Superficial granulomatous pyoderma gangrenosum, a rare variant of pyoderma gangrenosum, has been considered to be the most benign form of the disease. We present the case of a 15-year-old boy with pulmonary involvement and nodular scleritis associated with this unusual type of pyoderma gangrenosum and discuss its differential diagnosis.
| CASE REPORTA 15-year-old boy presented with a pustular, warty eruption of 4 months duration. Cutaneous lesions involving the scalp, trunk, limbs, and genitals were characterized by numerous pustules surrounded by an erythematous halo and vegetative and keratotic plaques with crusts and purulent discharge overlying ulcerated, slightly painful plaques ( Figure 1A,B). Ocular examination showed erythema, conjunctival injection, and scleral nodules (Figure 2A). Several 2-to 3-mm pustules were seen on the hard palate. He also had marked digital clubbing and cyanosis ( Figure 2B), despite pulmonary auscultation with no remarkable findings, absence of dyspnea, and pulse oximetry of 92%.The patient's disease had started 9 months before with cough and he was treated for chronic bronchitis, with partial improvement.Five months before the onset of the dermatosis, he was empirically treated for pulmonary tuberculosis, but the cough persisted.During examination, a pathergy test was negative, and chest Xrays revealed a reticulonodular pattern and probable bronchiectases.Computed tomography (CT) showed pleural fibrosis, the vascular pattern was more apparent, and noncavitated nodules. Paranasal sinus CT was normal. Lung function tests showed a mild restrictive pattern. Bronchoscopy revealed mild tracheoendobronchitis with a diffuse nodular pattern. Tests were negative for microorganisms. Pulmonary hypertension was excluded. Complete blood cell count showed leukocytosis (12 9 10 3 /mm) with neutrophilia (77%). Erythrocyte sedimentation rate (22 mm/h) and C-reactive protein