Cutaneous Langerhans cell histiocytosis presenting with hypopigmented lesions: Report of two cases and review of literature |
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Authors: | Shoko Mori BS Tony Adar MD Viktoryia Kazlouskaya MD Jaime B. Alexander MD Edward Heilman MD Sharon A. Glick MD |
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Affiliation: | Department of Dermatology, State University of New York Downstate Medical Center, Brooklyn, NY, USA |
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Abstract: | Langerhans cell histiocytosis is a rare group of disorders that results from the abnormal proliferation and accumulation of dendritic‐derived cells in various organs of the body, such as the skin and bones. Hypopigmented macules are a rare cutaneous presentation of Langerhans cell histiocytosis that may pose a diagnostic dilemma when no other findings of Langerhans cell histiocytosis are present at the time of examination. We present 2 cases of the hypopigmented variant of Langerhans cell histiocytosis, including a case with histopathologic features of regression, and a review of the literature. These cases highlight the importance of including Langerhans cell histiocytosis in the differential diagnosis of an infant with hypopigmented macules and papules. |
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Keywords: | histiocytic disorders skin signs of systemic disease |
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