RESUMEN
A 45-year-old man with a raised body mass index presented with an acute history of right lower chest pain and increasing breathlessness. C reactive protein, D dimer and cardiac echocardiography were negative, with mild bibasal atelectasis the only positive reported finding from erect chest X-ray and CT pulmonary angiogram. He was discharged with antibiotics for a chest infection. He remained severely breathless and was referred to the sleep-related breathing disorders clinic. He described shoulder pain, daytime tiredness and sleeping upright due to a ââ'¬ËÅsuffocatingââ'¬â"¢ sensation. The video demonstrates the clinical findings. The CT topogram confirmed bilateral diaphragmatic paralysis. Spirometry demonstrated an 80% reduction in forced vital capacity in the supine position, when compared with erect. Consultation with a neurologist yielded the diagnosis of neuralgic amyotrophy, leading to bilateral diaphragmatic paralysis. The respiratory symptoms have been controlled with night-time non-invasive ventilation, allowing him to sleep supine.
Asunto(s)
Neuritis del Plexo Braquial/complicaciones , Diafragma/patología , Disnea/etiología , Parálisis Respiratoria/etiología , Dolor de Hombro/etiología , Neuritis del Plexo Braquial/diagnóstico , Diafragma/inervación , Disnea/diagnóstico , Humanos , Masculino , Persona de Mediana Edad , Ventilación no Invasiva , Nervio Frénico , Parálisis Respiratoria/diagnóstico , Dolor de Hombro/diagnóstico , EspirometríaRESUMEN
Hypereosinophilic syndrome is a disease characterised by a persistently elevated eosinophil count. The syndrome can be reactive to infections, autoimmune disease, cancers, etc. Multiple organ involvement can occur including cardiomyopathies, pulmonary involvement and neuropathies. We describe a case of a patient who presented with signs and symptoms of asthma with recurrent asthma exacerbations, but in fact proved to be hypereosinophilic syndrome secondary to strongyloides infection.
Asunto(s)
Asma/etiología , Síndrome Hipereosinofílico/etiología , Estrongiloidiasis/complicaciones , Adulto , Diagnóstico Diferencial , Progresión de la Enfermedad , Femenino , Humanos , Estrongiloidiasis/tratamiento farmacológico , Tomografía Computarizada por Rayos XRESUMEN
Surgical emphysema associated with an acute asthma exacerbation is very rare. This report presents the case of a 19- year-old male patient with a background of asthma who presented with palpable cervical surgical emphysema and CT evidence of mediastinal emphysema. There are only a limited number of case reports associated with surgical emphysema in the absence of pneumothorax in patients with an asthma exacerbation. Evidence with regard to the management of such cases is limited and is largely consensus based. Below we discuss the case in a greater detail.
Asunto(s)
Asma/complicaciones , Enfisema Mediastínico/etiología , Enfisema Subcutáneo/etiología , Asma/diagnóstico por imagen , Humanos , Masculino , Dolor de Cuello/etiología , Tomografía Computarizada por Rayos X , Adulto JovenRESUMEN
Simultaneous bilateral spontaneous pneumothoraces (SBSP) are uncommon. This report presents the case of a previously well 19-year-old man with a diagnosis of SBSP and symptoms suggestive of occupational asthma. Despite bilateral bullectomy and pleurodesis using a video-assisted thoracoscopic surgical technique, the pneumothorax reoccurred unilaterally and open surgery was performed. This case illustrates a rare condition of bilateral pneumothoraces presenting as a first presentation of occupational asthma and the issues surrounding its management.