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Pulmonary aspergillosis, mucormycosis, and actinomycosis co-infection presenting as a cavitary lesion in a patient with diabetes

Lin, Lan1; Xue, Dan1; Lin, Ting-Yan1; Wu, Ying-Xiao1; Jiang, Yi-Ting2; Chen, Li-Min1

Section Editor(s): Guo, Li-Shao

doi: 10.1097/CM9.0000000000000468

1Department of Respiratory Medicine, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, China

2Department of Pathology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, China.

Correspondence to: Prof. Li-Min Chen, Department of Respiratory Medicine, Fujian Medical University Union Hospital, No. 29 Xinquan Road, Fuzhou, Fujian 350001, ChinaE-Mail:

How to cite this article: Lin L, Xue D, Lin TY, Wu YX, Jiang YT, Chen LM. Pulmonary aspergillosis, mucormycosis, and actinomycosis co-infection presenting as a cavitary lesion in a patient with diabetes. Chin Med J 2019;00:00–00. doi: 10.1097/CM9.0000000000000468

Received 3 June, 2019

Online date: October 14, 2019

This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.

To the Editor: Mucormycosis and aspergillosis are opportunistic fungal infections that can lead to life-threatening complications.[1,2] Pulmonary actinomycosis is a rare infection which is commonly confused with other lung diseases.[3] Co-infection with these three pathogens in the same host is rare. Here, we report a unique case of a cavitary lesion with aspergillosis, mucormycosis, and actinomycosis co-infection.

A 52-year-old male patient with type 2 diabetes presented at Fujian Medical University Union Hospital with a 2-month history of fever, cough, expectoration, and muscle soreness. Chest computed tomography (CT) scans revealed a large irregular cavitary lesion in his right upper lobe (RUL) [Figure 1A]. Following antibacterial therapy, CT showed that his lobar pneumonia had partially disappeared but lung abscesses had formed [Figure 1B]. The sound from his right lung was slightly quieter than from the left lung; moist rales were heard from both sides.

Figure 1

Figure 1

Investigations showed elevated leukocytes (15.31 × 109/L) and serum creatinine (178 μmol/L), plus hypoxemia (arterial partial pressure of oxygen [PaO2] 66.6 mmHg). He had poor blood-glucose control (glycosylated hemoglobin 8.3%). Serum procalcitonin, fungal glucan, and Cryptococcus capsule antigen tests were negative. A serum galactomannan test (GM test) was positive (0.56). No pathogens were detected in sputum sample cultures, although Candida albicans was cultured (100 cfu/mL). Sputum smears for acid-fast bacilli and cancer cells were negative. Bronchoscopy revealed purulent sputum blocking the RUL bronchus [Figure 1E]. A bronchoalveolar lavage fluid (BALF) GM test was positive (4.51). Microbiology/pathology results confirmed aspergillosis infection.

The patient received meropenem and voriconazole for 2 weeks while aspergillosis was confirmed. CT revealed an irregular thick-walled cavity in the RUL [Figure 1C]. Oral voriconazole was continued. One month later, another bronchoscopy showed the RUL bronchus was completely obstructed by a granulomatous neoplasm [Figure 1F]; BALF GM test was positive (1.78). Pathologic results were different, with fungal mycelia observed, including Mucor [Figure 1H] and Aspergillus [Figure 1I]. Mucormycosis was confirmed; therefore, we recommended amphotericin B or posaconazole; the patient refused because he had renal dysfunction.

His intermittent fever remained; coughing, shortness of breath, and pneumonia worsened [Figure 1D]; blood creatinine increased to 260 μmol/L. Meropenem and posaconazole were given. Bronchoscopy showed the RUL bronchus completely obstructed by a yellowish granulomatous neoplasm which moved up and down as he respired [Figure 1G]. A further BALF GM test was positive (5.09). Pathology showed that fungal mycelia of Aspergillus were observed in the background of Actinomycetes [Figure 1J]. The patient refused amphotericin B again; piperacillin-tazobactam was substituted for meropenem and oral posaconazole was continued.

After 6 months, no improvement was seen, so pulmonary lobectomy was performed. Post-operative pathology showed a mycotic mass of Aspergillus. The patient went into remission.

Mucormycosis and aspergillosis are opportunistic, potentially fatal invasive fungal infections; co-infection usually occurs in the orofacial area or sinuses.[1,2] Pulmonary actinomycosis is rare and frequently confused with other pulmonary diseases; therefore, correct diagnosis is challenging, often leading to delayed or misdiagnosis.[3] Treatment of such co-infections requires prompt diagnosis, appropriate treatment, and, if necessary, surgical resection.

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Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given his consent for his images and other clinical information to be reported in the article. The patient understands that his name and initials will not be published and due efforts will be made to conceal the identity of the patient, although anonymity cannot be guaranteed.

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This work was supported by grants from the Joint Funds for the Innovation of Science and Technology, Fujian Province, China (No. 2017Y9031), Startup Fund for Scientific Research, Fujian Medical University (No. 2016QH033), and the Key Specialty Discipline Construction Program of Fujian.

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Conflicts of interest


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1. Chermetz M, Gobbo M, Rupel K, Ottaviani G, Tirelli G, Bussani R, et al. Combined orofacial aspergillosis and mucormycosis: fatal complication of a recurrent paediatric glioma-case report and review of literature. Mycopathologia 2016; 181:723–733. doi: 10.1007/s11046-016-0021-8.
2. Torres-Damas W, Yumpo-Cárdenas D, Mota-Anaya E. Coinfection of rhinocerebral mucormycosis and sinus aspergillosis [in Spanish]. Rev Peru Med Exp Salud Publica 2015; 32:813–817.
3. Boo YL, How KN, Pereira DS, Chin PW, Foonq KK, Lim SY. Pulmonary actinomycosis masquerading as lung cancer: a case report. Med J Malaysia 2017; 72:246–247.
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