Extract

A 27-year-old Caucasian woman presented in February 2017 with a 4-week history of symmetrical joint pain and swelling involving the ankles and knees, rash on lower limbs consistent with erythema nodosum and intermittent chest pain. No environmental triggers were identified. A chest radiograph revealed bilateral symmetrical hilar lymphadenopathy, and some atypical ill-defined air space opacities were seen in the right upper lobe (Fig. 1A). Blood tests demonstrated CRP of 199.5 mg/l (normal <5 mg/l) and serum angiotensin converting enzyme levels were 76 IU/l (normal 20–70 IU/l). A diagnosis of Lofgren’s syndrome was made. Subsequent high-resolution CT confirmed bilateral hilar lymphadenopathy and also demonstrated the galaxy sign typical of alveolar sarcoidosis (Fig. 1B). The patient made a good clinical and radiological recovery with low dose oral prednisolone, and a follow-up chest X-ray 5 months after the initial presentation showed an almost complete resolution of the atypical pulmonary opacities and improvement of the hilar lymphadenopathy

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