
Paediatric radiology
Case TypeClinical Cases
Authors
Rita Prata, Vera Carvalho, Ana Nunes
Patient16 years, female
16-year-old female presents with a 2-week history of dry cough and polyarthralgia. Her past medical history included amygdalectomy in infancy and frequent epistaxis. A lower airway infection was presumed and medicated accordingly. One week later returns with fever, dyspnea, odynophagia and presented productive cough (with 1 episode of bloody streaks).
Chest radiograph (CR) on the first admission (Figure 1). CR 1 week after starting antibiotics showed worsening opacities on both lungs, with a suggestion of cavitation in the previously noticed lower left lung opacity (Figure 2). Further characterization by non-contrast chest computer tomography (CT) showed multiple pulmonary lung nodules, both centrally and peripherally and on upper and lower lobes, some of them with a ground glass halo and two of them with central cavitation (Figures 3, 4 and 5).
Background
There were two main imaging findings in the chest CT: (1) halo sign and (2) multiple cavities. The halo sign is non-specific and its differential diagnosis includes associated haemorrhage as well as local pulmonary infiltration by neoplasm. [1]. A cavity refers to a gas-filled space in the centre of a consolidation or nodule [1].
Clinical perspective
Age, gender, history of epistaxis and polyarthralgias and the episode of bloody-streaked sputum and an elevated C reactive protein (CRP) with no leucocytosis suggests a vasculitis. Due to clinical and radiological worsening 1week after starting antibiotics a chest CT was requested, which provided more hints towards the diagnosis of vasculitis.
Imaging Perspective
Upon multiple pulmonary cavitating nodules, a radiological differential diagnosis includes the acronym “CAVIty” [2]:
Outcome: Patient was IgG class ANCA directed to proteinase 3 (ANCA PR3) positive, suggesting granulomatosis with polyangiitis [6]. Bronchofibroscopy revealed a tracheal hyperemic friable mucosa (no stenosis). Biopsy of the nasal septum mucosa, which presented whitish lesions, confirmed the diagnosis. These mucosal lesions are believed to be responsible for the past medical history of frequent epistaxis mentioned in the clinical history section above. Interestingly, regarding the other past medical history of amygdalectomy also mentioned in the same section, there is some literature suggesting these patients may have higher rates of amygdalitis [7] although we cannot prove that in our case there is any relationship between those.
Take Home Message / Teaching Points
Upon multiple pulmonary cavitating nodules, a radiological differential diagnosis includes the acronym “CAVIty”.
Persistent fever, elevated CRP, sinusitis and cavitating pulmonary infiltrates should suggest granulomatosis with polyangiitis.
Written informed patient consent for publication has been obtained.
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URL: | https://www.eurorad.org/case/17980 |
DOI: | 10.35100/eurorad/case.17980 |
ISSN: | 1563-4086 |
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