A 69-year-old patient presented with a tender, thickly crusted skin lesion of 1 week's duration. A bacterial culture swab taken from the underlying granular tissue yielded a pure isolate of a Gram-negative coccobacillus, presumptively identified as a novel Francisella species via 16S rRNA and multilocus gene sequence analysis.
CASE REPORTO n 5 January 2011, a 69-year-old white male presented to a dermatology clinic with a tender lesion on his left ankle. The patient had been well until the previous week when he cut down an Arizona ash tree near his home in southern Louisiana, close to the Mississippi River. Branches from the tree scratched his legs and abraded his left ankle. He applied mupirocin ointment to the ankle lesion, but it became increasingly tender and erythematous. His underlying medical conditions included non-insulin-dependent diabetes, hypertension, hyperlipidemia, and a history of a squamous cell carcinoma excised from his right arm in March 2010. The patient denied fever, chills, or other systemic symptoms.On initial examination, the patient was afebrile with a 4-by 6-cm thickly crusted erythematous nodule on the medial aspect of the left ankle, with surrounding erythema and tenderness to palpation (Fig. 1A). Incision and drainage of the nodule was attempted; however, no pus or purulent drainage was noted. Tissue underlying the eschar was pink and granular. A biopsy specimen of the underlying granular tissue was submitted for histopathology, deep fungal culture, and atypical mycobacterial culture; a swab was also taken for routine bacterial culture.Initial histopathology of the biopsied tissue was interpreted as squamous cell carcinoma. The patient was referred to a general surgeon for excision of the lesion but, because of the surrounding erythema, was also prescribed 500 mg ciprofloxacin twice daily (BID) for 7 days. The patient noted improvement in the lesion after 24 h. Deep fungal and atypical mycobacterial cultures were both negative. A Gram-negative coccobacillus grew from the bacterial swab taken from the underlying granular tissue and was presumptively identified as Francisella tularensis (described below). Based on the isolation of a Francisella species from the lesion, an additional 7 days of ciprofloxacin was prescribed, and the pathologist who performed histopathology was contacted to review the initial biopsy specimen. The pathologist's amended report noted probable pseudoepitheliomatous hyperplasia overlying a dense suppurative granulomatous dermatitis, rather than squamous cell carcinoma. However, significant atypia was noted, and the remaining lesion was excised in the operating room on 4 March 2011. The area healed well without further sequelae. Subsequent independent histopathology of the biopsy tissue similarly indicated no evidence of squamous cell carcinoma but rather marked inflammation and pseudoepitheliomatous epidermal hyperplasia with a dense, mixed dermal infiltrate including scattered small neutrophilic microabscesses, histiocytes, lymphocytes, and plasma cells (Fig....