c Mycobacterium paraffinicum has been newly recognized as a species. A case of symptomatic pulmonary infection caused by M. paraffinicum is described, and as far as we know, this is the first case of the organism as a human pathogen.
CASE REPORT
In May 2012, an 85-year-old female presented to our tertiary referral hospital with acute shortness of breath. Her medical history included hypertension, for which she was not treated. She noted progressive generalized weakness, malaise, anorexia, and a chronic cough productive of white sputum for the past 6 years. On review of systems, she reported no fevers, chills, night sweats, or hemoptysis. She denied any history of smoking (but lived with a smoker), pneumonia, or other lung infections, tuberculosis exposure, homelessness, health care work, history of imprisonment, or recent travel. On physical examination, the patient had a temperature of 37.0°C, blood pressure of 158/88 mm Hg, a heart rate of 109 beats per minute (bpm), a respiratory rate of 20, and a 93% oxygen saturation as determined by pulse oximetry on ambient air. On examination, the patient had moderate kyphosis and pectus carinatum with no cervical lymphadenopathy. There was a 3/6 holosystolic murmur present at the cardiac apex and bibasilar rales on the left lung greater than on the right with no evidence of egophony. She exhibited 5/5 strength throughout all extremities. Laboratory data were as follows: white blood cell count of 16,400/l, with a differential of 1% band forms, 94% segmented neutrophils, 3% lymphocytes, and 2% monocytes, hemoglobin of 11.4 g/dl, platelet count of 507,000/l, sodium at 129 meq/liter, potassium at 3.6 meq/ liter, glucose at 131 mg/dl, and creatinine at 1.1 mg/dl. The patient was started on ceftriaxone and azithromycin for treatment of community-acquired pneumonia, which was consistent with her presentation. On the second day of hospitalization, a computed tomography (CT) scan of the chest, abdomen, and pelvis with contrast revealed near-complete occlusion of the left main bronchus with associated atelectasis of the lingula and cylindrical and cystic bronchiectasis within the left lower lobe and right middle lobe (Fig. 1). Also present were numerous nodules within the atelectatic lung, with central hypoattenuation, numerous additional nodules with central hypoattenuation present bilaterally, and moderate bilateral pleural effusions. A transthoracic echocardiogram was also obtained, revealing an impaired relaxation pattern of diastolic filling and elevated right ventricular systolic pressure. On the fourth day, the patient underwent bronchoscopy with bronchoalveolar lavage (BAL) of the left lower lobe, revealing severe mucous plugging of the left lung and thick mucoid secretions without evidence of endobronchial lesions, which grew Candida spp. Treatment of the BAL fluid with acid-fast (Kinyoun) stain revealed rare acid-fast bacilli. The infectious disease service was consulted, and PCR testing using a laboratory-developed test of the primary BAL sample was requested and was n...