Literature DB >> 30328931

Presence of gas in an unusual place: spontaneous pneumomediastinum (Hamman's syndrome).

Nicholas Oliveira Duarte1, Camila Hino Verdelho1, Rodolfo Mendes Queiroz2,3.   

Abstract

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Year:  2018        PMID: 30328931      PMCID: PMC6326704          DOI: 10.1590/S1806-37562018000000117

Source DB:  PubMed          Journal:  J Bras Pneumol        ISSN: 1806-3713            Impact factor:   2.624


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A 19-year-old male patient complained of coughing without expectoration, mild dyspnea, and retrosternal pain for three days, with no history of trauma. At physical examination, the patient presented with mild dyspnea, with no evidence of bruising or open cutaneous wounds, mildly painful crackles on bilateral supraclavicular and anterior cervical palpation, and no abnormalities on lung auscultation or laboratory test results. Chest HRCT scans revealed the presence of gas foci in the mediastinum that extended to the neck (Figure 1, arrows), which was compatible with spontaneous pneumomediastinum (Hamman’s syndrome). This is a benign, usually self-limiting disease that is more common in male patients from 17 to 25 years of age and slender body type and is characterized by the presence of air in the mediastinum that is unrelated to trauma ; the prognosis is usually excellent with conservative treatment, i.e., symptomatic treatment based on analgesia, oxygen therapy, and rest.
Figure 1

HRCT scans using axial sections, filter and lung window settings, showing the presence of laminar images with marked hypoattenuation representing gas (arrows) in deep topographies in the cervicothoracic transition and axillary regions (in A), as well as in mediastinal, paraesophageal, and paracardiac sites (in B, C and D, respectively).

  1 in total

1.  [Spontaneous pneumomediastinum: asthma].

Authors:  Marcelo Cunha Fatureto; João Paulo Vieira dos Santos; Paulo Eduardo Nunes Goulart; Samantha Andrade Maia
Journal:  Rev Port Pneumol       Date:  2008 May-Jun
  1 in total

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