Postępy Dermatologii i Alergologii

Abstract

5/2021 vol. 38
Letter to the Editor

A case of adult-onset Still’s disease accompanied with pulmonary tuberculosis successfully treated with colchicine

  1. Department of Dermatology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China
  2. Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China
Adv Dermatol Allergol 2021; XXXVIII (5): 912-915
Online publish date: 2021/11/05
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A 54-year-old man admitted to our department presented with recurrent fever for 18 months with arthralgia and skin rash in May 2018. The patient appeared to have run a fever with no obvious cause since December 2016. His highest body temperature was 41°C, accompanied by arthralgia and myalgia, the laboratory examination showed the following: white blood cells (WBC) 12.59 × 109/l (3.5–9.5 × 109/l) with neutrophils 75.3% (40–75%); C-reactive protein (CRP) 65.8 mg/l (0–8 mg/l), erythrocyte sedimentation rate (ESR) 87 mm/h (0–15 mm/h), negative for cytomegalovirus (CMV), EBV-DNA, TORCH, ANA, ds-DNA, SSA, SSB, anti-Sm, RF, ANCA, mycoplasma, and chlamydia. Procalcitonin (PCT) 0.11 ng/ml (< 0.05 ng/ml). Pulmonary computed tomography (CT) showed nodules and chordal shadows in the right upper lung with partial calcification and mediastinal lymphadenopathy. T-spot result showed 247.4 pg/ml (< 14 pg/ml), but was negative for acid-fast staining of sputum. The patient had been in remission from pulmonary tuberculosis history for 30 years.
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