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Overlapping lung parenchymal and bronchial lesion and hilar lymphadenopathy in pulmonary actinomycosis mimicking lung cancer Shino Imanishi, 1 Tsutomu Shinohara, 2 Keishi Naruse, 3 Fumitaka Ogushi 1 1 Division of Pulmonary Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan 2 Department of Clinical Investigation, National Hospital Organization Kochi Hospital, Kochi, Japan 3 Division of Pathology, National Hospital Organization Kochi Hospital, Kochi, Japan Correspondence to Dr Tsutomu Shinohara, [email protected] Accepted 13 June 2016 To cite: Imanishi S, Shinohara T, Naruse K, et al. BMJ Case Rep Published online: [ please include Day Month Year] doi:10.1136/ bcr-2016-216308 DESCRIPTION A 43-year-old man with a 9-year history of schizo- phrenia presented with productive cough, and was diagnosed with pneumonia of the left lung. As treatment with clarithromycin followed by gare- noxacin was not effective, the patient was referred to our hospital. Although physical examination was unremarkable, chest X-ray and enhanced CT showed an irregular-shaped mass in the left inferior lobe, with airway stenosis of the lobar bronchus due to wall thickness and hilar lymphadenopathy ( gure 1AC). The bronchoscopic view of swollen mucosa with nodules was compatible with lung cancer mucosal invasion ( gure 2A, B). However, mucosal biopsies revealed tiny clumps including lamentous branching of the bacteria with radial arrangement surrounded by inammatory cells ( gure 2C) and food residues. These pathological ndings were compatible with endobronchial actinomycosis. The patient was treated with paren- teral ampicillin (6 g/day) for 1 month, followed by oral amoxicillin (1.5 g/day) for 5 months. After the antibiotic treatment, chest CT showed disappear- ance of the mass shadow, airway stenosis and hilar lymphadenopathy. The patient had many risk factors for pulmonary actinomycosis, such as pre-existing dental disease, poor oropharyngeal hygiene and smoking. 1 Although pulmonary actinomycosis occasionally accompanies severe bronchial lesions, bacterial con- rmation in sputum or bronchial lavage is difcult. 2 In addition, a case of Actinomyces lymphadenitis has been reported in which lymph node biopsy revealed the characteristic sulfur granules of Actinomyces. 3 An overlapping lung parenchymal and bronchial lesion, with hilar lymphadenopathy in pulmonary actinomycosis are rare, but should be considered in the differential diagnosis of lung cancer. Figure 1 Enhanced CT showing an irregular-shaped mass in the left inferior lobe (A), with airway stenosis of the lobar bronchus due to wall thickness (B) and hilar lymphadenopathy (arrow) (C). Figure 2 Endoscopic images of swollen mucosa with nodules of the left inferior lobar bronchus (A and B) and a photomicrograph of H&E-stained mucosal biopsy, showing a tiny clump including lamentous branching of the bacteria with a radial arrangement surrounded by inammatory cells (C). Imanishi S, et al. BMJ Case Rep 2016. doi:10.1136/bcr-2016-216308 1 Images in on 17 July 2020 by guest. Protected by copyright. http://casereports.bmj.com/ BMJ Case Reports: first published as 10.1136/bcr-2016-216308 on 28 June 2016. Downloaded from
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Page 1: Images in Overlapping lung parenchymal and bronchial ...€¦ · An overlapping lung parenchymal and bronchial lesion, with hilar lymphadenopathy in pulmonary actinomycosis are rare,

Overlapping lung parenchymal and bronchial lesionand hilar lymphadenopathy in pulmonaryactinomycosis mimicking lung cancerShino Imanishi,1 Tsutomu Shinohara,2 Keishi Naruse,3 Fumitaka Ogushi1

1Division of PulmonaryMedicine, National HospitalOrganization Kochi Hospital,Kochi, Japan2Department of ClinicalInvestigation, National HospitalOrganization Kochi Hospital,Kochi, Japan3Division of Pathology,National Hospital OrganizationKochi Hospital, Kochi, Japan

Correspondence toDr Tsutomu Shinohara,[email protected]

Accepted 13 June 2016

To cite: Imanishi S,Shinohara T, Naruse K, et al.BMJ Case Rep Publishedonline: [please include DayMonth Year] doi:10.1136/bcr-2016-216308

DESCRIPTIONA 43-year-old man with a 9-year history of schizo-phrenia presented with productive cough, and wasdiagnosed with pneumonia of the left lung. Astreatment with clarithromycin followed by gare-noxacin was not effective, the patient was referredto our hospital. Although physical examinationwas unremarkable, chest X-ray and enhanced CTshowed an irregular-shaped mass in the left inferiorlobe, with airway stenosis of the lobar bronchusdue to wall thickness and hilar lymphadenopathy(figure 1A–C). The bronchoscopic view of swollenmucosa with nodules was compatible with lungcancer mucosal invasion (figure 2A, B). However,mucosal biopsies revealed tiny clumps includingfilamentous branching of the bacteria with radialarrangement surrounded by inflammatory cells(figure 2C) and food residues. These pathologicalfindings were compatible with endobronchial

actinomycosis. The patient was treated with paren-teral ampicillin (6 g/day) for 1 month, followed byoral amoxicillin (1.5 g/day) for 5 months. After theantibiotic treatment, chest CT showed disappear-ance of the mass shadow, airway stenosis and hilarlymphadenopathy.The patient had many risk factors for pulmonary

actinomycosis, such as pre-existing dental disease,poor oropharyngeal hygiene and smoking.1

Although pulmonary actinomycosis occasionallyaccompanies severe bronchial lesions, bacterial con-firmation in sputum or bronchial lavage is difficult.2

In addition, a case of Actinomyces lymphadenitis hasbeen reported in which lymph node biopsy revealedthe characteristic sulfur granules of Actinomyces.3

An overlapping lung parenchymal and bronchiallesion, with hilar lymphadenopathy in pulmonaryactinomycosis are rare, but should be considered inthe differential diagnosis of lung cancer.

Figure 1 Enhanced CT showing an irregular-shaped mass in the left inferior lobe (A), with airway stenosis of thelobar bronchus due to wall thickness (B) and hilar lymphadenopathy (arrow) (C).

Figure 2 Endoscopic images of swollen mucosa with nodules of the left inferior lobar bronchus (A and B) and aphotomicrograph of H&E-stained mucosal biopsy, showing a tiny clump including filamentous branching of thebacteria with a radial arrangement surrounded by inflammatory cells (C).

Imanishi S, et al. BMJ Case Rep 2016. doi:10.1136/bcr-2016-216308 1

Images in… on 17 July 2020 by guest. P

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eports: first published as 10.1136/bcr-2016-216308 on 28 June 2016. Dow

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Learning points

▸ Pulmonary actinomycosis should be considered in thedifferential diagnosis of lung cancer because it can presentas either or both of a parenchymal and bronchial lesion andhilar lymphadenopathy.

▸ This disease is mainly caused by aspiration of oropharyngealsecretions. Therefore, pre-existing dental disease, poororopharyngeal hygiene and smoking may be risk factors foronset.

▸ As bacterial confirmation in sputum or bronchial lavage isusually difficult, diagnosis requires additional factors such ascharacteristic pathological findings and the response toappropriate antibiotic treatment.

Contributors SI drafted the initial manuscript. TS edited and submitted themanuscript. SI and TS were involved in diagnosing and treating the patient. KNperformed the pathological studies. FO was the attending physician throughout thedisease course.

Competing interests None declared.

Patient consent Obtained.

Provenance and peer review Not commissioned; externally peer reviewed.

REFERENCES1 Valour F, Sénéchal A, Dupieux C, et al. Actinomycosis: etiology, clinical

features, diagnosis, treatment, and management. Infect Drug Resist2014;7:183–97.

2 Katsenos S, Galinos I, Styliara P, et al. Primary bronchopulmonary actinomycosismasquerading as lung cancer: apropos of two cases and literature review. Case RepInfect Dis 2015;2015:609637.

3 Arik D. Actinomyces lymphadenitis: case report. Turk Patoloji Derg 2013;29:80–2.

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2 Imanishi S, et al. BMJ Case Rep 2016. doi:10.1136/bcr-2016-216308

Images in… on 17 July 2020 by guest. P

rotected by copyright.http://casereports.bm

j.com/

BM

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eports: first published as 10.1136/bcr-2016-216308 on 28 June 2016. Dow

nloaded from