Publications by authors named "Aranha J"

is a relevant zoonotic infectious agent causing swine erysipelas (SE) in wild boar. In Portugal, there is no information on its occurrence. For this reason, this study aims to perform a first serosurvey of SE in hunted wild boars in Portugal.

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Nasopharyngeal myiasis in red deer has never been studied in Portugal. For this reason, from December 2015 to February 2016 a study was derived on hunted red deer in Idanha-a-Nova county to evaluate the Diptera larvae presence. During the initial examination on the spot, the larvae was analysed at the nasopharynx.

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accidentally arrived in Europe (France) in 2004, and rapidly expanded throughout the entire country. Its presence in mainland Portugal was first noticed in 2011. Being an invasive species with no natural predators in the region to control it, it has caused enormous environmental and economic damage, particularly on (honeybee) colonies.

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Article Synopsis
  • Immunosuppressive drugs, crucial for preventing organ rejection in transplant patients, may cause unknown side effects on the brain areas regulating appetite and weight gain.
  • A study on Wistar rats compared the effects of two immunosuppressive treatments (tacrolimus and mycophenolate mofetil) over 14 weeks, observing their impact on hypothalamic nuclei related to food intake.
  • Results indicated that while all rats gained weight, there were no significant changes in neuronal density or morphology in the hypothalamic regions, suggesting that the drugs did not alter these specific brain aspects.
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Since April 2011, Portugal has implemented specific national legislation (Notice No. 1/2011), defining "Epidemiologic Risk Areas for Bovine Tuberculosis in Large Game" and mitigation measures in these areas, including Idanha-a-Nova county. A GIS project was created to record information that would allow us to analyse the spatial-temporal distribution, both for hunting bags and tuberculosis occurrence, in hunted wild boar and red deer in Idanha-a-Nova.

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Pseudoxanthoma elasticum (PXE) is a rare inherited disorder, characterised by a progressive mineralization and fragmentation of elastic fibres of the skin, retina and cardiovascular system. At an initial stage, the skin usually exhibits distinctive lesions and subsequently extra-dermal manifestations. The diagnosis is based on clinical manifestations, histological analysis of the lesions and genetic analysis.

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Objectives: to describe the experience of conducting workshops for teaching the subcutaneous fluid infusion therapy in palliative care patients.

Methods: experience report based on four workshops with a workload of nine hours each, addressing the teaching, implementation of the technique, and management in the use of subcutaneous fluid infusion therapy in patients in palliative care. The host institution was a private hospital, which had two care units in the state of Rio de Janeiro.

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With the increase of forest fires in Portugal in recent decades, a significant part of woodlands is being converted into shrubland areas. : From an ecological point of view, woodlands and shrublands play an essential role, as they not only prevent soil erosion and desertification, but also contribute to soil protection, habitat preservation and restoration, and also increased biodiversity for carbon sequestration. Concerning the shrublands, the assessment of their biomass is essential for evaluating the fuel load and forest fire behavior and also beneficial for obtaining estimates of carbon and biomass for energy use.

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Article Synopsis
  • Multinucleate cell angiohistiocytoma is a rare, benign skin condition characterized by multiple painless red to purple papules, mostly found on the extremities of middle-aged women.
  • * It is likely underdiagnosed because many clinicians and pathologists are not familiar with it.
  • * The text discusses a case of this condition occurring on the face, aiming to raise awareness and highlight its clinical, histopathological, and immunohistochemistry features.
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A 55-year-old man presented with a history of asymptomatic, bilateral, figurate dermatosis consisting of erythematous, annular, linear, andarciform, indurated nodules and plaques on the lateral walls of thorax, flanks, and hypogastrium. His medical history was positive for chronic hepatitis C. Skin biopsy was compatible with the diagnosisof interstitial granulomatous dermatitis.

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Lupus miliaris disseminatus faciei is a rare inflammatory dermatosis of unknown etiology that primarily affects young adults. Clinically, it is characterized by an asymptomatic papular eruption mainly involving the central face, typically on and around the eyelids. Characteristic histopathological features include dermal epithelioid cell granulomas with central necrosis and surrounding lymphocytic infiltrate with multinucleate giant cells.

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Ashy dermatosis is a rare condition, of unknown aetiology, in which mucous membranes are typically spared. The authors report the case of a 57-year-old female with a history of asymptomatic gray-bluish macules located on the trunk and oral mucosa. There were no relief changes on examination.

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A healthy 31-year-old woman presented with a 20-year history of asymptomatic skin-colored papules and nodules on the central area of the face. Her maternal grandmother, aunts, mother, and sister also had similar lesions. Clinical, histopathological, and genetic features allowed the diagnosis of multiple familial trichoepithelioma.

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Introduction: Birt-Hogg-Dubé syndrome (BHDS) is a rare autosomal dominant genodermatosis characterized by cutaneous fibrofolliculomas and/or trichodiscomas, lung cysts, spontaneous pneumothorax and renal tumors. However, its clinical expression is highly variable. This syndrome is caused by germline mutations in the gene () on chromosome 17p11.

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In this study, we characterize the first autochthone case of human sporotrichosis reported in Lisbon, Portugal. Phenotypic and genotypic characterization revealed that the infection was caused by Sporothrix globosa. We conclude that sporotrichosis may be underdiagnosed particularly in Southern Europe and suggest Portugal as an emerging area for this fungal infection.

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We report a case of a 26-year-old Caucasian male presented with 8-month history of asymptomatic erythematous papulonodular lesions symmetrically located on the face, trunk and limbs. Histopathologic examination revealed granulomas with histiocytes arranged in a palisading pattern around the foci of necrobiotic collagen with mucin deposition, and transepidermal and transfollicular elimination of degenerated collagen bundles. These histopathologic findings were compatible with perforating granuloma annulare.

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The overlap syndromes are characterized by the occurrence in the same patient of two or more autoimmune diseases. The overlap syndrome between scleroderma and polymyositis is rare. We describe a case of a 58-year-old woman in which the clinical expression, the effect of therapy and the evolution, support the concept that this syndrome is a distinct clinical entity in the spectrum of autoimmune disease.

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Mycobacterium bovis and, more rarely, Mycobacterium caprae, may cause zoonotic bovine tuberculosis (bTB) in an extensive range of animal species. In Portugal, during 2009, a remarkable raise of bTB incidence was registered in cattle along with an increase of new cases in wildlife. In this work, we reassess and update the molecular epidemiology of bTB in wild ungulates by including 83 new M.

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It has been shown that the activation of cytosolic superoxide dismutase (Sod1) in Saccharomyces cerevisiae is only dependent on Ccs1, which is responsible for insertion of copper into the enzyme catalytic center, and that glutathione (GSH) is not necessary for this process. In this work, we addressed an important role of GSH in Sod1 activation by a Ccs1-dependent mechanism during oxidative stress and its role in yeast lifespan. Exponential cells of Saccharomyces cerevisiae, treated or not with 0.

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Calcification of the mitral annulus is a common echocardiographic finding during routine evaluation of patients. Caseous calcification of the mitral annulus (CCMA) on the other hand is a rare variant, occurring in about 0.06-0.

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