluid cultures, belonging to the genus Penicillium, was identified. CONCLUSION: We highlight the importance of the first report of meningoencephalitis caused by P. chrysogenum in a patient who is immunocompetent, registered in Brazil. We also emphasize the need for further studies to determine an effective treatment with the least possible side effects for patients infected by fungi that are rarely related to the most severe forms of invasive infections.


Assuntos
Meningite , Meningoencefalite , Micoses , Penicillium chrysogenum , Penicillium , Humanos , Penicillium chrysogenum/genética , Brasil/epidemiologia , Meningoencefalite/diagnóstico , Meningoencefalite/tratamento farmacológico , Penicillium/genética
2.
Artigo em Inglês | MEDLINE | ID: mdl-36383899

RESUMO

Brazilian spotted fever, a zoonotic disease transmitted by ticks, is caused by Rickettsia rickettsii. We report a fulminant case of this zoonosis in a healthy 46-year-old military man in the urban region of Rio de Janeiro city, in October, 2021. Ticks and capybaras (Amblyomma sculptum, Hydrochoerus hydrochaeris, respectively) were identified in the military fields, pointing to the participation of this large synanthropic rodent, recognized as an efficient amplifier host of Rickettsia rickettsii in Brazil. As the military population is considered a risk group for spotted fever, it is necessary to alert health professionals to the importance of the early detection of the disease and its adequate management, mainly in populations that are particularly at risk of exposure to ticks, in order to avoid fatal outcomes.


Assuntos
Militares , Febre Maculosa das Montanhas Rochosas , Carrapatos , Animais , Humanos , Febre Maculosa das Montanhas Rochosas/diagnóstico , Febre Maculosa das Montanhas Rochosas/epidemiologia , Febre Maculosa das Montanhas Rochosas/microbiologia , Brasil/epidemiologia , Rickettsia rickettsii , Roedores , Carrapatos/microbiologia
3.
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1406877

RESUMO

ABSTRACT Brazilian spotted fever, a zoonotic disease transmitted by ticks, is caused by Rickettsia rickettsii. We report a fulminant case of this zoonosis in a healthy 46-year-old military man in the urban region of Rio de Janeiro city, in October, 2021. Ticks and capybaras (Amblyomma sculptum, Hydrochoerus hydrochaeris, respectively) were identified in the military fields, pointing to the participation of this large synanthropic rodent, recognized as an efficient amplifier host of Rickettsia rickettsii in Brazil. As the military population is considered a risk group for spotted fever, it is necessary to alert health professionals to the importance of the early detection of the disease and its adequate management, mainly in populations that are particularly at risk of exposure to ticks, in order to avoid fatal outcomes.

4.
Vet Parasitol ; 271: 38-44, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-31303201

RESUMO

A nucleoside triphosphate diphosphohydrolase-1 (NTPDase 1) was identified on the surface, flagellum and kinetoplast from L. infantum promastigotes by immunocytochemistry and confocal laser scanning microscopy, using immune sera that recognized specifically the B domain of NTPDase 1 and produced against synthetic peptides (LbB1LJ and LbB2LJ) derived from this domain. The polyclonal antibodies had effective antileishmanial effect, reducing significantly in vitro promastigotes growth (21-25%), an antiproliferative effect also demonstrated by immune sera produced against recombinant r-pot B domain, and two other synthetic peptides (potB1LJ and potB2LJ). In addition, using these biomolecules in ELISA technique, IgG1 and IgG2 subclasses reactivities of either healthy dogs or infected by L. infantum and classified clinically as asymptomatic, oligosymptomatic and symptomatic were tested. Analysis of distinct IgG1 and IgG2 seropositivities patterns suggested antibody subclasses binding epitopes along B domain for protection against infection, indicating this domain as a new tool for prophylactic and immunotherapeutic investigations.


Assuntos
Anticorpos Antiprotozoários/imunologia , Doenças do Cão/imunologia , Imunoglobulina G/imunologia , Leishmania infantum/enzimologia , Leishmania infantum/imunologia , Leishmaniose Visceral/veterinária , Nucleosídeo-Trifosfatase/imunologia , Animais , Anticorpos Antiprotozoários/metabolismo , Doenças do Cão/parasitologia , Cães , Leishmaniose Visceral/imunologia , Leishmaniose Visceral/parasitologia , Domínios Proteicos/imunologia
5.
GED gastroenterol. endosc. dig ; 34(4): 173-176, out.-dez. 2015. ilus
Artigo em Português | LILACS | ID: lil-783147

RESUMO

Síndrome LPAC (Low Phospholipid-Associated Cholelithiasis) é uma enfermidade rara, que cursa com manifestações clínicas recorrentes relacionadas à litíase biliar, mesmo após colecistectomia em indivíduos jovens habitualmente com início dos sintomas antes dos 40 anos. Mutações no gene ABCB4 geram baixa concentração de fosfolipídios na secreção biliar, o que favorece a formação de cálculos de colesterol. Seu diagnóstico é estabelecido por critérios clínicos e o tratamento é fundamentado no uso do ácido ursodesoxicólico (UDCA). O objetivo deste artigo é relatar o caso de um paciente com síndrome LPAC.


Achalasia is an uncommon disorder that affects about LPAC syndrome (Low phospholipid-associated cholelithiasis) is a rare illness that leads to recurrent clinical manifestations related to gallstones, even after cholecystectomy in young individuals, usually with onset of symptoms before age 40. Mutations in the gene ABCB4 generate low concentration of phospholipids in bile secretion, which promotes the formation of cholesterol calculations. The diagnosis is established by clinical criteria and treatment is based on the use of ursodeoxycholic acid (UDCA). The objective of this paper is to report the case of a patient with LPAC syndrome.


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Ductos Biliares , Litíase , Síndrome , Ácido Ursodesoxicólico , Colelitíase
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