Journal of cutaneous medicine and surgery · 2009
Acral, pure cutaneous, self-healing, late-onset, cellulitis-like Langerhans cell histiocytosis.
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Sharma Prafulla Kumar, Sabhnani Sunil, Bhardwaj Minakshi, Kar Hemanta Kumar
Аннотация
BACKGROUND: An unusual and not yet reported clinical presentation of pure cutaneous Langerhans cell histiocytosis (LCH) that was a diagnostic dilemma.
OBJECTIVE: To bring to light the newer presentation of this disease.
METHOD: The case was managed on clinical grounds initially as cellulitis. However, after the investigations and confirmation of the diagnosis, she was managed symptomatically.
RESULTS: Pure cutaneous LCH may manifest in early adulthood with features of cellulitis, erythematous edematous vesicular plaques, and nodules distributed in the flexural acral areas.
CONCLUSION: Pure cutaneous LCH may have an acute late onset with unusual morphology as cellulitis, inverse acral distribution, and self-healing.
OBJECTIVE: To bring to light the newer presentation of this disease.
METHOD: The case was managed on clinical grounds initially as cellulitis. However, after the investigations and confirmation of the diagnosis, she was managed symptomatically.
RESULTS: Pure cutaneous LCH may manifest in early adulthood with features of cellulitis, erythematous edematous vesicular plaques, and nodules distributed in the flexural acral areas.
CONCLUSION: Pure cutaneous LCH may have an acute late onset with unusual morphology as cellulitis, inverse acral distribution, and self-healing.