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1.
Clin Med (Lond) ; 23(5): 518-520, 2023 09.
Artículo en Inglés | MEDLINE | ID: mdl-37775170

RESUMEN

Refractory hypoglycaemia in a patient with a solitary fibrous tumour (SFT) is very rare and was first reported in 1930 independently by Doege and Potter, leading to it being named 'Doege-Potter syndrome'. Here, we report the unusual case of a 77-year-old woman with a giant solitary fibrous pleural tumour who presented with complicating pulmonary hypertension and associated heart failure with hypoglycaemia, and subsequently underwent curative resection of the pleural mass with clinical improvement.


Asunto(s)
Hipertensión Pulmonar , Hipoglucemia , Tumor Fibroso Solitario Pleural , Femenino , Humanos , Anciano , Hipertensión Pulmonar/etiología , Tumor Fibroso Solitario Pleural/diagnóstico , Tumor Fibroso Solitario Pleural/diagnóstico por imagen , Síndrome , Hipoglucemia/etiología
2.
Clin Med (Lond) ; 20(6): e262-e263, 2020 11.
Artículo en Inglés | MEDLINE | ID: mdl-33199333

RESUMEN

Why we only infrequently detect or report two or more respiratory viruses co-infecting an adult host is poorly understood. We report a rare case where influenza B and SARS-CoV-2 caused viral pneumonia in a 74-year-old man diagnosed during the UK winter epidemic/pandemic for these organisms and discuss concepts of co-infection.


Asunto(s)
Coinfección , Infecciones por Coronavirus , Virus de la Influenza B , Gripe Humana , Pandemias , Neumonía Viral , Anciano , Betacoronavirus , COVID-19 , Infecciones Comunitarias Adquiridas , Presión de las Vías Aéreas Positiva Contínua , Humanos , Pulmón/diagnóstico por imagen , Pulmón/patología , Masculino , SARS-CoV-2
3.
Clin Med (Lond) ; 2020 May 05.
Artículo en Inglés | MEDLINE | ID: mdl-32371417

RESUMEN

A 40-year-old man developed acute brainstem dysfunction 3 days after hospital admission with symptoms of the novel SARS-CoV-2 infection (COVID-19). Magnetic resonance imaging showed changes in keeping with inflammation of the brainstem and the upper cervical cord, leading to a diagnosis of rhombencephalitis. No other cause explained the patient's abnormal neurological findings. He was managed conservatively with rapid spontaneous improvement in some of his neurological signs and was discharged home with continued neurology follow up.

4.
BMJ Case Rep ; 13(5)2020 May 11.
Artículo en Inglés | MEDLINE | ID: mdl-32398248

RESUMEN

Drug rash occurring with eosinophilia and systemic symptoms syndrome is a potentially fatal adverse drug reaction that requires immediate action in order to minimise patient harm. Initially implicated with the use of anticonvulsants, it has also been shown to be caused by many other medications but less frequently with vancomycin. Patients typically present with fever, lymphadenopathy, eosinophilia and systemic organ dysfunction. Diagnosis is aided using probability calculators such as RegiSCAR (Registry of Severe Cutaneous Adverse Reaction), as well as clinical response on removing the responsible medication. Here, we present a case without any systemic organ dysfunction that improved with withdrawal of the offending drug vancomycin.


Asunto(s)
Lesión Renal Aguda/inducido químicamente , Síndrome de Hipersensibilidad a Medicamentos/etiología , Eosinofilia/inducido químicamente , Vancomicina/efectos adversos , Anciano , Antibacterianos/administración & dosificación , Antibacterianos/efectos adversos , Diagnóstico Diferencial , Femenino , Humanos , Absceso Pulmonar/tratamiento farmacológico , Fumadores , Vancomicina/administración & dosificación
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