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Case In Point
An Intriguing Diagnosis 

Stevens-Johnson Syndrome

By HELENE TIGCHELAAR, MD, NIRUPAMA KANNIKESWARAN, MD, and DEEPAK KAMAT, MD, PhD | December 1, 2008
Children’s Hospital of Michigan, Wayne State University
Dr Tigchelaar is clinical associate professor of pediatrics and staff physician in the emergency department and Dr Kannikeswaran is assistant professor of pediatrics at the Children’s Hospital of Michigan in Detroit. Dr Kamat is professor of pediatrics at Wayne State University in Detroit; and vice chair of education and Director of the Institute of MedicalEducation in The Carman and Ann Adams Department of Pediatrics at the Children’s Hospital of Michigan.

A 13-year-old boy was brought to the emergency department (ED) with a generalized itchy rash of 2 days' duration. For the past 3 days, he had dry, itchy eyes with a purulent discharge (Figure 1) and nonbilious emesis 2 or 3 times per day, with some blood streaks in the vomitus on the third day of illness. Chills developed on the third day, but the patient's temperature was not measured. His lips were swollen and cracked (Figure 2), which made it painful to eat or drink. About 6 months earlier, he had a similar episode that resolved with application of a topical cream to the lips. He also had painful urination without urgency or penile discharge. He denied recent use of medications and had no ill family members. He had been well before the onset of symptoms.

 


Figure 1 – About 30% of children with Stevens-Johnson syndrome have ocular involvement. This 13-year-old boy had mucopurulent conjunctivitis with episcleritis as a manifestation of the disease.
(MORE: Toxic Epidermal Necrolysis Secondary to Anticonvulsant Medication)

 

 


Figure 2 – Mucositis of the lips in this teenager was a manifestation of Stevens-Johnson syndrome. Oral lesions are the most common type of mucosal involvement in affected patients. They are extremely painful and limit oral intake.

 

The teenager was apathetic, mildly dehydrated, and appeared to be in pain. Oral temperature was 39.6ºC (103.2ºF); respiration rate, 20 breaths per minute; heart rate, 108 beats per minute; and blood pressure, 108/63 mm Hg. Physical examination revealed injection of the conjunctivae with sticky yellow discharge, swollen lips with erosion of the mucosa, hemorrhagic crusting, intraoral ulcers, dry oral mucous membranes, ulceration of the head of the penis, and a generalized rash that consisted of target lesions with central erosions.

The white blood cell count was normal (6700/μL), without a left shift; hemoglobin level was 14.3 g/dL. Results of coagulation studies were normal. The erythrocyte sedimentation rate and C-reactive protein level were markedly elevated (107 mm/h and 33.78 mg/L, respectively). Serum electrolyte levels were normal, blood urea(Drug information on urea) nitrogen level was elevated (33 mg/dL), and creatinine level was 1.3 mg/dL. Liver function test results were normal; the albumin level was slightly below normal (3.3 g/dL). Urinalysis results showed a specific gravity of 1.028 and 1+ protein; all other parameters were within normal range. IgA was 183 mg/dL. Direct fluorescent antibody studies of lip vesicles for herpes simplex virus types 1 and 2 were negative. Fluorescein(Drug information on fluorescein) examination of the eye demonstrated no corneal uptake of dye. A blood sample for culture was obtained.

In the ED, the patient received intravenous saline, ceftriaxone(Drug information on ceftriaxone) (a single dose), acyclovir, diphenhydramine(Drug information on diphenhydramine), and analgesia. A topical analgesic was applied to the ulcerated mouth, and emollients were applied to the rash. The ophthalmology consultant diagnosed mucopurulent conjunctivitis with episcleritis and recommended lubrication with artificial tears and erythromycin(Drug information on erythromycin) ophthalmic ointment. The dermatology consultant performed a biopsy of a target lesion, which demonstrated interface dermatitis with vacuolation of the basal layer and rare dyskeratotic cells in the epidermis suggestive of Stevens- Johnson syndrome (SJS) or erythema multiforme (EM).

Serological test results were negative for Mycoplasma; herpes simplex virus; Epstein-Barr virus; Cytomegalovirus; HIV; hepatitis A, B, and C viruses; and Treponema pallidum. Blood culture was negative.

Because of persistent vomiting and a steadily increasing elevated lipase level (from 713 U/L to a maximum of 1589 U/L), abdominal ultrasonography was performed. The size of the pancreas was at the upper limits of normal; there was a small amount of free fluid in the abdomen.

During the patient's 10-day hospitalization, intravenous hydration was maintained until he was able to tolerate oral feeds. At discharge, the eye and skin lesions had completely resolved and the oral ulcers had almost completely healed. The final diagnosis was SJS and acute pancreatitis.

(Discussion on next page.)


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