Disseminated Mycobacterium abscessus subsp. massiliense infection: case reportA 59-year-old woman developed disseminated Mycobacterium abscessus subsp. massiliense infection following treatment with prednisolone for autoimmune haemolytic anaemia and idiopathic thrombocytopenic purpura.The woman presented to a hospital with a mass on the back of her right hand. Her medical history was significant for autoimmune haemolytic anaemia (AIHA), idiopathic thrombocytopenic purpura (ITP) with splenectomy, and antiphospholipid antibody syndrome. She had been treated with prednisolone 50 mg/day [route not stated], rituximab and eltrombopag. Later, she noted a swelling on her right opisthenar and had difficulty stretching her ring finger. Her WBC count was 12 600 /µL and serum CRP level was 0.41 mg/dL. The swollen right opisthenar was suspected as benign tumour including the ganglion. Later, the mass was enlarged gradually.The woman underwent drainage and incision of the bursa at an outpatient ward. Acid-fast staining of the specimen was positive, but she was tested negative for tuberculosis and Mycobacterium avium complex. She was admitted and underwent additional curettage of the mass. Significant rice body formation was also removed. From the drainage specimens Mycobacteria was isolated. The two blood culture samples grew Gram-positive rods after 5 days. The DNA-DNA hybridization test identified the Mycobacteria as Mycobacterium abscessus complex. The bursitis were considered to due to the caused by the M. abscessus. Thus, she again hospitalised. Her right hand was swollen and reddish, and the mass measured ~40mm. Laboratory findings were as follows: elevated serum CRP, decreased haemoglobin level and thrombocytopenia. CT scan did not show any disseminated lesions. She started receiving clarithromycin, imipenem/cilastatin and amikacin. Subsequently, her right hand findings were improved. One month later, she strongly requested to be discharged. Later, she was discharged without any antibiotic therapy. Later, her blood cultures once again revealed M. abscessus complex. She underwent whole-body imaging and the following new abnormalities were noted including bilateral multiple nodular lung lesions, high signal nodules of the posterior mitral valve, lumbar disc destruction and bilateral popliteal cysts. Endocarditis was suspected. However, a clear consensus of endocarditis was not identified. Multiplex PCR revealed M. abscessus subspecies. massiliense. She again received clarithromycin, imipenem/cilastatin and amikacin for eight weeks and her blood culture was tested negative for the Mycobacterium. Her treatment was later switched to clarithromycin, sitafloxacin and faropenem. Later, faropenem was stopped and discharged with clarithromycin and sitafloxacin. In the next year, she again hospitalised with heart failure due to worsening AIHA. During admission blood culture and mycobacterial blood culture was collected. Two weeks following the admission, she died with gastrointestinal bleeding and respiratory failure. Her mycobact...