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Dive into the research topics where Alberto Thomaz Londero is active.

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Featured researches published by Alberto Thomaz Londero.


Revista Da Sociedade Brasileira De Medicina Tropical | 2003

Paracoccidioidomicose: estudo clínico e epidemiológico de 422 casos observados no Estado de Mato Grosso do Sul

Anamaria Mello Miranda Paniago; José Ivan Aguiar; Eliana Setti Albuquerque Aguiar; Rivaldo Venâncio da Cunha; Gracy Regina de Oliveira Leite Pereira; Alberto Thomaz Londero; Bodo Wanke

Clinical and epidemiological features of 422 cases of paracoccidioidomycosis attended at University Hospital of Universidade Federal de Mato Grosso do Sul (Campo Grande, Mato Grosso do Sul, Brazil) from January 1980 to August 1999, were analysed. The mean age was 43.4 years old and the male: female ratio was 10:1. Nearly half (45.5%) of the patients were agricultural workers at the moment of diagnosis. In the acute/subacute form (juvenile type) the phagocytic-monocytic system was very much impaired and mainly marked by lymphadenopathy (95.4%), hepatomegaly (40%), splenomegaly (23.1%). The chronic form (adult type) presents more lesions in oropharynx (66.4%), dysphonia (31.4%) and cough (50.7%). Mycological diagnosis was obtained by direct microscopy of wet mounts in 185/365 (50.7%) patients and by histopathological examination of biopsies in 294/302 (97.3%) patients. The treatment of choice was Sulfamethoxazole/ trimethoprim (Co-trimoxazole), used in 90.3% patients. Sequelae occurred in 30.3% and death in 7.6% of the cases.


Revista Do Instituto De Medicina Tropical De Sao Paulo | 2001

Histoplasmosis in Rio Grande do Sul, Brazil: a 21-year experience

Luiz Carlos Severo; Flávio de Mattos Oliveira; Klaus Loureiro Irion; Nelson da Silva Porto; Alberto Thomaz Londero

Of 156 cases of histoplasmosis observed in the State of Rio Grande do Sul (Brazil), during a 21-year period (1978-1999) 137 were included in this study. Sixty-seven per cent of the patients had hematogeneous disseminated histoplasmosis, 24% had a self-limited syndrome (acute pulmonary histoplasmosis, histoplasmoma or primary pulmonary lymph node complex), and 9 per cent had chronic pulmonary histoplasmosis. Clinical, mycological, and epidemiological data were reviewed and commented.


Mycopathologia | 1979

Occurrence of subcutaneous zygomycosis caused by Basidiobolus haptosporus in Brazil

Achiléa L. Bittencourt; Alberto Thomaz Londero; Maria das Graças Santana Araujo; Núbia Mendonça; Jorge Luiz Andrade Bastos

There were described the first three South American cases of subcutaneous zygomycosis caused by B. haptosporus. The patients were children from nearby towns lying just north of 13 ° latitude S. The diagnosis was based on histopathological aspects plus cultural isolation of the fungus.


Mycopathologia | 1981

The gamut of progressive pulmonary paracoccidioidomycosis

Alberto Thomaz Londero; L. C. Severo

Paracoccidioidomycosis is an important Latin American endemy. The lung is the portal of entrance of the infection and the lesions are confined to this organ in, at least, 30 per cent of the progressive cases. Twelve case histories of patients with the progressive pulmonary form are presented in order to illustrate the repetitious clinical manifestations but the large variety of radiological presentations. The mycologic diagnosis is also emphasized.


Mycopathologia | 1978

The status of histoplasmosis in Brazil.

Alberto Thomaz Londero; Ceci D. Ramos

Thirty four cases of the progressive form of histoplasmosis, five epidemics of the mycosis, many histoplasmin skin test surveys and few clinical or histological evidences of the benign form of the disease were reported in Brazil. The occurrence of the infection in animals and the isolation ofH. capsulatum from soil have also been reported.


Medical Mycology | 1997

Cerebral phaeohyphomycosis caused by Cladophialophora bantiana in a Brazilian drug abuser

R. Walz; M. Bianchin; M.L. Chaves; M.R. Cerski; L.C. Severo; Alberto Thomaz Londero

We present a case of cerebral phaeohyphomycosis caused by Cladophialophora bantiana in an apparently immunocompetent patient with a history of intravenous drug use. The diagnosis was achieved in specimens obtained at necropsy by histological and mycological examination, with subsequent identification of the isolate in culture.


Mycopathologia | 1981

Pulmonary paracoccidioidomycosis in a nine year old girl

Cecy D. Ramos; Alberto Thomaz Londero; Maria C. L. Gal

A case of pulmonary paracoccidioidomycosis in a nine year old girl is reported. This is the first proven case of exclusive pulmonary paracoccidioidal lesions observed in a child. A review of the mycosis among children 0 to 10 years old is also presented.


Mycopathologia | 1978

Progressive pulmonary paracoccidioidomycosis a study of 34 cases observed in Rio Grande do Sul (Brazil).

Alberto Thomaz Londero; Cecy D. Ramos; J. O. Lopes

Data on 34 patients with progressive pulmonary paracoccidioi domycosis seen in the State of Rio Grande do Sul (Brazil) are reviewed. Clinical manifestations were similar to those of a prolonged or a recurrent undifferentiated respiratory infection. Roentgenographic findings were also non-characteristic. A mycologic diagnosis was readily made when sputum was available.


Revista Do Instituto De Medicina Tropical De Sao Paulo | 2002

The spectrum of computerized tomography (CT) findings in central nervous system (CNS) infection due to Cryptococcus neoformans var. gattii in immunocompetent children

Maria do Perpétuo Socorro Costa Corrêa; Luiz Carlos Severo; Flávio de Mattos Oliveira; Klaus Loureiro Irion; Alberto Thomaz Londero

Cranial CT scans of eleven immunocompetent children with central nervous system (CNS) infection due to Cryptococcus neoformans var. gattii were retrospectively reviewed. These children had an average age of 8.8 years and positive culture for C. n. var. gattii in cerebrospinal fluid. The most common signs and symptoms were headache, fever, nuchal rigidity, nausea and vomiting. No normal cranial CT was detected in any patient. Hypodense nodules were observed in all patients. The remaining scan abnormalities were as follows: nine had diffuse atrophy, six had hydrocephalus, and five had hydrocephalus coexistent with diffuse atrophy.


Journal of The American Academy of Dermatology | 1993

Dermatophilus congolensis human infection

Loan Towersey; Eunice de Castro Soares Martins; Alberto Thomaz Londero; Roderick J. Hay; Porphirio José Soares Filho; Cristina Maeda Takiya; Cláudio César Martins; Olga Fischman Gompertz

Four cases of human dermatophilosis observed in Rio de Janeiro, Brazil, are reported. Data that suggest nail infection by Dermatophilus congolensis are presented. The clinical spectrum of the disease ranged from an asymptomatic infection to a pustular eruption. Our findings suggest that epidermal Langerhans cells play a role in the pathogenesis of the infection.

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Cecy D. Ramos

Universidade Federal de Santa Maria

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Luiz Carlos Severo

Universidade Federal do Rio Grande do Sul

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Olga Fischman

Federal University of São Paulo

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Bodo Wanke

Oswaldo Cruz Foundation

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Flávio de Mattos Oliveira

Universidade Federal do Rio Grande do Sul

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Glaura Martha Florim Terra

Federal University of Rio de Janeiro

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Susie Andries Nogueira

Federal University of Rio de Janeiro

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Loan Towersey

Federal University of Rio de Janeiro

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