Ecthyma gangrenosum without bacteremia in a previously healthy man: a case report
© Gençer et al; licensee BioMed Central Ltd. 2008
Received: 20 August 2007
Accepted: 22 January 2008
Published: 22 January 2008
Ecthyma gangrenosum is known as a characteristic lesion of Pseudomonas aeruginosa sepsis and is usually seen in immunocompromised patients.
A previously healthy 63-year-old man was admitted with sloughy necrotic ulcerations of the skin over his sternum. He was afebrile and in good condition. A skin biopsy revealed ecthyma gangrenosum. Blood cultures remained sterile, but a culture of biopsy material grew Pseudomonas aeruginosa.
Ecthyma gangrenosum may develop even in the absence of bacteremia and even in immunocompetent patients. It should be considered as a possible diagnosis even when a previously healthy patient has negative blood cultures.
Ecthyma gangrenosum is a characteristic necrotic and bullous skin lesion known to be caused by Pseudomonas aeruginosa sepsis. It is usually seen in immunocompromised people. However, it is rare to see ecthyma gangrenosum in people with no evidence of bacteremia [1–6] and in those who were previously healthy . Herein, we report a rare presentation of ecthyma gangrenosum in a previously healthy adult male without bacteremia.
A previously healthy 63-year-old man was admitted with a two week history of wounds over his sternum. Twenty days before hospital admission, he had developed fever and sore throat. Oral amoxicillin was given. Six days later he noted an erythematous skin lesion over his sternum. One week later his sore throat resolved but the skin lesion worsened. He presented to a dermatologist and was diagnosed with erysipelas and received oral amoxicillin again. Over the next two days, the skin lesion evolved to form vesicles that were drained in the emergency department of another hospital. The lesion progressed to ulceration over the next five days.
The patient had no history of immunosuppressive disease or treatment.
It is well known that ecthyma gangrenosum is one of the major dermatologic manifestations of severe, systemic Pseudomonas aeruginosa infection. It occurs in only 1–6% of patients with Pseudomonas bacteremia . It had been considered to be pathognomonic of Pseudomonas sepsis until it was described in cases with infections caused by group A Streptococcus, Aeromonas hydrophila, Staphylococcus aureus, Serratia marcescens, Pseudomonas maltophilia, Escherichia coli, Candida albicans, Aspergillus species and Mucor species .
Ecthyma gangrenosum is usually seen in immunocompromised patients with leukemia, lymphoma, other malignant diseases, severe burns or organ transplant, or in people receiving immunosuppressive therapy [1, 2, 4, 6]. However, it has been reported also in patients without previously identified medical problems. Most of them had a concurrent viral infection or had received recent antibiotic therapy . Ecthyma gangrenosum might be the first manifestation of an underlying medical problem and previously healthy patients should be followed closely in the future [7, 10].
The lesion begins as a painless red macule that enlarges and becomes a slightly elevated papule. It evolves to a hemorrhagic bulla that ruptures, forming a gangrenous ulcer with a gray-black eschar surrounded by an erythematous halo . Classically, the pathogen is isolated from the skin lesions as well as from the blood. These lesions may occur anywhere, but are most usual on the anogenital region, buttocks, extremities, abdomen, axillae and rarely on the face [1, 5].
Histologically, the lesions represent a necrotising vasculitis caused by direct bacterial invasion of the media and adventitia of the vascular walls, but not the intima . In general, acute mixed inflammatory cell infiltration and vascular proliferation are seen in the dermis, often involving the subcutaneous tissue. Elastases produced by Pseudomonas destroy the elastic small vessels, leading to hemorrhage and release of organisms into the surrounding tissue. Protease and endotoxin A elaborated by bacilli are responsible for the direct tissue destruction and ulcerative lesions. [5, 9].
In classic bacteremic ecthyma gangrenosum, the lesion represents a blood-borne metastatic seeding of Pseudomonas aeruginosa to the skin. However, there are a few reports that ecthyma gangrenosum can represent localized skin eruptions that are not accompanied by bacteremia or systemic infection [1–6].
The source of infection in this patient cannot be determined with certainty, but it is possible that the patient presented with erysipelas which subsequently became colonized and superinfected with hospital-acquired Pseudomonas aeruginosa while draining and then developed into ecthyma gangrenosum. Negative blood cultures suggest that ecthyma gangrenosum occurred as a primary lesion at a site of prior skin trauma.
Early diagnosis and aggressive therapy are important in the management of ecthyma gangrenosum. An antipseudomonal beta-lactam antibiotic with or without an aminoglycoside is appropriate for treatment of both bacteremic and nonbacteremic ecthyma gangrenosum . The absence of bacteremia is associated with the best outcome. Patients with Pseudomonas bacteremia have been reported to have a mortality rate of 38% . On the other hand, only two patients (15%) died in a review of 13 patients with ecthyma gangrenosum without bacteremia . In another study, the mortality rate was 7.5 % in the group of patients with skin lesions considered to be primary and 20 % in the group of patients with skin lesions considered to be secondary to bacteremia .
As we point out in this case, ecthyma gangrenosum may develop even in the absence of bacteremia and even in immunocompetent people. It may be treated with appropriate antibiotics upon diagnosis by tissue culture and microscopic examination. In conclusion, ecthyma gangrenosum should be considered as a possible diagnosis even when a previously healthy patient has negative blood cultures.
Written informed consent was obtained from the patient 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.
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