Pulmonary artery hypertension associated with systemic scleroderma: Correlation among lung pulmonary blood volume, lung perfusion single photon emission computed tomography, and chest computed tomography images

摘要

A 68-year-old woman had been experiencing Raynaud symptom, palpitation of the heart, and short breath in walking stairs or slopes for 7 years. Recently, these symptoms had rapidly become worse. She admitted to our hospital. At that time, she was diagnosed with systemic scleroderma (limited scleroderma). Pulmonary hypertension was pointed out by echocardiography (estimated pulmonary artery pressure 35-43 mm|Hg), and she was suspected as having pulmonary artery hypertension associated with systemic scleroderma. At the admission, laboratory data showed as follows: plasma D-dimer 0.2 mug/mL, IgM 419.3 mg/dL, antinuclear antibody x640, anticentromere antibody 140.6 index (+), and anti-Scl-70 antibody 2.7(-). Respiratory function test showed vital capacity 1.26 L, percentage of vital capacity 59.7%, percentage of forced expiratory volume in one second 80.8%, and percentage of carbon monoxide diffusing capacity 45.1%.