Author/Authors :
Sanaei Dashti, Anahita Pediatric Infection Research Center (PIRC) - Mofid Children Hospital - Shaheed Beheshti University of Medical Sciences - Tehr , Sadeghi, Esmaeel Pediatric Infectious Diseases - Nemazee Hospital , Vijayananda Kumar, Perikala 3Department of Pathologist - Shaheed Faghihi Hospital, Shiraz University of Medical Sciences - Shiraz,
Abstract :
Acute neutrophilic dermatosis, first described in 1964 by
Robert Douglas Sweet, is characterized by sudden onset fever,
neutrophilic leukocytosis, and well demarcated erythematous
papules, nodules, and plaques with dense neutrophilic infiltrates
on histologic evaluation.
Here is a report of a 7-year-old girl who presented with
high grade fever, and discrete erythematous papular skin eruptions,
which gradually increased in number and involved the
face, trunk, extremities, palms, soles, hard palate, and palatal
tonsils. The skin eruptions evolved to pustules and after coalescing
caused large crusted plaques, with mild tenderness but
without any pruritus. White blood cells were 36900/ml with
92% neutrophils. Skin biopsy test was compatible with acute
febrile neutrophilic dermatosis, so prednisolone (1 mg/kg/day)
was started that led to a rapid defervescence and significant
improvement of dermatosis. After a few days, the patient presented
with fever and arthritis of right elbow, both ankles, and
wrists, so she was re-admitted. She also developed bloody diarrhea
during the hospital stay. Colonoscopy and intestinal
biopsy were performed, which confirmed the diagnosis of ulcerative
colitis. Prednisolone, sulfasalazine, and naproxen
were prescribed. The fever and diarrhea stopped after a few
days and joint swelling decreased. She was discharged 2
weeks after the admission with a rather good general condition.
Inflammatory bowel disease can be one of the several
conditions accompanying sweet syndrome.