STRONGYLOIDES stercoralis, an intestinal nematode commonly known as the human threadworm, affects an estimated 34 million people in the world.1 Chronic infection is often asymptomatic and may persist for many years after the normal host has left an endemic area. Immunocompromised patients may develop a fulminant illness due to a unique process in the life cycle of S stercoralis in which there are dramatic increases in the number of filariform (infective) larvae.The association between disseminated strongyloidiasis and immunosuppression was first noted in 19662-4 and has been well confirmed since then.We describe a patient with fatal disseminated strongyloidiasis who developed a periumbilical purpuric eruption in which S stercoralis larvae were found on antemortem skin biopsy specimens. We believe this is the first case of widespread skin involvement in disseminated strongyloidiasis.
Report of a CaseA 62-year-old woman was admitted to Columbia Presbyterian Medical Center, New York, because of fever and abdominal pain. She was born in the Dominican Republic but had lived in the United States for ten years. Polymyositis was diagnosed elsewhere by muscle biopsy and she was treated with oral corticosteroids (prednisone, 80 mg/d, alternating with 60 mg/d).One week prior to admission to the medical center she was evaluated at another hospital; she had a tempera¬ ture of 38.9°C, midepigastric pain, and a white blood cell (WBC) count of 7300/mm3 (7.3X10VL) with 48% (0.48) polymorphonuclear leukocytes and 27% (0.27) band forms. Results of a barium enema examination and an upper gastrointestinal tract series were normal. She signed out of the hospital against medical advice when an explor¬ atory laparotomy was recommended.At the time of admission to the hospital, she was acutely ill with a temperature of 38.1°C, tachypnea, and tachycardia. She had diffuse abdomi¬ nal tenderness without rebound, dimin¬ ished bowel sounds, and end-expiratory wheezes. No skin eruption was noted. Laboratory data were significant for a WBC count of 18 900/mm3 (18.9X107 L) with 78% (0.78) polymorphonuclear leukocytes, 11% (0.11) band forms, 2% (0.2) metamyelocytes, and 1% (0.1) myelocytes. She never demonstrated eosinophilia during her hospital course. A chest roentgenogram showed bilater¬ al interstitial lung disease. Abdominal roentgenograms showed air in nondistended largeand small-bowel loops, with no evidence of obstruction. Perito¬ neal lavage on the day of admission did not reveal free blood. She was treated for sepsis from a probable intraabdominal source with cefoxitin sodi¬ um and tobramycin sulfate. Her overall condition deteriorated. Her chest roentgenogram progressed to a reticulonodular pattern. Hypoxemia developed and she required in¬ tubation. Fiberoptic bronchoscopy demonstrated acute tracheobronchial inflammation. Sulfamethoxazole-trimethoprim therapy was started. Re¬ sults of emergency laparoscopy on the second hospital day were normal. Com¬ puted tomographic scans of the abdo¬ men and pelvis were normal. On the third hospital...