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Inicio Enfermedades Infecciosas y Microbiología Clínica (English Edition) Microbiology of breast abscesses
Información de la revista
Vol. 40. Núm. 9.
Páginas 479-482 (noviembre 2022)
Visitas
1951
Vol. 40. Núm. 9.
Páginas 479-482 (noviembre 2022)
Original article
Acceso a texto completo
Microbiology of breast abscesses
Microbiología de los abscesos mamarios
Visitas
1951
Joaquín Bartolomé-Álvarez
Autor para correspondencia
jbartolome@sescam.jccm.es

Corresponding author.
, Verónica Solves-Ferriz
Servicio de Microbiología, Complejo Hospitalario Universitario de Albacete, Albacete, Spain
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Abstract
Introduction

Treatment of breast abscesses is based on drainage and antibiotic therapy directed at the bacteria causing the infection. The aim of this study was to know the etiological agents of breast abscesses.

Methods

Patients who had a culture-positive breast abscess between September 2015 and January 2020 were included in the study. Culture results were consulted in the laboratory database. It was collected from medical records if the patients presented the following risk factors: breastfeeding, diabetes or smoking. Abscesses secondary to surgical wound infection were excluded.

Results

Sixty patients were included, 58 women and 2 men. Staphylococcus aureus was the most frequent agent in lactating women. Anaerobic bacteria were isolated in 28 (61%) of 46 abscesses in non-lactating patients. In non-lactating patients, the frequency of anaerobes in abscesses was lower in diabetics than in the rest (0/5 vs 26/38; P = .013). In non-lactating and non-diabetic patients, the proportion of abscesses with anaerobes was higher in smokers than in non-smokers (21/24 vs 5/14; P = .003). Aerobic gram-positive cocci were the most frequent agents in diabetics.

Conclusion

Anaerobes were the most frequent agents, followed by S. aureus. The etiology of breast abscesses varied with the risk factors studied.

Keywords:
Breast abscess
Anaerobes
Microbiology
Staphylococcus epidermidis
Resumen
Introducción

El tratamiento de los abscesos mamarios se basa en el drenaje y la antibioticoterapia dirigida a las bacterias causantes de la infección. El objetivo de este estudio fue conocer los agentes etiológicos de los abscesos mamarios.

Métodos

Se incluyó en el estudio a los pacientes que, entre septiembre de 2015 y enero de 2020, tuvieron un absceso mamario con cultivo positivo. Se consultaron los resultados de los cultivos en la base de datos del laboratorio. Se recogió de las historias clínicas si los pacientes presentaban los siguientes factores de riesgo: lactancia, diabetes o hábito fumador. Se excluyeron los abscesos secundarios a una infección de herida quirúrgica.

Resultados

Se incluyeron 60 pacientes, 58 mujeres y 2 varones. Staphylococcus aureus fue el agente más frecuente en mujeres lactantes. Se aislaron bacterias anaerobias en 28 (61%) de los 46 abscesos en pacientes no lactantes. En los no lactantes, la frecuencia de anaerobios en los abscesos fue menor en diabéticos que en el resto (0/5 frente a 26/38; P = ,013). En los no lactantes y no diabéticos, la proporción de abscesos con anaerobios fue mayor en fumadores que en no fumadores (21/24 frente a 5/14; P = ,003). Los cocos grampositivos aerobios fueron los agentes más frecuentes en los diabéticos.

Conclusión

Los anaerobios fueron los agentes más frecuentes, seguidos por S. aureus. La etiología de los abscesos mamarios varió con los factores de riesgo estudiados.

Palabras clave:
Absceso mamario
Anaerobios
Microbiología
Staphylococcus epidermidis
Texto completo
Introduction

Breast abscesses lead to considerable morbidity. They have a tendency to recur and can cause permanent sequelae, such as deformities of the breast or loss of ability to produce milk1. Breast-feeding women, smokers and diabetic patients are at increased risk for breast abscess1–3. Treatment is based on drainage and administration of antibiotics1. The selection of empirical antibiotic therapy for breast abscesses should target the bacteria that most commonly cause these infections.

Studies on the microbiology of breast abscesses published to date indicate that there are a variety of bacterial species that can cause these infections, and demonstrate mixed results in terms of the relative contribution of different species or groups of bacteria2,4–20. These disparities in the results of published studies may be due, at least in part, to differences in the screening criteria of the subjects and in the methodology adopted to carry out the cultures and interpret their results. The factors that make it difficult to compare different studies include: a) the fact that some studies include post-surgical infections along with primary breast abscesses, or puerperal and nonpuerperal abscesses, and do not provide disaggregated results2,10,11,16,17,19,20; b) the fact that most publications, especially the most recent ones, do not describe the methodology used to carry out the cultures, and in particular whether or not the culture has been carried out for anaerobic bacteria2,8–10,12,14,15,17–20; c) the fact that almost all of the published papers lack a description of the criteria used to interpret the cultures, which is especially important when it comes to attributing relevance to skin commensal bacterial species and common contaminants of cultures. This article studies the aetiology of primary breast abscesses using strict and explicit criteria to screen subjects, perform microbiological studies and interpret culture results. The objective of this study was to discover the aetiological agents of breast abscesses in our setting.

Materials and methods

Patients who had a breast abscess with a positive culture between September 2015 and January 2020 were retrospectively studied. The source of information for patient screening was the Microbiology Laboratory database. Direct microscopic examination of all breast abscess samples received in the laboratory was performed, and those with one or more epithelial cells per low-power field (100×) were excluded from the study. The following culture media were spiked with samples: blood agar, chocolate agar, blood agar with colistin and nalidixic acid (incubated at 35 °C in air with 5% CO2 for at least three days), MacConkey agar (incubated one day in air at 35 °C), Schaedler agar and Schaedler agar with vancomycin and kanamycin (incubated at 35 °C in anaerobiosis for at least five days). A thioglycolate broth was also spiked and incubated at 35 °C for at least five days. Becton Dickinson (BD, Sparks, MD, USA) supplied the culture media until January 2019. Thereafter, BD supplied the Schaedler agar, the Schaedler agar with vancomycin and kanamycin and the thioglycolate broth, while bioMérieux (Marcy l'Étoile, France) supplied the rest of the culture media. Isolated microorganisms were identified by mass spectrometry (MALDI-TOF MS, bioMérieux), and species-level identifications with a 99.9% confidence level were considered valid. Limited growth of bacteria typical of the skin flora (coagulase-negative Staphylococcus, Corynebacterium and Cutibacterium) was deemed insignificant and ignored, except in the following cases: 1) the isolation in pure culture of Staphylococcus lugdunensis was always deemed significant, because its capacity to cause breast abscesses is understood21; 2) the isolation of other coagulase-negative Staphylococcus was deemed significant if direct microscopic examination of the sample showed staphylococcal-compatible intraleukocytic Gram-positive cocci and no other Gram-positive cocci were isolated from the culture (own criterion); 3) the isolation of Corynebacterium kroppenstedtii was always deemed significant22; 4) following previously published criteria23, the isolation of other Gram-positive diphtheria-producing bacilli was deemed significant if the following four conditions were met: pure or predominant diphtheria-producing culture; b) direct microscopic examination of the sample with Gram-positive bacilli or >1 neutrophil per 100× field; c) presence in the patient of an erythematous or purulent lesion with clinical suspicion of infection; and d) the clinician agreed that the isolate was the cause of the infection, or moderate or abundant growth of the isolate was observed in the culture, and the clinical picture was highly suggestive of a role in infection23. The presence of anaerobic bacteria in the culture was confirmed by the aerotolerance test (simultaneous subculture of chocolate agar, incubating it for 48 h at 37 °C in aerobiosis with 5% CO2, and Schaedler agar, incubating it for 48 h at 37 °C in anaerobiosis). If more than two morphotypes of anaerobic bacteria were observed in the culture without predominance of any of them, it was reported as mixed anaerobic flora. If there were one or two predominant anaerobic morphotypes, they were identified. Strains of Actinomyces were counted among anaerobes, even if they showed growth in aerobiosis. A polymicrobial infection was identified if more than one significant microorganism was isolated. The results of the cultures were obtained from the laboratory database. Medical histories were reviewed and information was collected regarding the status of diabetic, smoker or breast-feeding mother, as well as the method of obtaining the culture sample. Abscesses secondary to a surgical wound infection were excluded. If a patient had more than one episode of breast abscess in the study period, only the first was considered, regardless of the microorganism that was isolated in subsequent episodes. The reason for this is that if all episodes were included, the microorganisms that most often caused recurrences would be overrepresented. Fisher's exact test was used to compare proportions.

Results

Sixty patients met the inclusion criteria for the study: 58 women and two men, with a mean age of 40 years (standard deviation [SD] = 12 years). Of these, 55 had a medical history containing sufficient information on all risk factors considered (breastfeeding, diabetes, smoking). Abscess samples for culture were obtained in 44 cases by percutaneous needle aspiration, in 15 cases by incision and surgical drainage, and in one patient the spontaneous drainage material was collected with a swab with anaerobic transport medium. Table 1 shows the culture results of the 60 abscess samples. All microorganisms were isolated from the primary plates. Anaerobic bacteria were the most common agents, followed by Staphylococcus aureus. Table 2 shows the species of anaerobic bacteria that were isolated as predominant morphotypes or as pure culture. Finegoldia magna was the most common anaerobic species. All strains of S. aureus were methicillin-susceptible. All strains of Corynebacterium and coagulase-negative Staphylococcus (including S. lugdunensis) were isolated from samples obtained by needle aspiration or surgical drainage.

Table 1.

Culture results for the 60 abscess samples.

  Number of patientsa
  Total (n = 60)  Breast-feeding (n = 12)  Not breast-feeding
Culture result      Total (n = 46)  Diabetic (n = 5)  Not diabetic (n = 38) 
Pure culture
S. aureus  16  10 
Coag.-neg. Staph. b  − 
Aerobic GNB [Gram-negative bacilli]c 
Corynebacteriumd  −  − 
Streptococcus agalactiae  −  – 
Anaerobese  −  − 
Polymicrobial infection
Only anaerobes  25  −  24  −  23 
Aerobesf/anaerobes  − 
Only aerobesg  −  − 
a

In 2 of the 60 patients it was not possible to rule out the possibility that they were breast-feeding mothers, and in 3 of the 46 patients who were not breast-feeding it was not possible to rule out the possibility that they were diabetic. Therefore, in the table the sum of patients who were breast-feeding and patients who were not breast-feeding does not equal the total (60), and the sum of diabetics and non-diabetics does not equal the total of patients who were not breast-feeding (46).

b

Coagulase-negative Staphylococcus: S. epidermidis: 2, S. lugdunensis: 1.

c

Escherichia coli: 2, Proteus mirabilis: 2, Pseudomonas aeruginosa: 1.

d

C. kroppenstedtii: 3, C. tuberculostearicum: 1.

e

Unidentified diphtheria-producing Gram-positive bacillus: 1.

f

Aerobes: S. aureus: 1, S. lugdunensis: 1, S. epidermidis: 1, Streptococcus anginosus: 1.

g

Streptococcus intermedius and S. anginosus: 1.

Table 2.

Distribution by species of anaerobic bacteria isolated in pure or predominant culture.

  Samples, n 
Gram-positive   
Finegoldia magna 
Cutibacterium avidum 
Peptostreptococcus anaerobius 
Peptoniphilus asaccharolyticus 
Actinomyces neuii 
Actinomyces europaeus 
Unidentified diphtheria-producing GPB [Gram-positive bacilli]a 
Gram-negative   
Campylobacter ureolyticus 
Prevotella timonensis 
Prevotella bivia 
Fusobacterium necrophorum 
Unidentified Gram-negative bacillia 
Unidentified Gram-negative coccia 
a

The MALDI-TOF MS system software did not provide identification.

Abscesses in breast-feeding women

Twelve patients were breast-feeding mothers, with a mean age of 34 years (SD = 5.3 years), nine of whom were primiparous. S. aureus was the most common agent in breast-feeding patients (Table 1).

Abscesses not associated with breastfeeding

The mean age of patients who were not breast-feeding was 42 years (SD = 12 years). Anaerobic bacteria were isolated in 28 (61%) of the 46 abscesses, and 25 (54%) were found to be purely anaerobic (Table 1). The proportion of abscesses in which anaerobic bacteria were isolated was lower in diabetics than in the rest of the patients (0 out of 5 versus 26 out of 38, respectively; P = .013). In non-diabetics, the proportion of anaerobic abscesses was higher in smokers than in non-smokers (21 out of 24 versus 5 out of 14, respectively; P = .003). In four of the five diabetic patients, the infection was caused by an aerobic Gram-positive coccus (Table 1).

C. kroppenstedtii was isolated in three women with subareolar abscesses. All three women were treated with drainage (surgical in two cases and needle aspiration in the third) and antibiotic therapy. One of the patients subsequently had several recurrences in both breasts with repeated positive cultures (two from each breast) for C. kroppenstedtii, despite being treated with several cycles of antibiotics to which the bacterium was susceptible in vitro. The second patient received three cycles of treatment with antibiotics active in vitro over five months due to the persistence of the abscess, which finally resolved. The third patient did not return for a consultation and there are no follow-up data. She had had a breast abscess nine months earlier at the same location, which was drained without a microbiological study.

In three patients, aged 55, 63 and 73 years, there was significant isolation of Staphylococcus epidermidis; pure culture in two cases (Table 1). Microscopic examination of the samples revealed moderate (one case) or abundant (two cases) leukocytes and intraleukocytic Gram-positive cocci. The growth in culture of S. epidermidis was moderate in two cases and abundant in one. In one case, moderate growth of an unidentified anaerobic Gram-negative bacillus was also obtained. All three patients were treated with needle aspiration drainage and antibiotic therapy to which the isolated strains were susceptible in vitro. The abscesses resolved in two cases (including polymicrobial infection). The third patient underwent further drainage a month later (without microbiological study) because the lesion persisted, and subsequently did not attend a consultation, so there are no more follow-up data.

Discussion

In this retrospective study, methicillin-susceptible S. aureus was the most common agent in breast abscesses in breast-feeding women. A greater variety of aetiological agents was found in breast abscesses in women who were not breast-feeding, with a predominance of anaerobic bacteria.

There are only two studies that have been carried out in Spain on the microbiology of nonpuerperal breast abscesses, both by the same group of researchers and both published in 199510,11. These studies, which partially overlap, include patients with surgical infections and primary breast abscesses without disaggregating the results, so it is difficult to compare their results with those of our study. The lower proportion of anaerobes found in these studies may be due to the studies' inclusion of patients with abscesses secondary to surgery10,11.

Our study has demonstrated the importance of anaerobic bacteria in abscesses not associated with breast-feeding, particularly in smokers, who represented a significant proportion of patients in our series (24 of the 38 patients who were non-diabetic and not breast-feeding were smokers). Previous studies have also found an association between smoking and the presence of anaerobes in breast abscesses9,14. In our study, we found anaerobes in 61% of abscesses in patients who were not breast-feeding. Examination of the literature reveals that the proportion of primary breast abscesses with anaerobes ranges from 44% to 93% in publications that state that anaerobic culture has been performed4–7. In contrast, the percentage of abscesses with anaerobes varies between 25% and 42% in studies that do not claim to have performed anaerobic culture of all samples9,12,15,18,20. This difference underscores the importance of adequate microbiological documentation in studies on the aetiology of these infections. With regards to the most relevant anaerobic species, the significance of Finegoldia magna and the absence of Bacteroidesis striking, which is consistent with previously published results24.

Although our study does not include many diabetic patients, the results suggest that breast abscesses in these patients have a differentiated microbiology, with a lower presence of anaerobes. Confirmation of these findings is needed in studies with more patients.

Two cases of breast abscess due to S. epidermidis and one case of polymicrobial abscess involving S. epidermidis were documented in this study. There is no description in the literature of a primary breast abscess due to coagulase-negative Staphylococcus, other than S. lugdunensis, for which case the criteria used to give it clinical significance are explained. Coagulase-negative Staphylococcus appear in many publications in the list of isolated microorganisms and are among the most common in some studies7,8,13,19,20, but without an explanation of the criteria that have been followed to give them clinical significance. In a proven case of primary breast abscess due to coagulase-negative Staphylococcus, the species was not determined25. Our results indicate that S. epidermidis can cause primary breast abscesses, although this is not common. It is also worth noting the older age of patients with significant isolation of S. epidermidis.

In conclusion, the aetiology of breast abscesses varied with the patient's risk factors. S. aureus predominated in breast-feeding mothers, anaerobes in smokers, and aerobic Gram-positive cocci in diabetics. These risk factors should be considered in future studies on the aetiology and antibiotic therapy of breast abscesses.

Conflicts of interest

None.

References
[1]
E. Boakes, A. Woods, N. Johnson, N. Kadoglou.
Breast infection: a review of diagnosis and management practices.
Eur J Breast Health., 14 (2018), pp. 136-143
[2]
V. Gollapalli, J. Liao, A. Dudakovic, S.L. Sugg, C.E.H. Scott-Conner, R.J. Weigel.
Risk factors for development and recurrence of primary breast abscesses.
J Am Coll Surg., 211 (2010), pp. 41-48
[3]
M. Rizzo, L. Peng, A. Frisch, M. Jurado, U. Umpierrez.
Breast abscesses in nonlactating women with diabetes: clinical features and outcome.
Am J Med Sci., 338 (2009), pp. 123-126
[4]
I. Brook.
Microbiology of non-puerperal breast abscesses.
J Infect Dis., 157 (1988), pp. 377-379
[5]
A.W. Sturm.
Mobiluncus species and other anaerobic bacteria in non-puerperal breast abscesses.
Eur J Clin Microbiol Infect Dis., 8 (1989), pp. 789-792
[6]
A.P. Walker, C.E. Edmiston, C.J. Krepel, R.E. Condon.
A prospective study of the microflora of nonpuerperal breast abscess.
[7]
C.E. Edmiston, A.P. Walker, C.J. Krepel, C. Gohr.
The nonpuerperal breast infection: aerobic and anaerobic microbial recovery from acute and chronic disease.
J Infect Dis., 162 (1990), pp. 695-699
[8]
J.J. Ferrara, J. Leveque, D.L. Dyess, C.O. Lorino.
Nonsurgical management of breast infections in nonlactating women. A word of caution.
Am Surg., 56 (1990), pp. 668-671
[9]
N.J. Bundred, M.S. Dover, S. Coley, J.M. Morrison.
Breast abscesses and cigarette smoking.
Br J Surg., 79 (1992), pp. 58-59
[10]
J.C. Alados, M. Perez, J. Fontes.
Bacteriology of non-puerperal breast abscesses.
Int J Gynaecol Obstet., 48 (1995), pp. 105-106
[11]
C.M. Casas, M. Pérez, J.C. Alados, J. Fontes, G. Orellana, J.M. Aguilar, et al.
Nonpuerperal breast infection.
Infect Dis Obstet Gynecol., 3 (1995), pp. 64-66
[12]
F.N.L. Versluijs-Ossewaarde, R.M.H. Roumen, R.J.A. Goris.
Subareolar breast abscesses: characteristics and results of surgical treatment.
[13]
A. Moazzez, R.L. Kelso, S. Towfigh, H. Sohn, T.V. Berne, R.J. Mason.
Breast abscess bacteriologic features in the era of community-acquired methicillin-resistant Staphylococcus aureus epidemics.
Arch Surg., 142 (2007), pp. 881-884
[14]
A. Bharat, F. Gao, R.L. Aft, W.E. Gillanders, T.J. Eberlein, J.A. Margenthaler.
Predictors of primary breast abscesses and recurrence.
World J Surg., 33 (2009), pp. 2582-2586
[15]
N. Dabbas, M. Chand, A. Pallett, G.T. Royle, R. Sainsbury.
Have the organisms that cause breast abscess changed with time?—Implications for appropriate antibiotic usage in primary and secondary care.
Breast J., 16 (2010), pp. 412-415
[16]
K. Al Benwan, A. Al Mulla, V.O. Rotimi.
A study of the microbiology of breast abscess in a teaching hospital in Kuwait.
Med Princ Pract., 20 (2011), pp. 422-426
[17]
M. David, P. Handa, M. Castaldi.
Predictors of outcomes in managing breast abscesses—a large retrospective single-center analysis.
Breast J., 24 (2018), pp. 755-763
[18]
A. Saboo, I. Bennett.
Trends in non-lactational breast abscesses in a tertiary hospital setting.
ANZ J Surg., 88 (2018), pp. 739-744
[19]
C. O´Brien, E. Quinn, M. Murphy, E. Lehane, D.P. O´Leary, V. Livingstone, et al.
Breast abscess: not just a puerperal problem.
Breast J., 26 (2020), pp. 339-342
[20]
S.P. Russell, C. Neary, S. Abd Elwahab, J. Powell, N. O´Connell, L. Power, et al.
Breast infections—microbiology and treatment in an era of antibiotic resistance.
[21]
K.L. Frank, J.L. del Pozo, R. Patel.
From clinical microbiology to infection pathogenesis: how daring to be different works for Staphylococcus lugdunensis.
Clin Microbiol Rev., 21 (2008), pp. 111-133
[22]
N. Saraiya, M. Corpuz.
Corynebacterium kroppenstedtii: a challenging culprit in breast abscesses and granulomatous mastitis.
Curr Opin Obstet Gynecol., 31 (2019), pp. 325-332
[23]
S.M. Leal Jr., M. Jones, P.H. Gilligan.
Clinical significance of commensal Gram-positive rods routinely isolated from patient samples.
J Clin Microbiol., 54 (2016), pp. 2928-2936
[24]
F. Cobo, V. Guillot, J.M. Navarro-Marí.
Breast abscesses caused by anaerobic microorganisms: clinical and microbiological characteristics.
Antibiotics (Basel)., 9 (2020), pp. 341
[25]
S. Surani, H. Chandna, R.A. Weinstein.
Breast abscess: coagulase-negative Staphylococcus as a sole pathogen.
Clin Infect Dis., 17 (1993), pp. 701-704

Please cite this article as: Bartolomé-Álvarez J, Solves-Ferriz V. Microbiología de los abscesos mamarios. Enferm Infecc Microbiol Clin. 2022;40:479–482.

Copyright © 2021. Sociedad Española de Enfermedades Infecciosas y Microbiología Clínica
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