Disseminated mucormycosis with cerebellum involvement due to Rhizomucor pusillus in a patient with multiple myeloma and secondary myelodysplastic syndrome: A case report

Introduction

Mucormycosis is a rare, atypical and life-threatening zygomycosis that is mainly caused by Rhizopus species, Mucor species, Cunninghamella bertholletiae and Rhizomucor species (1–4). Mucormycosis often coexists with other underlying conditions that exhibit immunosuppression (1). Due to the characteristics of invasion of blood vessels and thrombosis, mucormysis usually exhibits rapid progression (3,4). According to the anatomical localization, infection patterns could include sinus, pulmonary, cutaneous, cerebral, gastrointestinal or kidney-related and generalized disseminated patterns (1,4–6). Rhinocerebral and pulmonary mucormycosis are the most common manifestation that occurs via air spore inhalation (6). Disseminated mucormycosis is mainly present in hematopoietic stem cell transplant recipients, and usually has a high mortality rate with >90% due to progressive invasive infection (1,7–9). The present study reports on a case of cerebral disseminated mucormycosis in a patient with multiple myeloma (MM) and secondary myelodysplastic syndrome (MDS), confirmed by mycological culture and histopathological examination.

Case report

In January 2013, a 68-year-old man visited Hangzhou First People's hospital due to backache and a fever. The initial laboratory tests showed hyperimmunoglobulin with immune globulin (Ig) A at 2.64 g/l. The 24-h κ light chain level was 6,860 mg/24 h and the serum β2-microglobulin level was 2,563 mg/l. In addition, the serum albumin level was 38.9 g/l. Bone marrow smears revealed 13.5% abnormal plasma cells. MRI determined vertebral compression fractures at T6 and T11. The pathological and flow cytometry results of bone marrow specimens with plasma cell antigens was CD117+CD38+CD138+CD56-cKappa+, and MM was diagnosed as Durie-Salmon stage II phase A and International Staging System stage I phase A.

The patient was administered chemotherapy including vincristine with 0.5 mg per day (from the first day 4), doxorubicin with 10 mg/m2 per day (10 mg/m2/d for days 1–4) and dexamethasone with 40 mg/day (days 1–4) on January 30, 2013. However, he responded poorly after two courses of chemotherapy and refused to accept bortezomib treatment, so CyRd chemotherapy comprising cyclophosphamide with 300 mg per m2 per week (300 mg/m2/w for 4 weeks), lenalidomide with 15 mg/day (from days 1–21) and dexamethasone with 40 mg per week (40 mg/w) was administered to him on 16 April, 2013. After six courses of the CyRd regimen, the patient showed a very good partial response. Thereafter, lenalidomide was used as maintenance therapy with 15 mg/day; continuous medication for 21 days with an interval of 7 days in a 28-day-course treatment.

In May 2016, the patient was admitted to Affiliated Hangzhou First People's hospital again due to disease progression with fatigue and dizziness. Bone marrow pathology and chromosome karyotyping revealed MM progression and secondary MDS. Therefore, the patient was administered bortezomib (1.3 mg/m2/week) combined with dexamethasone (40 mg; qw), but had a poor response. Since the previous chemotherapy treatment, the patient had lost weight and had been diagnosed with diabetes. However, the blood glucose levels of the patient were not well controlled due to incomplete compliance with insulin treatment.

On October 20, 2017, the patient visited the hospital after suffering from chills and fever lasting 1 week. CT showed acute pneumonia in the right middle lung (Fig. 1A and B). The cranial MRI result was normal. The results were negative with etiological separation and culture, T-SPOT test for tuberculosis infection, the galactomannan test for invasive pulmonary aspergillosis, normal cytomegalovirus DNA and endotoxin levels. The level of 1–3-β-D glucan was 550.40 ng/l. Due to the antibiotic agents having minimal effect, voriconazole (200 mg; twice per day) was empirically prescribed for antifungal treatment in considering probable invasive aspergillosis. The infection seemed to be controlled, as C-reactive protein (CRP) level and body temperature were normal. On November 24, 2017, due to the progressive MM with a level of 24-h κ light at 19,548 mg/24 h, the patient underwent chemotherapy with reduced doses of bortezomib (1.1 mg/m2/week), cyclophosphamide (300 mg; qw) and dexamethasone (20 mg; qw) due to his low weight, and the level of 24-h urine κ light chain was significantly reduced to 2543 mg/24 h. Thereafter, the patient underwent outpatient follow-up treatment.

Figure 1. Imaging findings. (A) Pulmonary CT scans showing acute pneumonia in the right middle lung (23.10.2017). (B) Pulmonary CT scans showing acute pneumonia in the right middle lung (23.10.2017). (C) Pulmonary CT scans for mucormycosis in the right lower lung (December 25, 2017). (D) Pulmonary CT scans for mucormycosis in the right lower lung (December 25, 2017). (E) MRI of the cerebellum (December 28, 2017). (F) MRI of the cerebellum (December 28, 2017). (G) MRI of the cerebellum (December 28, 2017).

During the period of outpatient follow-up treatment, the patient independently reduced the oral dose of voriconazole due to incomplete compliance. A period of 1 week later, fever presented again with a dry cough. On December 19, 2017, the patient was readmitted to Hangzhou First People's Hospital. The previous infection in the right middle lung was improved according to pulmonary CT images, but new infection sites had appeared in the right lower lung (Fig. 1C and D). MRI displayed certain abnormal signal lesions with new infection in the right cerebellum (Fig. 1E-G). At this time, combined therapy of voriconazole (200 mg, twice daily), meropenem (2.0 g, three times daily) and linezolid (0.6 g, twice daily) was started for the patient, but it was ineffective. After 10 days, the patient lost consciousness and was considered to exhibit secondary occipital foramen with high intracranial pressure. Immediately, emergency surgery was performed for decompression, showing high tension in the cerebellum, and the operation was conservative with an extremely low platelet count (18×109/l). The brain tissue showed necrosis and was obtained for histopathological and etiological examination. That night, the patient was in a persistent coma, and subsequently died due to myocardial infarction with ST-segment arch-back elevation in the multi-lead anterior intermediate wall (cardiac troponin I, 7.8 ng/ml; creatine kinase-MB, 57 ng/ml). The patient's laboratory tests and basic clinical data are presented in Table SI.

Histopathology demonstrated neutrophil infiltration and large broad-based non-septate hyphae upon Gomori methenamine silver staining, leading to a diagnosis of Mucor species (Fig. 2). Mycological cultures were positive in three days with a loose filamentous fungal colony. Both the colonial and microscopic features suggested Mucor species (Fig. 3). The antifungal susceptibility test was performed using the broth microdilution method as previously documented (10,11), and the results showed that the minimum inhibitory concentrations of posaconazole and amphotericin B were 0.25 and 1 mg/l, respectively. However, there was resistance to voriconazole and itraconazole, according to the breakpoint of Aspergillus (Table I). Internal transcribed spacer region sequencing confirmed the pathogenic basis of Rhizomucor pusillus (Genbank numbers: MN061000 and MN061001in the database of the National Center for Biotechnology Information; Fig. 3).

Figure 2. Histological analysis of a brain sample showing broad-based non-septate hyphae consistent with Mucor species following silver staining. Magnification, ×400.

Figure 3. Colonial and microscopic feature of the fungus, and ITS region sequencing. (A) Rhizomucor pusillus in blood agar. (B) ITS sequence peak maps. (C) Lactophenol cotton blue mount preparations. Magnification, ×400. ITS, internal transcribed spacer.

Table I. Minimum inhibitory concentrations of different antifungal agents.

Table I.

Minimum inhibitory concentrations of different antifungal agents.

		Breakpoint
Antifungal agentsa	MIC, mg/l	Susceptible	Intermediate	Resistant
Amphotericin B	1	≤1	2	≥4
Itraconazole	>256	≤1	2	≥4
Posaconazole	0.25	≤1	2	≥4
Voriconazole	>256	≤1	2	≥4
Anidulafungin	>8	–	–	–
Micafungin	>8	–	–	–
Caspofungin	>8	–	–	–
5-Fluorocytosine	>64	–	–	–

a The interpretive categories and MIC breakpoints are in reference to Aspergillus, according to clinical and laboratory standards institute M38 edition (CLSI M38) (11). -, no interpretive categories; MIC, minimum inhibitory concentration.

Discussion

In the present study, due to primary hematological malignancy and long-term use of chemotherapy drugs, the patient had additional high-risk factors for invasive fungal infections, including diabetes, poor immunity and immunosuppression (4,6). The patient likely contracted two different invasive fungal infections in a short time. On October 20, 2017, the patient may have been infected with a voriconazole-susceptible fungus without etiological support, because the right middle lung imaging manifestations were improved following voriconazole treatment, with the patient displaying normal CRP levels and normal body temperature. On December 19, 2017, the patient was readmitted to the hospital with a probable new fungal infection that was secondary to voriconazole treatment and was non-susceptible to voriconazole. However, when the new infection site appeared in the right lower lung and brain, the doctor incorrectly assumed the cause to be a secondary infection, in addition to the first fungal infection, and failed to identify a possible new Mucor infection. The present study concluded that if the doctor had noticed the Mucor infection, and if the patient had been appropriately treated with posaconazole, the patient may have been cured of this infection.

Although it is difficult to identify the etiological diagnosis for patients with high-risk factors due to the limited diagnostic methods (12,13) for a clinical presentation of invasive fungal infection, it is helpful to use antifungal therapy appropriately as an empirical treatment. The current report revealed that voriconazole treatment may increase the risk of Mucor infection within a short time in high-risk patients. Previous studies determined that using voriconazole, especially in patients with hematological malignancy and recipients of hematopoietic stem cell transplants, is associated with an increased incidence of mucormycosis (5,14). Mucormycosis infection can occur as a breakthrough infection during voriconazole treatment (15). The patient presented in the present case report might have had a breakthrough infection following treatment with voriconazole.

Mucormycosis is an aggressive and angioinvasive fungal infection responsible for high morbidity and mortality (6,13). Although the number of invasive mucormycosis cases has increased in recent years due to the increased prevalence of immunosuppression in the general population (7,16,17), it remains an uncommon infection (5,18). Invasive mucormycosis often occurs in high-risk populations, such as those with diabetes mellitus, hematological malignancies and other immunocompromised states (1,4,19,20). Even in immunocompetent populations, such as those with trauma, burns or undergoing surgery, invasive mucormycosis may occur, as documented in previous reports (7,12,18,19). In the present report, a patient with MM and secondary MDS demonstrated disseminated mucormycosis with cerebral involvement during voriconazole treatment. For high-risk patients who undergo voriconazole therapy, mucormycosis infection should be considered a possibility.

Due to the angioinvasive ability of mucormycosis, it can readily cause necrosis and thrombosis (21). The embolus spreads and is implanted into other sites, and may develop into disseminated mucormycosis. The central nervous system (CNS) is a common dissemination site (1,3), and the rhino-orbito-cerebral type is the predominant infection pattern (3,4). Disseminated mucormycosis is a life-threatening disease with a high mortality rate. Among 174 renal transplant recipients with mucormycosis, disseminated patterns accounted for 14.4% of cases and the mortality rate was 76.0%, compared with the overall mortality rate of 42.5% (22). In a retrospective investigation, 929 patients were diagnosed with zygomycosis, and 283 had CNS involvement with a mortality rate of 62%, with all 25 patients with generalized disseminated infection succumbing to the disease (7). In contrast to the more common rhino-orbito-cerebral mucormycosis, the infection site in the patient presented here was rare, as it occurred in the cerebellum. Disseminated cerebellar mucormycosis may have spread from the lung to the brain through the blood circulation.

To date, no common reliable clinical serological diagnostic method has been developed for mucormycosis (13,20). Histopathological examination seems to be the gold standard, as this method is able to the identify characteristic of non-septate hyphae branching at a right angle. Autopsy is another reliable invasive technique for tissue samples; however, the diagnosis rates are low, even in high-risk patients (1,6). Microbial culture is a time-consuming method with low sensitivity (17). Additionally, DNA sequencing targeting the region directly from tissue has provided a promising method for pathogenic detection (23), but sequencing is challenging in a basic laboratory setting. In most cases, high-risk patients with mucormycosis are empirically treated with antifungal therapy without histopathological and microbiological support. Thus, the diagnosis of fungal infection not only depends on the empirical work of the doctor, but is also supported by effective testing technology in the laboratory (21).

Regarding mucormycosis therapy, amphotericin B and amphotericin B lipid formulation are the most common antifungal agents for mucormycosis (5,18). Posaconazole is a novel azole antifungal for treating mucormycosis (5,24). A previous study demonstrated that antifungal treatments combined with surgical debridement are important therapies for mucormycosis (17,25).

In conclusion, the present study described disseminated mucormycosis in a patient with MM and secondary MDS. Mucormycosis can be considered a breakthrough infection in immunosuppressed patients who are receiving voriconazole therapy. In addition to early diagnosis, appropriate initiation of chemotherapy and surgical debridement are important.

Supplementary Material

Supporting Data

Acknowledgements

The authors would like to thank Dr Panpan Zhao from the Pathology Department in the Hangzhou First People's Hospital for providing the silver stain picture.

Funding

This work was supported by National Natural Science Foundation of China (grant no. 81601799), and Hangzhou Science and Technology Commission Social Development Project (grant no. 20180533B31).

Availability of data and materials

All data generated or analyzed during the present study are included in this published article and its supplementary information files.

Authors' contributions

QC and KC contributed to study design, clinical information collection, data interpretation, literature search and manuscript preparation. SXQ, XLH, PFS and KLW contributed to the collection of clinical information, the literature search and case analysis. SHW, LHX, MMW and XJW performed to the laboratory examinations, the results analysis and interpretation. All authors read and approved the final version of the manuscript.

Ethics approval and consent to participate

Informed consent was obtained from the patient.

Patient consent for publication

Informed consent for publication was obtained from the son of the patient, due to the patient passing away.

Competing interests

The authors declare that they have no competing interests.

References