REPORT OF A CASE An 18-year-old white man was admitted to the Internal Medicine Service with a 9-day history of abdominal cramps, nausea, vomiting, bloody diarrhea, and a pruritic, papular rash over his extremities. Seven days before admission, he was treated empirically with amoxicillin. The rash improved, but 2 days before admission, the patient experienced migratory arthralgias and myalgias and a nonpruritic, purpuric eruption on his extremities. The day before admission, his medication was switched from amoxicillin to erythromycin. A review of his systems revealed no recent upper respiratory tract infections or fevers. On admission, the patient had a low-grade fever (temperature, 41.1°C), a pulse rate of 93/min, and a blood pressure reading of 112/46 mm Hg. A stool sample was guaiac positive. Skin examination revealed palpable purpuric lesions on the lower part of both legs ( Figure 1 ). There was also mild involvement of the forearms, but the palms and
[1]
Fauci As,et al.
Vasculitic syndromes.
,
1994,
Current opinion in rheumatology.
[2]
K. Danno,et al.
Successful treatment of adult Henoch-Schönlein purpura with factor XIII concentrate.
,
1991,
Journal of the American Academy of Dermatology.
[3]
N. Rosenblum,et al.
Steroid effects on the course of abdominal pain in children with Henoch-Schonlein purpura.
,
1987,
Pediatrics.
[4]
S. Green,et al.
The Koebner phenomenon in anaphylactoid purpura.
,
1986,
Cutis.
[5]
R. Hené,et al.
The relevance of IgA deposits in vessel walls of clinically normal skin. A prospective study.
,
1986,
Archives of internal medicine.
[6]
C. Wheeler,et al.
Urticarial Vasculitis: Report of a Case and Review of the Literature
,
1979
.