TNF receptor-associated periodic syndrome
TRAPS was initially described in individuals of Irish or Scottish descent, although it has now been described in a broad range of ethnic groups. There is a slight male preponderance. The onset of TRAPS can occur from 3 weeks to 28 years of age (median age 3 years). In most patients, disease onset occurs before 10 years of age.
Individuals with TRAPS have episodes of fever, abdominal pain (up to 70%), periorbital edema, arthralgias or arthritis, and migratory erythema. Fevers ranging from 38°C-41°C (100.4°F-105.8°F) may precede skin and muscle symptoms. Skin lesions (in up to 85% of affected patients) include erythematous patches and/or plaques with an annular or serpiginous morphology that migrate centripetally, often in association with muscle tenderness. Ecchymotic and purpuric lesions may occur. Other findings may include lymphadenopathy, pericarditis, pleurisy, testicular pain, and inguinal hernias. Lymphadenopathy and periorbital edema are more common in pediatric patients whereas pericarditis is observed more frequently in adult-onset TRAPS.
Attacks occur at random and can last from days to a few weeks, with an average duration of 3 weeks.
TRAPS may improve during pregnancy.
Reactive amyloidosis is a long-term consequence of TRAPS due to deposition of serum amyloid A fibrils in organs including the kidneys, liver, and spleen.
Pediatric Patient Considerations:
In nearly 90% of patients, the first skin eruption is noted during the first 2 years of life.
E85.0 – Non-neuropathic heredofamilial amyloidosis
403833009 – TNF receptor-associated periodic fever syndrome (TRAPS)
- Other periodic fever syndromes, including familial Mediterranean fever (FMF) and hyperimmunoglobulinemia D syndrome with periodic fever (HIDS). FMF and HIDS are inherited in autosomal recessive fashion. TRAPS attacks are longer (4-21 days) than those of other familial fever syndromes. FMF is most common in individuals of Jewish, Armenian, Arab, Italian, and Turkish ancestry while TRAPS is found in many ethnic groups. HIDS often presents with lymphadenopathy that is not typically present in TRAPS or FMF; 95% of patients with HIDS have elevated serum IgD.
- Muckle-Wells syndrome (MWS) is an autosomal dominant familial fever syndrome associated with urticaria and deafness; see cryopyrin-associated periodic syndromes (CAPS).
- Lyme disease may be suggested by large annular migratory urticarial papules and/or plaques that appear during temperature spikes and disappear when patient is afebrile.
- Erythema marginatum – Evanescent wispy, serpiginous, annular, and figurate erythematous papules and plaques; occurs in association with rheumatic fever.
Juvenile rheumatoid arthritis