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Detalle del título uniforme
Radiology Case Reports
Tipo de obra :
Autre
Naturaleza de la obra :
Oeuvre
|
Documentos disponibles con este título uniforme (9)
Clasificado(s) por (Año de edición descendente) Refinar búsquedaMalignant peripheral nerve sheath tumor in a child / Lina Marcela Cadavid Álvarez ; Gabriel Jaime Varela Aguirre
Título : Malignant peripheral nerve sheath tumor in a child Tipo de documento : documento electrónico Autores : Lina Marcela Cadavid Álvarez, ; Gabriel Jaime Varela Aguirre, Fecha de publicación : 2021 Títulos uniformes : Radiology Case Reports Idioma : Inglés (eng) Palabras clave : Child Malignant peripheral nerve sheath tumor Nerve sheath neoplasms Neurofibroma Peripheral nerve Schwannoma Resumen : Among the diverse causes of posterior mediastinal masses, malignant peripheral nerve sheath tumors is a very rare neurogenic tumor. Imaging features tend to be variable. A 20-month-old toddler presented with a 3-month history of persistent diffuse thoracic and abdominal pain. A chest magnetic resonance imaging was taken and shown a posterior mediastinal lesion. Histopathology and immunohistochemical analysis confirmed the diagnosis of a malignant peripheral nerve sheath tumor with myxoid areas. Malignant peripheral nerve sheath tumors are an uncommon entity in the children with a poor prognosis. Magnetic resonance imaging is the preferred technique in children to limit the use of ionizing radiation and because has a higher contrast resolution; however, all suspicious tumors should be biopsied to make an appropriate diagnosis. Treatment is radical surgery with excision of the entire mass; however, there is a high incidence of local recurrence. Mención de responsabilidad : Brian Daniel Noreña-Rengifo MD, Lina Marcela Cadavid-Alvarez RR, Patricia Eugenia Gil-Serrano RR y Gabriel Jaime Varela-Aguirre PR Referencia : Radiol Case Rep. 2020 Nov 12;16(1):145-151. DOI (Digital Object Identifier) : 10.1016/j.radcr.2020.10.028 PMID : 33224401 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930-0433(20)30547-1 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5750 Malignant peripheral nerve sheath tumor in a child [documento electrónico] / Lina Marcela Cadavid Álvarez, ; Gabriel Jaime Varela Aguirre, . - 2021.
Obra : Radiology Case Reports
Idioma : Inglés (eng)
Palabras clave : Child Malignant peripheral nerve sheath tumor Nerve sheath neoplasms Neurofibroma Peripheral nerve Schwannoma Resumen : Among the diverse causes of posterior mediastinal masses, malignant peripheral nerve sheath tumors is a very rare neurogenic tumor. Imaging features tend to be variable. A 20-month-old toddler presented with a 3-month history of persistent diffuse thoracic and abdominal pain. A chest magnetic resonance imaging was taken and shown a posterior mediastinal lesion. Histopathology and immunohistochemical analysis confirmed the diagnosis of a malignant peripheral nerve sheath tumor with myxoid areas. Malignant peripheral nerve sheath tumors are an uncommon entity in the children with a poor prognosis. Magnetic resonance imaging is the preferred technique in children to limit the use of ionizing radiation and because has a higher contrast resolution; however, all suspicious tumors should be biopsied to make an appropriate diagnosis. Treatment is radical surgery with excision of the entire mass; however, there is a high incidence of local recurrence. Mención de responsabilidad : Brian Daniel Noreña-Rengifo MD, Lina Marcela Cadavid-Alvarez RR, Patricia Eugenia Gil-Serrano RR y Gabriel Jaime Varela-Aguirre PR Referencia : Radiol Case Rep. 2020 Nov 12;16(1):145-151. DOI (Digital Object Identifier) : 10.1016/j.radcr.2020.10.028 PMID : 33224401 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930-0433(20)30547-1 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5750 Reserva
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Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD001645 AC-2021-001 Archivo digital Producción Científica Artículos científicos Disponible Documentos electrónicos
2021-001Adobe Acrobat PDF
Título : Primitive neuroectodermal tumor of the liver: a case report of a rare case in pediatrics Tipo de documento : documento electrónico Autores : Lina Marcela Cadavid Álvarez, ; Jorge Alberto Ochoa Gaviria, ; Juan Camilo Pérez Cadavid, Fecha de publicación : 2021 Títulos uniformes : Radiology Case Reports Idioma : Inglés (eng) Palabras clave : Primitive neuroectodermal tumor Focal hepatic lesion Ewing sarcoma Resumen : Primitive neuroectodermal tumors (PNETs) belong to the Ewing sarcoma family of tumors. These lesions are highly aggressive and are usually found in paravertebral regions, lower limbs, and thorax. However, abdominal PNETs are extremely rare, and only 3 cases of pediatric PNET of the liver have been previously reported. Most patients exhibit symptoms associated with mass effect, due to rapid tumor growth and dissemination. Therefore, an appropriate differential diagnosis is of pivotal importance in order to initiate the corresponding treatment. Here we report the case of a 4-year-old female patient who was diagnosed with PNET of the liver, and we discuss the analysis of focal liver lesions and differential diagnosis in pediatric patients. Mención de responsabilidad : Juan David Vásquez Montoya, Lina Marcela Cadavid Álvarez, Jorge Alberto Ochoa Gaviria, Juan Camilo Pérez Cadavid Referencia : Radiol Case Rep. 2021 Jun 13;16(8):2220-2225. DOI (Digital Object Identifier) : 10.1016/j.radcr.2021.05.001 PMID : 34178196 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930043321002909 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5803 Primitive neuroectodermal tumor of the liver: a case report of a rare case in pediatrics [documento electrónico] / Lina Marcela Cadavid Álvarez, ; Jorge Alberto Ochoa Gaviria, ; Juan Camilo Pérez Cadavid, . - 2021.
Obra : Radiology Case Reports
Idioma : Inglés (eng)
Palabras clave : Primitive neuroectodermal tumor Focal hepatic lesion Ewing sarcoma Resumen : Primitive neuroectodermal tumors (PNETs) belong to the Ewing sarcoma family of tumors. These lesions are highly aggressive and are usually found in paravertebral regions, lower limbs, and thorax. However, abdominal PNETs are extremely rare, and only 3 cases of pediatric PNET of the liver have been previously reported. Most patients exhibit symptoms associated with mass effect, due to rapid tumor growth and dissemination. Therefore, an appropriate differential diagnosis is of pivotal importance in order to initiate the corresponding treatment. Here we report the case of a 4-year-old female patient who was diagnosed with PNET of the liver, and we discuss the analysis of focal liver lesions and differential diagnosis in pediatric patients. Mención de responsabilidad : Juan David Vásquez Montoya, Lina Marcela Cadavid Álvarez, Jorge Alberto Ochoa Gaviria, Juan Camilo Pérez Cadavid Referencia : Radiol Case Rep. 2021 Jun 13;16(8):2220-2225. DOI (Digital Object Identifier) : 10.1016/j.radcr.2021.05.001 PMID : 34178196 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930043321002909 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5803 Reserva
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Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD001734 AC-2021-053 Archivo digital Producción Científica Artículos científicos Disponible Documentos electrónicos
2021-053Adobe Acrobat PDF
Título : Thrombosis in abdominal vessels associated with COVID-19 Infection: A report of three cases Tipo de documento : documento electrónico Autores : Santiago Echeverri Isaza, Fecha de publicación : 2021 Títulos uniformes : Radiology Case Reports Idioma : Inglés (eng) Palabras clave : COVID- 19 thrombosis complications mesenteric ischemia computed tomography Resumen : Hypercoagulability related to SARS-CoV-2 infection is one of the main extrapulmonary complications of COVID-19. We present three cases of intrabdominal thrombotic complications related to the state of hypercoagulability of COVID-19 and its tomographic features. Hypercoagulability state should be taking into account in the interpretation of radiological images in all infected patients with COVID-19. Mención de responsabilidad : Ana María Posada-Arango M.D., Joaquín García-Madrigal M.D., Santiago Echeverri-Isaza M.D., German Alberto-Castrillón M.D., David Martínez M.D., Andrea C. Gómez BS, Joseph A. Pinto Msc and Luis Pinillos M.D. Referencia : Radiol Case Rep. 2021 Oct;16(10):3044-3050. DOI (Digital Object Identifier) : 10.1016/j.radcr.2021.07.032 PMID : 34306276 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930043321004969 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5851 Thrombosis in abdominal vessels associated with COVID-19 Infection: A report of three cases [documento electrónico] / Santiago Echeverri Isaza, . - 2021.
Obra : Radiology Case Reports
Idioma : Inglés (eng)
Palabras clave : COVID- 19 thrombosis complications mesenteric ischemia computed tomography Resumen : Hypercoagulability related to SARS-CoV-2 infection is one of the main extrapulmonary complications of COVID-19. We present three cases of intrabdominal thrombotic complications related to the state of hypercoagulability of COVID-19 and its tomographic features. Hypercoagulability state should be taking into account in the interpretation of radiological images in all infected patients with COVID-19. Mención de responsabilidad : Ana María Posada-Arango M.D., Joaquín García-Madrigal M.D., Santiago Echeverri-Isaza M.D., German Alberto-Castrillón M.D., David Martínez M.D., Andrea C. Gómez BS, Joseph A. Pinto Msc and Luis Pinillos M.D. Referencia : Radiol Case Rep. 2021 Oct;16(10):3044-3050. DOI (Digital Object Identifier) : 10.1016/j.radcr.2021.07.032 PMID : 34306276 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930043321004969 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5851 Reserva
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Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD001789 AC-2021-101 Archivo digital Producción Científica Artículos científicos Disponible Documentos electrónicos
2021-101Adobe Acrobat PDF
Título : Giant forehead plasmacytoma as a growing lump in a patient with multiple myeloma Tipo de documento : documento electrónico Autores : Yoel Korenfeld Kaplan, ; Ricardo Andrés Cardona Quiceno, Fecha de publicación : 2020 Títulos uniformes : Radiology Case Reports Idioma : Inglés (eng) Palabras clave : Multiple myeloma Plasmacytoma Forehead Neoplasms Plasma cell Resumen : Extramedullary plasmacytoma represents less than 5% of plasma cell malignancies, 85% corresponding to head and neck masses. Symptoms are related to compressive effects according to location, aesthetics issues and can be misleading associated with soft tissue disorders. In this case report, we discuss a 70-year-old woman who presented with a 3-month history of a growing painless forehead lump and confusion, for which she had an emergent simple head computed tomography scan. The images revealed a well-defined mass eroding the frontal bone with multiple lytic lesions that were also found along with long bones radiography. The mass biopsy showed a monomorphic plasmatic cell infiltrate, bone marrow studies confirmed the diagnosis of a light chain secreting multiple myeloma. Extramedullary plasmacytoma is a very unusual first presentation form of multiple myeloma and represents a clinical and radiological challenge. A systematic approach of lytic bone lesions along with the differential diagnosis of head masses are skills the clinician should develop to promptly recognize this condition considering further complications of delayed treatment. In this case, the histopathological confirmation allowed the patient to avoid neurosurgery and the early start of systemic chemotherapeutic treatment. Mención de responsabilidad : Adriana M Trejos T, María C Cuartas M, Yoel Korenfeld K y Ricardo Cardona Q Referencia : Radiol Case Rep. 2020 Oct 9;15(12):2589-2593. DOI (Digital Object Identifier) : 10.1016/j.radcr.2020.09.050 PMID : 33082903 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930-0433(20)30509-4 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5186 Giant forehead plasmacytoma as a growing lump in a patient with multiple myeloma [documento electrónico] / Yoel Korenfeld Kaplan, ; Ricardo Andrés Cardona Quiceno, . - 2020.
Obra : Radiology Case Reports
Idioma : Inglés (eng)
Palabras clave : Multiple myeloma Plasmacytoma Forehead Neoplasms Plasma cell Resumen : Extramedullary plasmacytoma represents less than 5% of plasma cell malignancies, 85% corresponding to head and neck masses. Symptoms are related to compressive effects according to location, aesthetics issues and can be misleading associated with soft tissue disorders. In this case report, we discuss a 70-year-old woman who presented with a 3-month history of a growing painless forehead lump and confusion, for which she had an emergent simple head computed tomography scan. The images revealed a well-defined mass eroding the frontal bone with multiple lytic lesions that were also found along with long bones radiography. The mass biopsy showed a monomorphic plasmatic cell infiltrate, bone marrow studies confirmed the diagnosis of a light chain secreting multiple myeloma. Extramedullary plasmacytoma is a very unusual first presentation form of multiple myeloma and represents a clinical and radiological challenge. A systematic approach of lytic bone lesions along with the differential diagnosis of head masses are skills the clinician should develop to promptly recognize this condition considering further complications of delayed treatment. In this case, the histopathological confirmation allowed the patient to avoid neurosurgery and the early start of systemic chemotherapeutic treatment. Mención de responsabilidad : Adriana M Trejos T, María C Cuartas M, Yoel Korenfeld K y Ricardo Cardona Q Referencia : Radiol Case Rep. 2020 Oct 9;15(12):2589-2593. DOI (Digital Object Identifier) : 10.1016/j.radcr.2020.09.050 PMID : 33082903 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930-0433(20)30509-4 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5186 Reserva
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Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD001632 AC-2020-126 Archivo digital Producción Científica Artículos científicos Disponible Documentos electrónicos
2020-126.pdfAdobe Acrobat PDF
Título : Breast hemangioma in a male patient: Report of a case Tipo de documento : documento electrónico Autores : Carlos Mario González Vásquez, Fecha de publicación : 2019 Títulos uniformes : Radiology Case Reports Idioma : Inglés (eng) Palabras clave : Hemangioma Breast Breast neoplasms Resumen : Breast hemangioma is a rare benign tumor in female and extremely rare in males. They are part of vascular tumors. Here, we described the case of a male patient who had a breast hemangioma for 30 years that was diagnosed incidentally in a thorax and abdomen tomography. We briefly review epidemiology, histopathology, clinical, and imaging findings related to breast hemangioma Mención de responsabilidad : Sebastian Isaza Zapata, Ricardo Uribe González, Carlos Mario González Vasquez Referencia : Radiol Case Rep. 2019 Jan 16;14(4):427-429. DOI (Digital Object Identifier) : 10.1016/j.radcr.2019.01.002 PMID : 30701010 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930043318305806 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4263 Breast hemangioma in a male patient: Report of a case [documento electrónico] / Carlos Mario González Vásquez, . - 2019.
Obra : Radiology Case Reports
Idioma : Inglés (eng)
Palabras clave : Hemangioma Breast Breast neoplasms Resumen : Breast hemangioma is a rare benign tumor in female and extremely rare in males. They are part of vascular tumors. Here, we described the case of a male patient who had a breast hemangioma for 30 years that was diagnosed incidentally in a thorax and abdomen tomography. We briefly review epidemiology, histopathology, clinical, and imaging findings related to breast hemangioma Mención de responsabilidad : Sebastian Isaza Zapata, Ricardo Uribe González, Carlos Mario González Vasquez Referencia : Radiol Case Rep. 2019 Jan 16;14(4):427-429. DOI (Digital Object Identifier) : 10.1016/j.radcr.2019.01.002 PMID : 30701010 Derechos de uso : CC BY-NC-ND En línea : https://linkinghub.elsevier.com/retrieve/pii/S1930043318305806 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4263 Reserva
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Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD001242 AC-2019-031 Archivo digital Producción Científica Artículos científicos Disponible Documentos electrónicos
2019-031.pdfAdobe Acrobat PDF
