https://repositoriobce.fepecs.edu.br/handle/123456789/1034 2026-02-27T15:22:53Z 2026-02-27T15:22:53Z Bizinoto, Gabriela Parreira Mourão, Ygor Alexandre Lins Faria, Mariana de Gregório Campos, Flávia Gomes de https://repositoriobce.fepecs.edu.br/handle/123456789/1286 2024-08-30T06:00:16Z 2020-12-17T00:00:00Z

Título: Diagnóstico e tratamento da Porfiria Aguda: relato de caso Autor(es): Bizinoto, Gabriela Parreira; Mourão, Ygor Alexandre Lins; Faria, Mariana de Gregório; Campos, Flávia Gomes de Abstract: Objective: Report the clinical condition of a patient admitted at the Hospital Regional de Sobradinho (HRS) with acute intermittent porphyria Case report: Woman, 28 years old, complaining of abdominal pain and acute neurological symptoms, in addition to laboratory tests showing severe hyponatremia and elevated transaminase levels Conclusion: Performing a complete anamnesis, associated with signs, symptoms and laboratory tests, may allow an earlier diagnosis and treatment in order to prevent the evolving to a poor prognosis. Editor: Escola Superior de Ciências da Saúde Tipo: Artigo de Periódico

2020-12-17T00:00:00Z Peixoto, Débora Bernardes Costa Neto, Joaquim Dias da Campos, Flávia Laureto, Jordana Rey Pereira, Talles Borges https://repositoriobce.fepecs.edu.br/handle/123456789/1285 2024-08-30T06:00:21Z 2020-12-17T00:00:00Z

Título: Síndrome neuroléptica maligna: um relato de caso Autor(es): Peixoto, Débora Bernardes; Costa Neto, Joaquim Dias da; Campos, Flávia; Laureto, Jordana Rey; Pereira, Talles Borges Abstract: Introduction: Neuroleptic malignant syndrome is a rare disease, observed mainly in middle-aged men before the 4th decade of life, characterized by fluctuations in the level of consciousness, intense muscle stiffness, dysautonomia (variation in pulse, blood pressure (BP) and respiratory rate) and hyperthermia. The diagnosis is clinical and laboratory, and other causes must be excluded. Description: D.G.S., 43 years old, male, married. He presented with a psychotic outbreak and was medicated with haloperidol and promethazine, subsequently evolving with muscle stiffness, sweating, hyperthermia, neurological changes and elevated creatine phosphokinase (CPK) compatible with the diagnosis of Malignant Neuroleptic Syndrome, probably secondary to haloperidol infusion. Conclusion: The Neuroleptic Malignant Syndrome is characterized by a reaction to the use of neuroleptics and leads the individual to present multiple organ changes, possibly fatal. The diagnosis is clinical and laboratory. The primary treatment is the suspension of the causative drug, and a specific treatment has not yet been established. Editor: Escola Superior de Ciências da Saúde Tipo: Artigo de Periódico

2020-12-17T00:00:00Z Santos, Louise Cristhine de Carvalho Lucas, Phelipe Pinheiro Alves Ferreira, Dilson Palhares https://repositoriobce.fepecs.edu.br/handle/123456789/1253 2024-08-22T06:00:24Z 2021-04-26T00:00:00Z

Título: Nefropatia full-house não relacionada ao lúpus: um relato de caso Autor(es): Santos, Louise Cristhine de Carvalho; Lucas, Phelipe Pinheiro Alves; Ferreira, Dilson Palhares Abstract: Introduction: The systemic lupus erythematosus (SLE) is a chronic multisystemica utoimmune inflammatory disease. Some patients, however, may exhibit a histological pattern of renal injury, with characteristics indistinguishable from lupus nephritis, but without presenting any extra renal symptoms or suggestive SLE serology. Such involvement has recently been called full-house nephropathy unrelated to lupus Description: P.M.G., 19 years old, female, single. She presented endemogenic syndrome associated with hypertension with proteinuria in the nephrotic range and changes in renal function in laboratory tests. It was investigated for the possibility of SLE without filling clinical and laboratory criteria. During hospitalization, she was submitted to renal biopsy with a pattern compatible with full-house nephropathy. She was submitted topulse therapy with Cyclo phosphmide with total recovery of renal function and today she is monitored on the use of corticoid therapy. Conclusions: Full-house nephropathy not related to lupus is a new entity, not yet fully understood the mechanisms of action and therapeutic approach. It still needs further studies and may be the initial manifestation of SLE, isolated manifestation of SLE or a new disease not related to SLE. Editor: Escola Superior de Ciências da Saúde Tipo: Artigo de Periódico

2021-04-26T00:00:00Z Quint, Bruno Beust Amaral, Anamaria de Araújo Falcão Bizinato, Gabriela Parreira Ferreira, Dilson Palhares https://repositoriobce.fepecs.edu.br/handle/123456789/1243 2024-08-17T06:00:19Z 2021-08-24T00:00:00Z

Título: Angioedema hereditário com deficiência de inibidor de C1 esterase e parada cardiorrespiratória: relato de caso Autor(es): Quint, Bruno Beust; Amaral, Anamaria de Araújo Falcão; Bizinato, Gabriela Parreira; Ferreira, Dilson Palhares Abstract: Objective: report the clinical picture of a patient with a previous diagnosis of hereditary angioedema with C1 esterase inhibitor deficiency, associated with cardiorespiratory arrest in an emergency department. Case report: female patient, 23 years old, with previous diagnosis of hereditary angioedema with deficiency of C1 esterase inhibitor, complained of edema on the face and lips, for three days, evolving with sudden worsening and cardiorespiratory arrest. Conclusion: in hereditary angioedema, there may be a sudden, unfavorable worsening, even with cardiorespiratory arrest, which implies early recognition of its potential severity. Clinical improvement could be observed after the use of fresh frozen plasma, performed in an intensive support location. Editor: Escola Superior de Ciências da Saúde Tipo: Artigo de Periódico

2021-08-24T00:00:00Z