Spontaneous Pneumomediastinum: Analysis of 62 Consecutive Adult Patients
نویسندگان
چکیده
منابع مشابه
Spontaneous pneumomediastinum in adult dermatomyositis.
Spontaneous pneumomediastinum has not been reported in adult polymyositis or dermatomyositis, either in conjunction with spontaneous pneumothorax or in isolation. Spontaneous pneumothorax has been rarely reported as a complication of rheumatoid arthritis, systemic lupus erythematosus, scleroderma, and childhood dermatomyositis. It is associated with active, progressive pulmonary involvement and...
متن کاملClinical Analysis of Spontaneous Pneumomediastinum
BACKGROUND Spontaneous pneumomediastinum is a rare and benign condition that generally occurs in young generations without any precipitating factor or underlying disease. The purpose of this study is to review our experience in dealing with this entity and detail a reasonable course of assessment and management. METHODS From December 1999 to May 2012, 32 spontaneous pneumomediastinum patients...
متن کاملProlonged spontaneous pneumomediastinum in adult dermatomyositis.
SIR, We read with great interest Dr Bradley's first reported case of pneumomediastinum in an adult with dermatomyositis.' We describe here a similar event, where spontaneous pneumomediastinum occurred in a patient with dermatomyositis and persisted for five months. In January 1986 a 20 year old man was admitted to hospital for assessment of recent generalised muscle, weakness. Examination showe...
متن کاملRecurrent spontaneous pneumomediastinum in an adult.
Spontaneous pneumomediastinum (SP) is defined as the presence of free air in mediastinal space without any apparent cause. This rare entity is most likely to occur in young males often related to an episode of vomiting, asthma or sustained physical activity. SP usually resolves spontaneously in few days of treatment based on rest and analgesia. Complications are extremely rare. Its recurrence h...
متن کاملSpontaneous pneumomediastinum
A 17-year-old white female presented to the emergency department with chest pain 12 h after ingesting four pills of phentermine (Adipex®). She complained of retrosternal chest pain radiating into her neck with inspiration. Medical history was unremarkable, and she denied any other medications or illicit drug use. Vital signs were normal with 100% pulse oximetry. Physical examination revealed no...
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ژورنال
عنوان ژورنال: Mayo Clinic Proceedings
سال: 2009
ISSN: 0025-6196
DOI: 10.1016/s0025-6196(11)60560-0