Korean J Med > Volume 99(1); 2024 > Article
만성 폐쇄성 폐질환으로 저용량 스테로이드 유지 중인 환자에게 발생한 Nocardia abscessus에 의한 다발성 근육 농양 1예

Abstract

Nocardiosis is uncommon. Immunocompromising conditions predispose individuals to pulmonary and disseminated nocardiosis of the brain, skin, and subcutaneous tissues. The most common pathogens are Nocardia cyriacigeorgica, Nocardia nova, and Nocardia farcinica. The speciation of Nocardia to determine antimicrobial susceptibility is difficult using traditional biochemical methods. Here, we report the case of a 73-year-old man with chronic obstructive lung disease who developed a rapidly progressing intramuscular abscess around the left hip and thigh. Within 3 days, the lesions progressed to an epidural abscess at the L4 to S1 level. Although he was treated with broad-spectrum antibiotics and extensive incision and drainage, he died of rapidly progressive respiratory failure. Nocardia abscessus (N. abscessus) was identified in pus samples using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). This case shows that the diagnosis of an intramuscular abscess caused by N. abscessus is challenging and that using MALDI-TOF MS may facilitate the diagnosis and ensure appropriate treatment.

INTRODUCTION

Nocardia species are aerobic, Gram-positive, beaded, weakly acid-fast, branching rods. Nocardiosis results from infection by members of the genus Nocardia, which are ubiquitous environmental saprophytes that cause localized or disseminated diseases in humans via inhalation or inoculation [1]. Immunocompromised individuals with deficient cell-mediated immunity, especially that associated with lymphoma, transplantation, glucocorticoid therapy, or human immunodeficiency virus infection, are at risk for Nocardiosis [2]. Pneumonia is the most common form of Nocardia disease, and other common sites include the brain, skin and soft tissues, kidneys, joints, bones, and eyes [1-3]. Muscle involvement is rare and a typical manifestation of muscle infection is a subacute intramuscular abscess [4]. Here, we present a rare case of rapidly progressive multifocal intramuscular abscesses caused by Nocardia abscessus identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS).

CASE REPORT

A 73-year-old man presented to the emergency department with progressive back pain and pain radiating down the left leg that had worsened over the past 25 days. He also reported fever and chills. His medical history included chronic obstructive lung disease (COPD) treated with home O2 therapy, prednisolone 5 mg/day, and montelukast sodium 10 mg/day. He had received an epidural nerve block 3 days previously.
On admission, he had a temperature of 38.7℃, heart rate of 120 beats/min, and blood pressure of 87/56 mmHg. His oxygen saturation was 88% while breathing ambient air. Physical examination revealed decreased sounds in both lungs and severe tenderness of the buttocks and left thigh. The motor and sensory functions of both legs were intact. Laboratory tests revealed a white blood cell count of 45.7/µL, hemoglobin of 12.1 g/dL, platelet count of 407.0 × 103/μL, C-reactive protein level of 22.5 mg/dL (normal range, 0-0.5), procalcitonin level of 8.9 ng/mL, and lactic acid level of 3.0 mmol/L. Three sets of blood cultures on blood agar and MacConkey agar plates for 5 days were negative.
On the first day of admission, chest radiography and chest and abdominopelvic computed tomography (CT) showed extensive emphysema with chronic bronchitis, and revealed extensive intramuscular abscesses involving the left psoas, iliacus, spinalis thoracis, longissimus thoracis, gluteus maximus, and piriformis muscles (Fig. 1A, B). On the fourth day after admission, the pain in the left hip and thigh worsened despite the administration of broad-spectrum antibiotics (levofloxacin and vancomycin) and analgesics. Lumbar spine CT revealed a combined anterior epidural abscess at the L4 to S1 levels and suggested bony involvement of the left sacrum and lower lumbar spine. On the sixth day after admission, incision and pus drainage of the left iliopsoas, gluteal, and paravertebral abscesses were done to relieve pain and as definitive treatment. Yellow and brown pus was released from the psoas, iliacus, and paraspinal muscles (Fig. 1C, D). The psoas and paraspinal muscle histopathology showed many acute inflammatory cells with macrophages in a necrotic background. Gram stain and culture of pus and tissue specimens from the psoas, iliacus, and paraspinal muscles and Gram staining of surgical specimens initially showed no bacteria, but after 2 days incubation, Gram-positive filamentous rods were observed on Gram staining of cultured colonies. Four hours after the colonies were grown, the bacteria were identified as Nocardia abscessus using MALDI-TOF MS (Fig. 2). On the eighth day after admission, the acute exacerbation of COPD continued to progress, despite mechanical ventilation and the administration of high-dose steroids, and the patient died.

DISCUSSION

The organs most frequently infected by Nocardia are the respiratory tract, brain, and skin/soft tissues [1-3]. Intramuscular nocardiosis is rare; to our knowledge, only 15 cases have been reported (Table 1), including six cases each of Nocardia asteroids (N. asteroids) and Nocardia farcinica [5-8]. The psoas is the most common site of intramuscular infection due to its rich vascular nature, and a secondary psoas abscess may occur as local spread from the viscera along the iliopsoas. In an analysis of 93 psoas abscesses for which the causative microorganisms were identified over 15 years [9], there was one case of Nocardia (N. asteroides). In a literature review (Table 1), in 6/15 (40%) of cases, the muscle was the primary site of infection; in 9/15 (60%) of cases, multiple organs such as lung, brain, bone, and spleen were co-infected. Most (13/15 cases; 87%) patients were immunocompromised and three patients (cases 3, 5, and 6), including an immunocompetent patient, had jobs with a risk of Nocardia inhalation or inoculation. In our case, although 5 mg/day prednisolone is not an immunosuppressive dose, inhalation might have been a route of Nocardia infection, considering the patient’s very severe COPD with home O2 therapy and bed-ridden state.The organs most frequently infected by Nocardia are the respiratory tract, brain, and skin/soft tissues [1-3]. Intramuscular nocardiosis is rare; to our knowledge, only 15 cases have been reported (Table 1), including six cases each of Nocardia asteroids (N. asteroids) and Nocardia farcinica [5-8]. The psoas is the most common site of intramuscular infection due to its rich vascular nature, and a secondary psoas abscess may occur as local spread from the viscera along the iliopsoas. In an analysis of 93 psoas abscesses for which the causative microorganisms were identified over 15 years [9], there was one case of Nocardia (N. asteroides). In a literature review (Table 1), in 6/15 (40%) of cases, the muscle was the primary site of infection; in 9/15 (60%) of cases, multiple organs such as lung, brain, bone, and spleen were co-infected. Most (13/15 cases; 87%) patients were immunocompromised and three patients (cases 3, 5, and 6), including an immunocompetent patient, had jobs with a risk of Nocardia inhalation or inoculation. In our case, although 5 mg/day prednisolone is not an immunosuppressive dose, inhalation might have been a route of Nocardia infection, considering the patient’s very severe COPD with home O2 therapy and bed-ridden state.
As empirical antibiotics for typical intramuscular abscesses are not effective for abscesses caused by Nocardia species, identification and antibiotic susceptibility tests followed by culture should not be delayed. Since Nocardia has a low blood culture detection rate of 38% and a median incubation time of 4 days [10], incision and drainage should be performed to obtain samples as soon as possible. As intramuscular abscesses are usually subacute, there was usually sufficient time to identify the Nocardia species and prescribe specific antibiotics in most of the reported cases (Table 1). However, our patient had an acute manifestation of Nocardiosis and died before the final culture results were available. Although only 2 days were taken to identify the Nocardia abscessus (N. abscessus), incision and drainage were delayed due to the patient’s unstable general condition and were performed after the sixth day of hospitalization. Empirical antibiotics for intramuscular abscesses, such as levofloxacin and vancomycin, ultimately proved ineffective. Case 1 in the literature review (Table 1), was lost to follow-up after using penicillin without microbial identification and died 3 months later due to dissemination. We suspected Nocardia in that case because filamentous shapes were observed on Gram staining. The differential diagnosis of Gram-positive rods includes Corynebacterium, Listeria, Lactobacillus, Actinomyces (mainly as bacterial contaminants), and Nocardia species. If the Gram-positive rods are filamentous, Nocardia should be considered. Moreover, if staining for acid-fast bacilli reveals specific aerial hyphae, it helps to confirm Nocardia [1]. If cultured, Nocardia can be identified accurately using MALDI-TOF MS or 16S rRNA sequencing [1-3]. MALDI-TOF MS is used more commonly, owing to its short time and ease of use compared with 16S rRNA sequencing. The concordance between MALDI-TOF MS and 16S rRNA sequencing at the species/complex level is 97.3% [3].
The 2019 updated guidelines for Nocardia infection [10] recommended that the initial selection of an antimicrobial regimen be based on the Nocardia species. N. abscessus is generally susceptible to trimethoprim/sulfamethoxazole (TMP/SMX), amikacin, ceftriaxone, amoxicillin-clavulanic acid, tigecycline, variably susceptible to imipenem and minocycline, and resistant to ciprofloxacin, moxifloxacin, and clarithromycin/azithromycin. However, in an analysis over 10 years conducted in Spain [2], 2.8% and 4.2% of N. abscessus isolates were resistant to TMP/SMX and amoxicillin-clavulanic acid, respectively.
In summary, this case of multifocal intramuscular abscess caused by N. abscessus has educational value. Although the incidence of nocardiosis is increasing globally [10], intramuscular abscesses are still uncommon. This case highlights the importance of considering the possibility of Nocardia in patients with muscle abscesses and the value of using molecular techniques for identifying Nocardia.

Notes

CONFLICTS OF INTEREST

No potential conflicts of interest relevant to this article was reported.

FUNDING

This research was supported by the Soonchunhyang University Research Fund.

AUTHOR CONTRIBUTIONS

Conceptualization: Jung-ah Kim, Eunjung Lee, Tae Hyong Kim, Jongtak Jung, and Yae Jee Baek.

Data curation: Jung-ah Kim and Eunjung Lee.

Formal analysis: Jung-ah Kim.

Methodology: Hyunjoo Dong and Tae Youn Choi.

Writing - original draft: Jung-ah Kim and Eunjung Lee.

Writing - review & editing: Tae Youn Choi, Tae Hyong Kim, Eunjung Lee, Jongtak Jung, and Yae Jee Baek.

Acknowledgements

The authors thank the orthopedic surgeon, Sung-Woo Choi who performed incision and drainage despite the patient’s critical condition, and the respiratory physician, Youngeun Jang who provided respiratory care to the patient after surgery.

REFERENCES

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Radiological and intraoperative findings of the multifocal intramuscular abscess. (A) Abdominopelvic computed tomography reveals multiple peripheral enhancing fluid collections involving the left psoas and iliacus muscles. (B) Abdominopelvic computed tomography reveals multiple peripheral enhancing fluid collections involving the left gluteus maximus and piriformis. (C, D) A skin incision was made from 5 cm distal to the posterior superior iliac spine to 5 cm distal to the greater trochanter, and huge amounts of brownish pus gushed from the gluteus maximus.
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Figure 1.
The fingerprint of Nocardia abscessus on MALDI-TOF MS. The sample spectrum is presented at the top and the matched database spectrum below it. The best match was with Nocardia abscessus. m/z, mass to charge ratio; MALDI-TOF MS, matrix-assisted laser desorption/ionization-time of flight mass spectrometry.
/upload/thumbnails/kjm-99-1-50f2.jpg
Figure 2.
Table 1.
Clinical characteristics of muscle abscesses due to Nocardia infection: a review of literature
Case No. Age, years/sex Predisposing condition (occupation) Immuno-suppressant Parts of muscle with abscess Other organs Species (ID periodb) Treatment regimen Dose and duration Out-come
1 39/M NA NA Both psoas Brain, spleen, lung N. brasiliensis (after death) Sulfonamide NA Died
2 44/M KT, valvular heart disease Cyclosporine, prednisolone Right psoas,a gluteus maximus - NA (17 days) TMP/SMX NA Cured
3 61/M CLL (gardener) Cyclo-phosphamide, vincristine Right psoas Lung N. asteroides Minocycline 100 mg ql2h, 4 months Cured
4 61/M KT Cyclosporine, azathioprine, prednisolone Right biceps brachii Lung N. asteroides TMP/SMX NA, 12 months Cured
5 5&M HT (gardener) Cyclosporine, azathioprine Left adductor - N. asteroides TMP/SMX 960 mg ql2h, 1 year Cured
6 42/M - (cattle inspector) - Left psoas - N. farcinica (17 days) TMP/SMX 10 mg/kg q24h and 50 mg/kg q24h, 11 months Cured
7 40/M Wound dehiscence after 3rdKT Prednisolone, mycophenolate mofetil, tacrolimus Right deltoid Lung N. asteroides TMP/SMX 800 mg ql2h and 160 mg ql2h, 2 weeks Cured
400 mgql2h and 80 mg ql2h, 1 year
8 32/F SLE, lupus nephritis Cyclo-phosphamide, prednisolone Left deltoid - N. farcinica (12 days) TMP/SMX NA Cured
9 65/F Hodgkin’s lymphoma Methotrexate, vinblastine, bleomycin Right vastus lateralis - N. farcinica TMP/SMX 160 mg ql2h and 800 mg ql2h, 3 months Cured
10 76/M Suspicion of Rheumatic disorder Corticosteroid Left gracilis - N. farcinica TMP/SMX 1,920 mgql2h, 3 months Cured
11 46M Obesity, alcoholism - Ilio-psoas Maxilla,a spinal disk N. asteroides (7 days) Imipemen, amikacin, rifampin NA, 4 months Cured
12 32/M AIDS, hepatitis C, alcoholism - Left paravertebral, psoas, maximus gluteusa Lung N. asteroides TMP/SMX, ciprofloxacin NA Cured
13 61/F SLE, lupus nephritis Prednisolone Left psoas Lung N. farcinica TMP/SMX ceftriaxone, ciprofloxacin 160-800 mg q8h, 9 days (azotemia) Cured
2 g q24h, 4 weeks
200 mg ql2h, 12 weeks
14 59/F Autoimmune hemolytic anemia Prednisolone Left biceps femorisa Lung, brain N. farcinica (9 days) TMP/SMX, imipemen, amikacin 4,000-9,000 mg q24h, 9 months Cured
2,000 mg q24h, 5 months
800 mg q24h, 5 months
15 79/M Myasthenia gravis Steroid Both biceps femoris Lunga N. pseudo-brasiliensis Linezolid, moxifloxacin NA, 3 weeks (thrombocyto-penia) Cured
NA, 6 months
This case 73/M COPD, recurrent pneumo-thorax Prednisolone, dexamethasone Left psoas,a iliacus, spinalis thoracis, longissimus thoracis, gluteus maximus, piriformis - N. abscessus (2 days) Levofloxacin, vancomycin 750 mg q24h, 7 days Died
900-1,000 mg ql2h, 7 days

ID, identification; M, male; NA, not available; N. brasiliensis, Nocardia brasiliemsis; KT, kidney transplantation; TMP/SMX, trimethoprim/sulfamethoxazole; CLL, chronic lymphocytic leukemia; N. asteroides, Nocardia asteroids; HT, heart transplantation; N. farcinica, Nocardia farcinica; F, female; SLE, systemic lupus erythematosus; AIDS, acquired immune deficiency syndrome; COPD, chronic obstructive pulmonary disease; N. pseudo-brasiliensis, Nocardia pseudo-brasilieusis; N. abscessus, Nocardia abscessus.

a Primary organ of infection suspected by the authors of the literature.

b Period until identifying Nocardia after hospitalization.

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