A 40-year-old Caucasian man presented to the dermatology clinic at Baylor College of Medicine, Houston, Texas, in February 2003, for the evaluation of three nonhealing
ulcers. The patient's past medical history was significant for
hypothyroidism and
pulmonary sarcoidosis, the diagnosis of which was made in June 2000. In March 2000, the patient had complained of
cough and
shortness of breath. A purified
protein derivative (
PPD) (Mantoux text) was negative. Computed tomography (CT) scans of the chest revealed diffuse hilar and mediastinal
adenopathy and bilateral interstitial and alveolar infiltrates. Although consistent with
sarcoidosis, these findings were insufficient to exclude other etiologies, including
disseminated fungal infection. Cultures and stains of subsequent bronchoscopy specimens failed to reveal any organisms, and histopathologic evaluation of the specimens was nondiagnostic. Based on the imaging studies and the negative cultures, a diagnosis of
sarcoidosis was made, and the patient was started on
therapy with
prednisone. Before coming to our clinic, the patient had been on several courses of
prednisone. In May 2002, the patient had presented to a private dermatologist with a 1-year history of a nonhealing 2.4 cm x 2.0 cm
ulcer on the left medial forearm. Two biopsies were reported as nondiagnostic. The patient's presentation was interpreted as most consistent with
Mycobacterium marinum infection, and so he was empirically treated with
minocycline. This treatment was continued for almost 3 months without improvement in the
ulcer. A few months after the
minocycline had been discontinued, the patient was treated empirically for 2 months with
ciprofloxacin. This treatment was also unsuccessful in ameliorating the
ulcer. In between the two courses of
antibiotics, specimens from the lesion were sent for bacterial and fungal cultures, which revealed normal skin flora. In January 2003, the patient returned to his private dermatologist with three ulcerations. In addition to the nonhealing
ulcer on his left forearm, which he had acquired several months earlier, he had also developed a 3.0 cm
ulcer on his right arm and a 3.0 cm
ulcer on his central back. The patient refused biopsies at this visit. Given the patient's previous diagnosis of
pulmonary sarcoidosis, it was thought that the skin lesions might represent ulcerative cutaneous
sarcoidosis.
Pyoderma gangrenosum was also considered to be a likely diagnosis. Therefore, the patient was started on a course of oral
prednisone, an effective
therapy for both
sarcoidosis and
pyoderma gangrenosum. Despite 1 month of treatment with 60 mg/day of
prednisone, the
ulcers increased, and the patient was subsequently referred to our clinic. Physical examination at the time of presentation revealed
steroid acne on the trunk and upper extremities and three non-tender
ulcers with erythematous, undermined borders (Figs 1-3). On the left arm, there was an adjacent nodule which the patient attributed to a
scar from a previously healed
ulcer. Histologic examination of biopsy specimens from all three sites showed similar findings. The lesion contained diffuse, suppurative, granulomatous, inflammatory infiltrates with extensive central
necrosis. The infiltrates were composed of histiocytes, multinucleated foreign-body-type giant cells, plasma cells, lymphocytes, neutrophils, and neutrophil fragments. No organisms were seen in the initial, routinely stained sections. However,
periodic acid-Schiff (PAS) staining demonstrated small fungal spores (Fig. 4) morphologically consistent with
sporotrichosis, within the cytoplasm of multinucleated histiocytic giant cells (Fig. 5). Additional stains for bacteria and
acid-fast organisms were negative. Cultures of the biopsy specimens from all three sites grew Sporothrix schenckii. Further questioning of the patient failed to reveal an obvious source of the
infection. The patient denied any history of traumatic skin inoculation and did not engage in gardening or other outdoor activities that are classically associated with
sporotrichosis. The patient did admit to blackberry picking on detailed retrospective questioning. Once the diagnosis of
sporotrichosis was made, the patient was given 200 mg/day of
itraconazole. After 2 months, the patient's
ulcers were almost completely healed. The patient's pulmonary complaints were also much improved.