AOCD Homepage 

Main Index 
 
 Grand Round Cases
 2011 Academic Year
 2010 Academic Year
 2009 Academic Year
 2008 Academic Year
 2007 Academic Year
 2006 Academic Year
 2005 Academic Year
 2004 Academic Year
 2003 Academic Year
 2002 Academic Year
 
 Online Case Discussion
 
 Submission Guidelines
 
 Program Case Assignment
 
 Contact the Editors
 
 Online Case Discussion
Search

Grand Round Cases : 2010 Academic Year Last Updated: Oct 12th, 2010 - 01:53:47


Title: Rash in Hospitalized Patient
Presenter: Jonathan Richey, DO, Monica Nafsou, DO
Dermatology Program: Pontiac/Botsford Osteopathic Hospital
Program Director: Annette LaCasse, DO
Submitted on: Jul 2, 2010

Email this article
 Printer friendly page
CHIEF COMPLAINT:  "Red, painful rash on butt and armpits."

CLINICAL HISTORY:

Signs and symptoms:  A 44-year-old Caucasian male with a history of lower extremity osteomyelitis was treated with Unasyn and Vancomycin following below the knee amputation.

Previous Treatment: 

Other information:  The patient had no prior medical history, largely due to inadequate health maintenance. He had a 20-pack year history of smoking. On the eighth day of treatment with antibiotics after amputation, the patient developed a “rash.” The patient described the lesions as "very painful” - the worst areas being the right axilla and sacral area.

PHYSICAL EXAM:

Erythematous, erosive plaques and flaccid bullae on his buttocks. The right axillae, deltoid, chest and back had a morbilliform eruption and multiple 6-8 mm erythematous well-circumscribed plaques.

Day 1 Low Back


Day 1 Upper Back: Notice bullae in right axillae


Day 1 Right Axilla


Day 2 Right Deltoid


Day 2 Right Axilla: Silver Sulfadiazine present


Day 2 Right Axilla: Silver Sulfadiazine present


Day 1 Upper Back


Day 1 Buttock


Day 2 Sacral and Buttock area

LABORATORY TESTS:

Stable vitals, stable normocytic anemia, mild hyponatremia

DERMATOHISTOPATHOLOGY:

None performed

DIFFERENTIAL DIAGNOSIS:

1.   Systemic Drug Related Intertriginous and Flexural Exanthem (Baboon Syndrome)
2.   Acute Generalized Exanthematous Pustulosis (AGEP)
3.   Fixed Drug Eruption
4.   Drug Rash/Eosinophilia/Systemic Symptoms (DRESS)
5.  


SCROLL DOWN FOR ANSWER AND DISCUSSION.


CORRECT DIAGNOSIS:

Systemic Drug Related Intertriginous and Flexural Exanthem (Baboon Syndrome)

DISCUSSION:

The term ‘baboon syndrome’ was originally introduced in 1984 to describe a mild systemic cutaneous reaction after oral exposure to type IV allergens, such as nickel, mercury or drugs.1 Recently, it has been proposed to replace this term by the acronym SDRIFE (systemic drug-related intertriginous and flexural exanthema).2 100 cases between 1984 and 2004 have been documented with amoxicillin being the most common drug causing SDRIFE, followed by cephalosporins.

The proposed pathophysiology of SDRIFE is most likely a T cell-mediated reaction. The intertriginous and flexural areas are sites that are frequently stimulated mechanically. Mechanically stimulated skin exhibits enhanced expression of intercellular adhesion molecules on the keratinocytes, contributing to the accumulation of drug-activated lymphocytes there.

The criteria that comprise this Systemic Drug Related Intertriginous and Flexural Exanthem (Baboon Syndrome) are:
1. Exposure to a systemically administered drug.
2. Sharply demarcated erythema of the gluteal/perianal area and/or V-shaped erythema of the inguinal/ perigenital area.
3. Involvement of at least one other intertriginous/flexural fold.
4. Symmetry of affected areas;
5. Absence of systemic symptoms and signs.2

Fixed drug eruption (FDE) is clinically distinguishable by its localized, often acral or mucosal, asymmetric, frequently pigmented, round-oval lesions.

Acute generalized exanthematous pustulosis (AGEP) typically presents with a disseminated erythrodermic eruption with primarily non-follicular pustules associated with high fever and sometimes edema of the face.

Drug rash/eosiophilia/systemic symptoms (DRESS) differs from SDRIFE in systemic symptoms, cutaneous signs, organ involvement, eosinophilia and responsible drugs. This difference is important in prognosis, because of the potentially lethal organ involvement such as fulminant hepatitis in DRESS.

SDRIFE is self-limited, and treatment is directed toward discontinuation of offending systemic drug and symptomatic relief. Once offending medication is discontinued, healing occurs in one to two weeks. Medium-to-high potency topical or systemic glucocorticoids may hasten recovery. Avoidance of systemic administration of precipitating allergens is recommended.

TREATMENT:

Change IV antibiotics. Betamethasone to erythematous areas, silver sulfadiazine cream alternating with open cool compresses with Burrows solution to bullous erosive area, pain control, and anti-histamines.

REFERENCES:

Handisurya A et al. SDRIFE (baboon syndrome) induced by penicillin Clin Exp Dermatol 2009;34:355-7.

Hausermann P et al. Baboon syndrome resulting from systemic drugs: is there strife between SDRIFE and allergic contact dermatitis syndrome? Contact Dermatitis 2004;51:297–310.

Additional Comment:


© Copyright 2003-2006 by AOCD Grand Rounds

Top of Page

2010 Academic Year
Latest Case Presentations
Soft Asymptomatic Lesion on the Back
Violaceous Nodule of the Upper Extremity
Patchy Alopecia
Pearly, pink protuberant tumor on the upper extremity
Progressive Hyperpigmented patches
Rash in Nursing Home Patient
An Enlarging Erythematous Plaque with Multiple Draining Sinus Tracts
Persistent and Progressive Hyperpigmented Patches
Painful, Erythematous-Violaceous Plaques Across the Abdomen
Rash in Hospitalized Patient
Painful Eyrthematous Papules
Diffuse Telangiectasias on the bilateral extremities
Chronic Facial Ulcers