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Aeromonas sobria necrotizing fasciitis and sepsis in an immunocompromised patient: a case report and review of the literature

  • Savino Spadaro1Email author,
  • Angela Berselli1,
  • Elisabetta Marangoni1,
  • Anna Romanello1,
  • Maria Vittoria Colamussi1,
  • Riccardo Ragazzi1,
  • Silvia Zardi1 and
  • Carlo Alberto Volta1
Journal of Medical Case Reports20148:315

https://doi.org/10.1186/1752-1947-8-315

Received: 5 April 2014

Accepted: 24 July 2014

Published: 22 September 2014

Abstract

Introduction

Aeromonas veronii biovar sobria is a rare cause of bacteremia, with several studies indicating that this isolate may be of particular clinical significance since it is enterotoxin producing. A wide spectrum of infections has been associated with Aeromonas species in developing countries that include gastroenteritis, wound infections, septicemia and lung infections. This infection, caused by Aeromonas species, is usually more severe in immunocompromised than immunocompetent individuals. We here describe a case of soft tissue infection and severe sepsis due to Aeromonas sobria in an immunocompromised patient.

Case presentation

A 74-year-old Caucasian man with a clinical history of chronic lymphocytic leukemia and immune thrombocytopenia, periodically treated with steroids, was admitted to our Intensive Care Unit because of necrotizing fasciitis and multiorgan failure due to Aeromonas sobria, which resulted in his death. The unfortunate coexistence of a Candida albicans infection played a key role in the clinical course.

Conclusion

Our experience suggests that early recognition and aggressive medical and surgical therapy are determinants in the treatment of severe septicemia caused by an Aeromonas sobria in an immunocompromised patient.

Keywords

Aeromonas sobria Immunocompromised hostNecrotizing fasciitisSepsis

Introduction

Necrotizing fasciitis is a destructive soft tissue infection characterized by an extensive necrosis in skin, subcutaneous tissues and fascia that is associated with systemic toxicity and fulminant course with a mortality rate varying from 40% to 60%[1]. Immunosuppression, diabetes mellitus, alcoholism, end-stage renal disease, malignancy and chemotherapy have all been suggested as predisposing factors in necrotizing fasciitis[2].

Bacteria associated with necrotizing fasciitis include Aeromonas species[3]. Aeromonas organisms are Gram-negative small bacilli isolated from a variety of environmental sources including water, seafood, meat and vegetables, with the ability to colonize both humans and animals[4]. The clinical spectrum of Aeromonas species infection in humans includes acute gastroenteritis, hepatobiliary tract infection, pneumonia, empyema, meningitis, septic arthritis, osteomyelitis, endocarditis, bacteremia, burn and wound infection[5, 6].

Clinical isolates in 85% of human infections involve three phenotypically defined species: Aeromonas hydrophila, Aeromonas caviae and Aeromonas veronii biovar sobria[7]. A. veronii biovar sobria is predominantly isolated in patient’s blood and is more pathogenic than A. hydrophila[7, 8]. The possible portals of entry for Aeromonas bacteremia are gastrointestinal tracts, skin lesions, previous surgery or local trauma in an aqueous environment[9]. After adhesion to epithelial cells, Aeromonas produces many virulent factors which destroy host epithelial barriers and impair immune cells, including exoenzymes, cytotoxic and cytotonic enterotoxins, hemolysins, proteinases, lipases, agglutinins, various hydrolytic enzymes, translocation capacity and a Aeromonas sobria cytotoxic factor[4, 10, 11]. Aeromonas infections can develop in healthy and trauma patients, but immunocompromised hosts with hematologic malignancy, cancer and hepatobiliary diseases are considered to be at greatest risk[12]. Patients with severe wound infection (myonecrosis) caused by this microorganism also develop sepsis, and 90% of patients succumb to their infections[13]. The fatality rate of Aeromonas soft tissue infections and bacteremia is high and reportedly ranges from as much as 28% to 73%, with septic shock being the cause of death in the majority of patients[14].

Case presentation

We present the case of a 74-year-old Caucasian man with a medical history of ischemic heart disease, atrial flutter, arterial hypertension, severe aortic stenosis, chronic lymphocytic leukemia and related immune thrombocytopenia periodically treated with steroids (every 28 days). He was referred to our Emergency Room for fever and an altered state of consciousness. During the clinical examination, his temperature was 40°C, his blood pressure was 120/80mmHg, pulse 89 beats per minute, arrhythmic and his initial oxygen saturation checked by pulse oximetry was 95% in room air. He was somnolent but easily aroused and on examination presented pulmonary bibasal crepitations, heart murmur and a hematoma on his left foot. A laboratory evaluation revealed an increase in white blood cell (WBC) count (15.0×103/μL; reference value 4.00 to 11.00×103/μL), platelet count of 56×103 cells/μL (reference value 150 to 450×103 cells/μL), and C-reactive protein 6.6mg/dL (reference value 0.0 to 0.5mg/dL). Four days before hospital admission, while fishing, his left hand had been scratched by the dorsal fin spine of a black bullhead (Ameiurus melas, catfish); no physical signs in situ were present on initial examination. He was hospitalized in the Clinic of Infectious Diseases, Ferrara. On admission, an empiric antibiotic treatment with ampicillin-sulbactam (3g every 8 hours, intravenous) was initiated intravenously; blood cultures were performed. The day after admission, his vital signs and body temperature were normal but he began to complain of muscle weakness and of severe pain in his lower extremities, radiating to his knees. A neurological examination revealed an asymmetric hyposthenia and hypoesthesia of his lower limbs, bilateral areflexia of his Achilles tendon, lower extremity acute paresis, and bladder dysfunction. A spine magnetic resonance imaging excluded cauda equina syndrome, while the vascular surgeon excluded an acute ischemic peripheral event. To exclude endocarditis an echocardiography was performed, revealing a global cardiac contractile dysfunction with a severe reduction in ejection fraction (35%). Antibiotic therapy was changed to ceftriaxone (2g every 24 hours, intravenous) and levofloxacin (500mg every 12 hours, intravenous) because of the further increase in his WBC count (24.3×103 cells/mm3), and blood cultures revealed an increase in Gram-negative bacilli that were later confirmed to be A. sobria, the latter being identified by Vitek® II method.

After 48 hours, his clinical condition deteriorated and he developed severe sepsis with hypotension (systolic blood pressure was 80mmHg) and peripheral vasoconstriction, acute renal failure with oliguria (urea: 159mg/dL and creatinine: 2.55mg/dL), and severe metabolic acidosis. He was therefore transferred to our Intensive Care Unit (ICU). At this time, laboratory values were as follows: WBC count of 17.4×103 cells/mm3, platelet count of 38×103 cells/mm3, procalcitonin 99.3ng/mL (reference value <0.05ng/mL), and C-reactive protein 46.9mg/dL (reference value 0 to 0.5mg/dL). An antimicrobial regimen was promptly implemented with meropenem (1g every 12 hours, intravenous) and linezolid (600mg every 12 hours, intravenous). Laboratory data suggested a diagnosis of rhabdomyolysis (creatinine phosphinase 5013U/L; reference value <190U/L), myoglobinemia 13270ng/mL (reference value 28 to 72ng/mL), lactate dehydrogenase 673U/L (reference value 240 to 480U/L) and, on physical examination, his lower limbs were warm in presence of erythema. After 12 hours, the swelling of his legs and progression of skin lesions (circumferential erythema developed in bullae formations) increased until a compartment syndrome developed, rapidly requiring surgical treatment with bilateral fasciotomy (Figures 1 and2).
Figure 1

Early skin lesions of lower limbs before fasciotomy.

Figure 2

Gangrenous lower limbs after fasciotomy.

Blood culture results were available 3 days after ICU admission. The strain was identified as Aeromonas sobria. The isolate was susceptible to amikacin, cefepime, cefotaxime, ceftazidime, levofloxacin, ertapenem, gentamicin, and piperacillin-tazobactam. Resistance to meropenem and imipenem were also observed. Antibiotics were adjusted in relation to blood culture and sensitivities. Consequently, meropenem was discontinued and he was given ceftazidime (2g every 8 hours, intravenous).

On ICU day 7, due to return of spiking fever and leg pain, computed tomography (CT) scans were performed. CT scans of his lower extremities showed progression to overt fasciitis with gaseous infiltration in the soft tissues (Figure 3). In view of the CT scan images and microbiological results, the surgeon was consulted and amputation for necrotizing infections of the extremities was performed. Deep wound cultures yielded growth of Gram-negative bacilli, which were identified as A. sobria. No anaerobes were detected from necrotic tissue. After surgical and medical treatment, his clinical status showed progressive improvement in renal, cardiocirculatory, splanchnic and metabolic function. Laboratory findings revealed no further signs of rhabdomyolysis (creatinine phosphinase 97U/L, lactate dehydrogenase 378U/L); a progressive reduction in WBC count (13.7×103 cells/mm3), a platelet count of 122×103 cells/mm3, procalcitonin 0.88ng/mL, urea 58mg/dL and creatinine 0.78mg/dL were observed. Over the course of weeks, consecutive blood cultures showed Aeromonas microorganisms were no longer isolated.
Figure 3

Computed tomography scans of legs demonstrating gas gangrene.

Although surgical wounds following bilateral amputation presented no further signs of necrosis, frequent surgical debridements were still necessary. In order to perform these painful procedures he was heavily sedated and required mechanical ventilation, which prolonged his stay in the ICU. Despite the aggressive treatment and administration of broad-spectrum antibiotics, including antifungal prophylaxis, the coexistence of immunocompromised host and comorbidities induced during his ICU stay, caused the development of an invasive candidemia (Candida albicans) which was ultimately responsible for his death.

Discussion

The clinical manifestations and outcomes of Aeromonas-associated soft tissue infections vary in relation to the immune status of the host. Since Aeromonas species were considered rare pathogens of necrotizing fasciitis in immunocompromised patients[11, 12], we present an uncommon case of A. sobria necrotizing fasciitis in Italy. In immunocompromised hosts, Aeromonas-associated soft tissue infections can be fulminant and fatal. Previous studies have shown that Aeromonas species infections are strongly associated with mortality[15]. Table 1 shows cases of Aeromonas species necrotizing fasciitis that have been reported in the literature. Similar features are revealed in the literature and previously described case reports have comparable clinical characteristics. Chang et al.[6] illustrated a fulminant necrotizing fasciitis caused by A. sobria in patients with neutropenia whose fatal clinical course was just like that described by Martino et al.[9] in their report of two cases with acute non-lymphoblastic leukemia who developed septic shock caused by Aeromonas species with soft tissue complications. Both studies confirm the potentially aggressive nature of these bacteria in patients with neutropenic cancer. Tsai et al.[14] also reported the rapid onset of skin necrosis and sepsis caused by A. sobria in two patients with diabetes who died only a few days after admission. Finally, Stano et al.[4] described a fatal A. sobria sepsis complicated by rhabdomyolysis in a patient with human immunodeficiency virus. What is described in the literature seems to suggest that A. sobria is the more pathogenic among Aeromonas bacteria since only patients with infections caused by A. hydrophila survived[9].
Table 1

Cases of necrotizing fasciitis caused by Aeromonas species reported in the medical literature

Cases

Gender/age (year)

Predisposing factors

Location

Species

Antibiotics

Surgical treatments

Outcome/length of stay (days)

Chang et al.[6]

M/60

B-cell acute lymphoblastic leukemia

Lower extremities

Aeromonas sobria

Ceftazidime+teicoplanin

None

Death/7

→imipenem/cilastatin+vancomycin

 

F/39

T-lineage acute lymphoblastic leukemia

Lower extremities

A. sobria

Imipenem/cilastatin→levofloxacin

None

Death/3

 

M/65

Acute myeloid leukemia

Lower extremities

A. sobria

Ceftazidime+teicoplanin

None

Death/5

Tsai et al.[14]

M/66

Diabetes mellitus, local wound trauma

Forearm

A. sobria

Cefuroxime+gentamicin

Fasciotomy+debridement

Death/2

 

M/79

Diabetes mellitus

Lower extremities

A. sobria

Vancomycin+ceftazidime

Amputation

Death/11

→ceftriaxone+metronidazole

Stano et al.[4]

M/43

Human immunodeficiency virus and hepatitis C virus infected

Lower extremities (rhabdomyolysis)

A. sobria

Metronidazole+ceftriaxone

None

Death/-

Martino et al.[9]

F/41

Acute non-lymphoblastic leukemia

Calf (local myonecrosis and pseudoabscess)

Aeromonas hydrophila

Ceftazidime+amikacin+ciprofloxacin

Drainage

Cured

 

M/50

Acute non-lymphoblastic leukemia

Lower extremities

A. sobria

Ceftazidime+amikacin

None

Death/3

Kao et al.[16]

M/76

Local trauma

Hand

Aeromonas schubertii

Penicillin→minocycline

Fasciotomy+debridement

Death/-

Furusu et al.[17]

M/66

Diabetes mellitus, liver dysfunction, hemodialysed

Lower extremity

A. hydrophila

Piperacillin+clindamycin

Fasciotomy+debridement→amputation

Cured

→clindamycin+minocycline

+ceftazidime

→aztreonam+clindamycin

Apisarnthanarak et al.[18]

M/61

Cirrhosis

Neck soft tissue

A. hydrophila

Amoxicillin→ampicillin-clavulanate→ceftriaxone

Debridement

Cured

+clindamycin+ciprofloxacin

Minnaganti et al.[1]

M/81

Congestive heart failure and peripheral neuropathy

Forearm

A. hydrophila

Clindamycin+Levofloxacin

Amputation

Death/-

Kumar et al.[19]

M/71

Hypertension and previous coronary artery bypass graft

Lower extremity

Aeromonas caviae

Ceftriaxone+amikacin

Fasciotomy+debridement

Cured

M, male; F, female.

Two mechanisms have been proposed to explain the onset of Aeromonas soft tissue skin infection. The first mechanism postulates that the bacterium invades through trauma, triggering primary infection of the soft tissue causing subsequent development of sepsis. According to the second mechanism, sepsis is first induced by the pathogen and then by metastatic lesions in the soft tissue[11]. In patients with bacteremia, the source of bacteremia is often unclear. A review reported that Aeromonas species are causative organisms more commonly found in those who are exposed to seawater or raw seafood, making fisherman an occupation group at higher risk[3].

The ability of Aeromonas to cause disease is affected not only by patient characteristics but also microbial factors, and the products of the organisms are responsible for hypotension, multiorgan failure, and disseminated intravascular coagulation, which may lead to septic shock as a result of vascular leakage and vasodilatation[3].

A. sobria is a human pathogen; the cases of bacterial infections described refer to healthy subjects affected with gastrointestinal infection[10]. However, patients with severe wound infection caused by A. sobria also develop sepsis and >90% of the patients succumb to their infections; published data have shown that a serine proteinase secreted by A. sobria, at infection sites or in the circulation, points to a mechanism of virulence that could be associated with the induction of septic shock caused by infection with this bacterium[10].

Although Aeromonas has a propensity to produce at least three β-lactamases, these microorganisms are generally susceptible to the majority of antibiotics active against Gram-negative bacilli. This notwithstanding, increasing antimicrobial resistance among Aeromonas species has been observed depending mainly on species, source and country of isolation[4, 5]. Some authors recommend obtaining a susceptibility test before deciding the correct treatment regime and delaying proper antibiotics until culture results are available. This delay, however, may endanger patients, especially neutropenic patients[4, 6]. After evaluating monomicrobial Aeromonas, Ko and Chuang did not observe any major differences in treatment with a combination of aminoglycoside and β-lactam, and they suggested that a broad-spectrum cephalosporin remains one of the main therapeutic choices in invasive Aeromonas infections[5].

The two most common pitfalls in management of Aeromonas necrotizing fasciitis are the failure to make an early diagnosis and inadequate medical and surgical treatment[6]. The literature reports that early surgical intervention is essential in immunocompromised hosts with this infection[9] and that more aggressive early surgical intervention may be indicated in these patients[14].

In the present case, all predisposing factors for a typical Aeromonas infection were present; our patient had a clinical history of hematological disorders and infection was most likely caused by exposure of a wound to contaminated water (the patient had immersed his hands into potentially contaminated water while fishing and was scratched by a catfish). Nevertheless, some aspects contributed to failure of the case. The lack of any clear clinical signs and symptoms prevented early diagnosis. It is crucial to remember that pain which appears to be disproportional to the physical findings is the most consistent manifestation of necrotizing fasciitis, and that the presence of bullae also constitutes an important diagnostic clue. It is suggested in the literature that these two aspects should be taken into account since the earlier necrotizing fasciitis is diagnosed, the better the outcome and the fewer the complications[12]. During the first 36 hours spent in our Medical Department, our patient mainly presented pain and motor disability, making it difficult for the clinicians to formulate a correct diagnosis.

Furthermore, clinical differentiation between Aeromonas necrotizing fasciitis and infections caused by other microorganisms is no easy matter. In the case of gas-producing muscular necrosis, as in our patient, an infection of possible Clostridium origin should be taken into consideration[15]. In the case of lesions where neither Gram-positive nor anaerobic bacilli are detected, Aeromonas ought to be suspected, just as the need to deliver prompt and appropriate empiric antibiotic therapy and aggressive surgical treatment should be considered. Concurrent immunosuppression, consequent to the hematologic disease and the chronic use of steroids may, in our case, have contributed to the pathogenesis and virulence of the Aeromonas disease, as well as the unfortunate coexistence of fungal infection which played a key role in the clinical course.

Conclusions

This is a report of an uncommon case of Aeromonas sobria sepsis in an immunocompromised patient. We reviewed the literature and found that the presentation, treatment and final resolution of this case is consistent with the data presented in the literature.

It is, therefore, important for physicians caring for immunocompromised patients with necrotizing fasciitis to consider the possible involvement of Aeromonas species as the causative agent of infection. Time is a critical element in the treatment of immunocompromised patients presenting a rapid onset of skin necrosis and progressive sepsis. Early recognition and aggressive medical and surgical therapy are the primary determinants of outcome in the treatment of these patients.

Consent

Informed written consent was obtained from the patient’s next of kin for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Abbreviations

CT: 

Computed tomography

ICU: 

Intensive care unit

WBC: 

White blood cell.

Declarations

Authors’ Affiliations

(1)
Department of Morphology, Surgery and Experimental Medicine, Sant’ Anna Hospital, University of Ferrara

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© Spadaro et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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