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Indian Pediatr 2011;48: 584

Erythema Nodosum as the Presenting Feature of Rheumatic Heart Disease


Syed Ahmed Zaki and Preeti Shanbag,

Department of Pediatrics, Lokmanya Tilak Municipal General Hospital and Medical College, Sion, Mumbai, India.
Email: [email protected]

 


A nine-year-old boy presented with multiple painful nodular lesions on the extensor aspect of bilateral elbow and knee joints since 15 days (Fig. 1). There was no sore throat, pyoderma, arthralgia, abdominal pain, drug intake or Koch’s contact. On enquiry, fever and exertional dyspnea were present since 5 days. Grade III/VI pansystolic murmur was present in the mitral area. Chest x-ray and ultrasonography of abdomen were normal. Mantoux test was negative. Antistreptolysin titre, erythrocyte sedimentation rate and C-reactive protein were elevated. Echocardiography showed moderate mitral regurgitation. Histopathology of the nodular lesions was consistent with erythema nodosum (EN). With a diagnosis of rheumatic heart disease and active carditis, benzathine penicillin prophylaxis and aspirin were started. On follow up after 3 weeks, the nodules had disappeared.

Fig. 1 Nodular lesions on the extensor aspect of bilateral elbow and knee joints.

EN is a symmetric inflammatory process involving the subcutaneous fat that causes tender, erythematous nodules. Sites involved are pretibial (most common), extensor surfaces of forearm, legs, thighs, and trunk. The lesions do not ulcerate and resolve without atrophy or scarring in one to two months. EN is a cutaneous immune-mediated (type IV delayed hypersensitivity) reaction to a variety of antigens. Commonly associated conditions include streptococcal infection, tuberculosis, sarcoidosis, sulphonamides, amoxicillin, inflammatory bowel disease, lymphoma, amoebiasis, giardiasis and viral infections (hepatitis B & C, herpes simplex, HIV and EBV). Common differential diagnoses include infectious panniculitis, lupus panniculitis, cold panniculitis, leukemic infiltrates, necrobiosis lipoidica, lipodystrophies and scleroderma. Management includes treatment of underlying disorders and supportive care i.e. bed rest, avoiding contact irritation of affected areas, non-steroidal anti-inflammatory drugs for pain and systemic steroids.
 

 

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