Group B streptococcal necrotizing fasciitis from a decubitus ulcer

A 29-year-old man with paraplegia secondary to a gunshot wound presented to the emergency department (ED) with worsening abdominal pain over the past 2 weeks with associated fever, dysuria, nausea, and vomiting. He had been diagnosed with a urinary tract infection (UTI) 2 days earlier and was started on antibiotics without improvement.

On examination he was afebrile, tachycardic up to 140, tachypneic, and diaphoretic. His abdomen was rigid and diffusely tender to palpation with hypoactive bowel sounds. He had a mildly tender 3 × 3 cm decubitus ulcer on his buttocks. His WBC was elevated at 18, with an absolute neutrophil count of 11.09 and 3.17 bands. The creatine kinase was elevated at 1,001 and a serum lactate level was 8.7. Abdominal computed tomography (CT) showed free air dissecting into the retroperitoneal and peritoneal fascial planes consistent with necrotizing fasciitis (Fig. 1, Fig. 2, Fig. 3, and Fig. 4).

Necrotizing fasciitis, more commonly known as the “flesh-eating disease,” is an aggressive and highly destructive infection of fascia and muscle with a high morbidity and mortality. Necrotizing fasciitis from decubitus ulcers is rare, with only a few reported cases [1, 2]. The diagnosis can be difficult, as symptoms are nonspecific and the initial skin lesions are often benign compared to the underlying tissue destruction [3]. A high index of suspicion should be present when abdominal radiographs demonstrate subcutaneous emphysema in a patient with skin lesions [4]. On CT, free air with evidence of soft tissue invasion is consistent with the diagnosis [2]. This case is unique because the decubitus ulcer and peritoneal samplings both grew and isolated group B streptococci as the causative agents; necrotizing fasciitis is typically caused by group A streptococci, Staphylococcus aureus, Vibrio vulnificus, Clostridium perfringens, Bacteroides fragilis, or mixed flora.