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CASE REPORT
Primary erythromelalgia in a child
 
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Online publication date: 2009-04-01
 
 
Reumatologia 2009;47(1):44-47
 
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ABSTRACT
Erythromelalgia is a rare disease of unclear etiology occurring mostly in adults, characterized by increased local skin temperature, burning pain in the feet and less often the hands. This article describes a boy suffering from a primary type of erythromelalgia, and difficulties with achieving a significant improvement with the currently available treatment.
 
REFERENCES (18)
1.
Mitchel SW. On a rare vaso-motor neurosis of the extremities, and on the maladies with which it may be confounded. Am J Med Sci 1878; 76: 17-36.
 
2.
Davis MD, O’Fallon WM, Rogers RS 3rd, Rooke TW. Natural history of erythromelalgia: presentation and outcome in 168 patients. Arch Dermatol 2000; 136: 330-336.
 
3.
Nurowska-Wrzosek B, Tołodziecka L, Gaciong Z. Erytromelalgia: opis dwóch przypadków klinicznych oraz przegląd literatury. Pol Arch Med Wewn 2007; 117: 322-326.
 
4.
Smith LA, Allen EV. Erythermalgia (erythromelalgia) of extremities; a syndrome characterized by redness, heat and pain. Am Heart J 1938; 16: 175-188.
 
5.
Babb RR, Alarcon-Segovia D, Fairbairn JF. Erythermalgia: review of 51 cases. Circulation 1964; 29: 136-141.
 
6.
Strózik K, Lis G, Krzanowska-Dyras M. Case of primary erythromelalgia in a child. Clin Pediatr (Philo) 1992; 31: 378-379.
 
7.
Cohen JS. Erythromelalgia: new theories and new therapies. J Am Acad Dermatol 2000; 43: 841-847. .
 
8.
Finley WH, Lindsey JR Jr, Fine JD, et al. Autosomal dominant erythromelalgia, Am J Med Genet 1992; 42: 310-315. .
 
9.
Yang Y, Wang Y, Li S, et al. Mutations in SCN9A, encoding a sodium channel alpha subunit, in patient with primary erythermalgia. J Med Genet 2004; 41: 171-174.
 
10.
Dib-Hajj SD, Rush AM, Cummins TR, et al. Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons. Brain 2005; 128: 1847-1854.
 
11.
Cohen JS. High-dose oral magnesium treatment of chronic, intractable erytromelalgia. Ann Pharmacother 2002; 36: 255-260.
 
12.
Davis MD, Sandroni P. Lidocaine patch for pain of erythromelalgia: follow up of 34 patients. Arch Dermatol 2005; 141: 1320-1321. .
 
13.
Nathan A, Rose JB, Guite JW, et al. Primary erythromelalgia in a child responding to intravenous lidocaine and oral mexiletine treatment. Pediatrics 2005; 115: 504-507.
 
14.
Chan MK, Tucker AT, Madden S, Golding CE, Atherton DJ, Dillon MJ; Erythromelalgia: an endothelial disorder responsive to sodium nitroprusside. Arch Dis Child 2002; 87: 229-230. .
 
15.
Harrison CM, Goddard JM, Rittey CD. The use of regional anaesthetic blockade in a child with recurrent erythromelalgia. Arch Dis Child 2003; 88: 65-66.
 
16.
Stricker LJ, Green CR. Resolution of refractory symptoms of secondary erythermalgia with intermittent epidural bupivacaine. Reg Anesth Pain Med 2001; 26: 488-490.
 
17.
Seishima M, Kanoh H, Izumi T, et al. A refractory case of secondary erythermalgia successfully treated with lumbar sympathetic ganglion bloc. Br J Dermatol 2000; 143: 868-872. .
 
18.
Sheets PL, Jackson JO 2nd,Waxman SG, et al. A Navi 1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity. J Physiol 2007; 581: 1019-1031.
 
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