Luciano de Souza Queiróz

Universidade Estadual de Campinas (UNICAMP)

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Fabiano Reis

Universidade Estadual de Campinas (UNICAMP)

Fábio Rogério

Universidade Estadual de Campinas (UNICAMP)

Anamarli Nucci

Universidade Estadual de Campinas (UNICAMP)

Marcondes C. França

Universidade Estadual de Campinas (UNICAMP)

Fernando Cendes

Universidade Estadual de Campinas (UNICAMP)

Hélder Tedeschi

Universidade Estadual de Campinas (UNICAMP)

J. Lopes de Faria

Universidade Estadual de Campinas (UNICAMP)

Verônica de Araújo Zanardi

Universidade Estadual de Campinas (UNICAMP)

Mateus Dal Fabbro

Universidade Estadual de Campinas (UNICAMP)

Enrico Ghizoni

Universidade Estadual de Campinas (UNICAMP)

Cooperative Institutions

Universidade Estadual de Campinas (UNICAMP)

206

Hospital de Clínicas da Unicamp

105

Universidade de São Paulo

Brazilian Institute of Neuroscience and Neurotechnology

Universidade São Francisco

Universidade Federal de São Paulo

Centro Infantil Boldrini

Pontifícia Universidade Católica de Campinas

Universidade Estadual Paulista (Unesp)

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo

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Seizures and Cerebral Schistosomiasis

Archives of Neurology (2005)

Luiz Eduardo Betting C. L. Pirani Luciano de Souza Queiróz Alfredo Damasceno Fernando Cendes

Background

Schistosoma mansoniis a parasitic trematoid worm that infects humans. Schistosomiasis is endemic in parts of South America, sub-Saharan Africa, the Middle East, and some Caribbean islands. Disorders of the liver and gastrointestinal tract are the most common clinical manifestations. The central nervous system is not usually affected. The most common neurologic manifestation is transverse myelitis. In some circumstances, the eggs ofS mansoniare found in the brain, causing inflammatory reaction.

Objective

To describe a young Brazilian patient with partial epileptic seizures caused by a granulomatous lesion due toS mansoni.

Conclusion

In endemic areas or in patients with a positive epidemiological history, schistosomiasis must be considered as a possible diagnosis of seizures, particularly when they are associated with granulomatous lesions on magnetic resonance imaging.

10.1001/archneur.62.6.1008

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Citations (42)

EGFR, p53, IDH-1 and MDM2 immunohistochemical analysis in glioblastoma: therapeutic and prognostic correlation

Arquivos de Neuro-Psiquiatria (2015)

Richard Murdoch Montgomery Luciano de Souza Queiróz Fábio Rogério

We studied 36 glioblastoma cases at HC-UNICAMP from 2008 to 2012 and classified the immunohistochemical distribution of the wild-type epidermal growth factor receptor (EGFR), mutated forms of p53 protein and isocitrate dehydrogenase-1 (IDH-1) and murine double protein 2 (MDM2). Immunostaining findings were correlated with clinical data and response to treatment (surgery, chemotherapy and radiotherapy). About 97% of the tumors were primary, most of them localized in the frontal lobe. Mean time free of clinical or symptomatic disease and free time of radiological disease were 7.56 and 7.14 months, respectively. We observed a significant positive correlation between expressions of p53 and MDM2, EGFR and MDM2. Clinical, radiological and overall survivals also showed a significant positive correlation. p53 staining and clinical survival showed a significant negative correlation. The current series provides clinical and histopathological data that contribute to knowledge on glioblastoma in Brazilians.

Isocitrate dehydrogenase

Immunostaining

10.1590/0004-282x20150059

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Citations (23)

Lesão na haste hipofisária – Parte II

DOAJ (DOAJ: Directory of Open Access Journals) (2012)

Josie Naomi Iyeyasu Fabiano Reis Luciano de Souza Queiróz Keila Monteiro de Carvalho

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Neuronal ceroid-lipofuscinosis, a type of amaurotic family idiocy: clinical and pathological study of four cases

Arquivos de Neuro-Psiquiatria (1974)

Luciano de Souza Queiróz Joaquim N. da Cruz Neto J. Lopes de Faria

Neuronal ceroid-lipofuscinosis (NCL) is a recent term, proposed for acurate designation of the late-onset types of Amaurotic Family Idiocy (AFI). Histopathology shows ubiquitous intraneuronal accumulation of lipopigments, being the most important factor for characterization of the entity at present time. Biochemical changes and pathogenesis are obscure. NCL is in contrast to the infantile type of AFI (Tay-Sachs disease), in which intraneuronal accumulation of gangliosides (sphingolipids) is due to the well known deficiency of a lysosomal enzyme. The authors report on four cases of NCL, two brothers of the late infantile (Jansky-Bielschowsky) type and a brother and a sister of the juvenile (Spielmeyer-Sjögren) type. One autopsy and three cortical biopsies revealed moderate to severe distention of the neurons by lipopigment, with nerve cell loss, gliosis and cerebral atrophy. Lipopigment was also increased in liver, heart and spleen. The patients were the first in Brazilian literature in whom the storage material was identified as lipopigment by histochemical methods. A brief summary of the clinical features of NCL is presented, and relevant problems are discussed, concerning interpretation of the nature of the storage material, and significance of the disease for gerontological research.

Neuronal ceroid lipofuscinosis

Gliosis

Histopathology

Neuropathology

10.1590/s0004-282x1974000100001

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Citations (3)

Pleomorphic Xanthoastrocytoma: a retrospective study about Magnetic Resonance Imaging findings in a serie of cases with histopathological confirmation in a brazilian university hospital

Vinícius Trindade Gonçalves Fabiano Reis Verônica A. Zanardi Luciano de Souza Queiróz Nelson Marcio Gomes Caserta

Poster: ECR 2011 / C-0164 / Pleomorphic Xanthoastrocytoma: a retrospective study about Magnetic Resonance Imaging findings in a serie of cases with histopathological confirmation in a brazilian university hospital by: Goncalves, F. Reis, V. Zanardi, L. Queiroz, N. M. G. Caserta, T. F. de Souza; Campinas/BR

Pleomorphic xanthoastrocytoma

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Plasmacytoma of head and neck as initial presentation of multiple myeloma

Arquivos de Neuro-Psiquiatria (2011)

Rodrigo Jorge de Oliveira Fabiano Reis Atul K. Taneja Luciano de Souza Queiróz Verônica de Araújo Zanardi

Presentation (obstetrics)

10.1590/s0004-282x2011000100025

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Frontal astrocytoma with metastase to the spinal cord: a case report and review of the literature

J. Jorge Facure Nubor O. Facure Natividade Vieira Luciano de Souza Queiróz Sylvio S. Carvalhal Filho

A case of a right frontal astrocytoma with spinal metastatic lesion in the region of the third dorsal vertebra is reported. The metastatic nodule was removed six months after the craniotomy. In the literature concerning to the dissemination of tumors cells is suggested that there is not a causal relationship between CSF seeding and operative intervention. Acess to the ventricular system or basal cisterns is of primary importance in the production of metastases. Frontal astrocytoma with metastase to the spinal [...]

Cistern

Vertebra

Spinal Cord Neoplasm

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Pain and motor function in patients with inclusion body myositis

Neuromuscular Disorders (2016)

M. Carneiro C. Iwabe-Marchese Júlio S. Martins Carlos Roberto Martins Ingrid Faber

Brief Pain Inventory

Inclusion body myositis

10.1016/j.nmd.2016.06.418

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Giant Cervical Neurofibroma with Concomitant Deformity

JBNC - JORNAL BRASILEIRO DE NEUROCIRURGIA (2018)

Gleidson C. Rodrigues Andrei Fernandes Joaquim Enrico Ghizoni Luciano de Souza Queiróz Hélder Tedeschi

A 27 years-old woman presenting with a giant cervical neurofibroma with spinal cord compression and cervical kyphosis is reported. We discuss the surgical nuances of the multiple surgeries required to achieve a total tumor resection and deformity correction. An algorithm used in our institution to treat cervical kyphosis is also presented.

Kyphosis

Concomitant

Spinal cord compression

10.22290/jbnc.v23i4.1225

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CONGENITAL MYOPATHIES (CNM)

Neuromuscular Disorders (2018)

Tammy Dela Rosa Juliana Almeida Domingues Carlos Roberto Martins Josiel B. Domingos C. Iwabe-Marchese

10.1016/j.nmd.2018.06.176

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