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      Natural history of Mycobacterium fortuitum pulmonary infection presenting with migratory infiltrates: a case report with microbiological analysis

      case-report

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          Abstract

          Background

          Presence of Mycobacterium fortuitum in respiratory tracts usually indicates mere colonization or transient infection, whereas true pulmonary infection occurs in patients with gastroesophageal disease. However, little is known about the diagnostic indications for true M. fortuitum pulmonary infection and the natural history of the disease.

          Case presentation

          A 59-year-old man was referred to our hospital for treatment against M. fortuitum pulmonary infection. Fifteen years before the referral, he underwent total gastrectomy, after which he experienced esophageal reflux symptoms. After the referral, the patient was closely monitored without antimicrobial therapy because of mild symptoms and no pathological evidence of M. fortuitum pulmonary infection. During the observation, chest imaging showed migratory infiltrates. Two years after the referral, his lung biopsy specimen revealed foamy macrophages and multinucleated giant cells, indicating lipoid pneumonia. However, he was continually monitored without any treatment because there was no evidence of nontuberculous mycobacterial infection. Four years after the referral, he developed refractory pneumonia despite receiving adequate antibiotic therapy. After confirmation of granulomatous lesions, multiple antimicrobial therapy for M. fortuitum resulted in a remarkable improvement with no exacerbation for over 5 years. Random amplified polymorphic DNA polymerase chain reaction analysis revealed identical M. fortuitum strains in seven isolates from six sputum and one intestinal fluid specimens obtained during the course of the disease.

          Conclusions

          We have described a patient with M. fortuitum pulmonary infection who presented with migratory infiltrates. The pathological evidence and microbiological analysis suggested that M. fortuitum pulmonary infection was associated with lipoid pneumonia and chronic exposure to gastrointestinal fluid. Therefore, physicians should carefully monitor patients with M. fortuitum detected from lower respiratory tract specimens and consider antimicrobial therapy for M. fortuitum infection when the patient does not respond to adequate antibiotic therapy against common pneumonia pathogens.

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          Most cited references18

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          A steady increase in nontuberculous mycobacteriosis mortality and estimated prevalence in Japan.

          Pulmonary disease caused by nontuberculous mycobacteria is generally reported to have a good prognosis. However, the actual mortality rate over time has not been reported in a large-scale survey. To determine the annual trend in mortality from nontuberculous mycobacteriosis, based on nearly four decades of patient data, and to estimate the prevalence of these cases in 2005. The annual mortality rate and regional distribution of nontuberculous mycobacteriosis-related deaths in Japan were obtained from Vital Statistics of Japan, which is published annually. The crude and age-adjusted mortality rates and associated regional differences were calculated from the Japanese census data. A 5-year follow-up study including 309 patients with pulmonary nontuberculous mycobacteriosis who visited and registered at our institute from 2004 to 2006 was conducted to determine the 5-year prognosis and the annual mortality rate. The crude mortality rates for both sexes have increased since 1970, and the mortality rate from pulmonary disease was greater in women after 2005. The age-adjusted rates of disease also showed a gradual increase until 2010 in women. Geographically, higher standardized mortality ratios were observed in middle and western Japan, particularly in the southern coastal regions along the Pacific Ocean. In a clinical follow-up study, the mortality rate was approximately 1-2% annually. The prevalence of pulmonary nontuberculous mycobacteriosis was estimated to be 6- to 10-fold higher than the annual incidence. There was a constant and steady increase of nontuberculous mycobacteriosis-related mortality in Japan, and this mortality rate showed significant geographical variation. The prevalence of environmental mycobacterial disease in Japan is higher than reported in most other countries.
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            Exogenous lipoid pneumonia. Clinical and radiological manifestations.

            Lipoid pneumonia results from the pulmonary accumulation of endogenous or exogenous lipids. Host tissue reactions to the inhaled substances differ according to their chemical characteristics. Symptoms can vary significantly among individuals, ranging from asymptomatic to severe, life-threatening disease. Acute, sometimes fatal, cases can occur, but the disease is usually indolent. Possible complications include superinfection by nontuberculous mycobacteria, pulmonary fibrosis, respiratory insufficiency, cor pulmonale, and hypercalcemia. The radiological findings are nonspecific, and the disease presents with variable patterns and distribution. For this reason, lipoid pneumonia may mimic many other diseases. The diagnosis of exogenous lipoid pneumonia is based on a history of exposure to oil, characteristic radiological findings, and the presence of lipid-laden macrophages on sputum or BAL analysis. High-resolution computed tomography (HRCT) is the best imaging modality for the diagnosis of lipoid pneumonia. The most characteristic CT finding in LP is the presence of negative attenuation values within areas of consolidation. There are currently no studies in the literature that define the best therapeutic option. However, there is a consensus that the key measure is identifying and discontinuing exposure to the offending agent. Treatment in patients without clinical symptoms remains controversial, but in patients with diffuse pulmonary damage, aggressive therapies have been reported. They include whole lung lavage, systemic corticosteroids, and thoracoscopy with surgical debridement. Copyright © 2010 Elsevier Ltd. All rights reserved.
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              Organising pneumonia.

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                Author and article information

                Contributors
                re_naissa@hotmail.com
                takanori.asakura@gmail.com
                tnishimura@keio.jp
                tamizu@a7.keio.jp
                ishii@keio.jp
                m-yoshida@niid.go.jp
                hfukano@nih.go.jp
                yuyucooking@gmail.com
                mfujita@fukuoka-u.ac.jp
                yhoshino@niid.go.jp
                tbetsuyaku@z5.keio.jp
                +81-3-3353-1211 , n-hasegawa@z8.keio.jp
                Journal
                BMC Infect Dis
                BMC Infect. Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                2 January 2018
                2 January 2018
                2018
                : 18
                : 1
                Affiliations
                [1 ]ISNI 0000 0004 1936 9959, GRID grid.26091.3c, Division of Pulmonary Medicine, Department of Medicine, , Keio University School of Medicine, ; 35 Shinanomachi, Shinjuku, Tokyo, 160-8582 Japan
                [2 ]ISNI 0000 0004 1936 9959, GRID grid.26091.3c, Keio University Health Center, ; 35 Shinanomachi, Shinjuku, Tokyo, 160-8582 Japan
                [3 ]ISNI 0000 0001 2220 1880, GRID grid.410795.e, Department of Mycobacteriology, Leprosy Research Center, , National Institute of Infectious Diseases, ; 4-2-1 Aobacho, Higashimurayama, Tokyo, 189-0002 Japan
                [4 ]ISNI 0000 0004 1936 9959, GRID grid.26091.3c, Division of Diagnostic Pathology, , Keio University School of Medicine, ; 35 Shinanomachi, Shinjuku, Tokyo, 160-8582 Japan
                [5 ]ISNI 0000 0001 0672 2176, GRID grid.411497.e, Department of Respiratory Medicine, Faculty of Medicine, , Fukuoka University, ; 7-45-1 Nanakuma, Jonan-ku, Fukuoka, 814-0180 Japan
                [6 ]ISNI 0000 0004 1936 9959, GRID grid.26091.3c, Center for Infectious Diseases and Infection Control, , Keio University School of Medicine, ; 35 Shinanomachi, Shinjuku, Tokyo, 160-8582 Japan
                Author information
                http://orcid.org/0000-0003-0717-7450
                Article
                2892
                10.1186/s12879-017-2892-9
                5748953
                29291713
                30a66048-31da-42a6-9a69-40bf11a38b0d
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 4 May 2017
                : 7 December 2017
                Categories
                Case Report
                Custom metadata
                © The Author(s) 2018

                Infectious disease & Microbiology
                nontuberculous mycobacteria (ntm),rapidly growing mycobacteria (rgm),aspiration,mycobacterial infection,lipoid pneumonia

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