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Congenital Langerhans cell histiocytosis with skin and lung involvement: Spontaneous regression
Authors:Varun Aggarwal  Anju Seth  Manjula Jain  Sriram Krishnamurthy  Varkha Chandra  Satinder Aneja
Affiliation:1.Department of Pediatrics,Lady Hardinge Medical College and Kalawati Saran Children’s Hospital,New Delhi,India;2.Department of Pathology,Lady Hardinge Medical College and Kalawati Saran Children’s Hospital,New Delhi,India
Abstract:Congenital self-healing Langerhans cell histiocytosis (CSHLCH) is a rare type of Langerhans Cell Histiocytosis, presenting at birth or during the neonatal period with eruption of multiple, discrete red-brown papules or nodules that undergo spontaneous regression. Systemic signs are generally absent. We describe a 4-month-old infant presenting with reddish brown nodular cutaneous lesions since birth with a past history suggestive of pulmonary involvement. Skin biopsy showed a dermal infiltrate of pleomorphic histiocytes; which were CD1a and S-100 positive, consistent with the diagnosis of CSHLCH. Both pulmonary and cutaneous lesions showed spontaneous resolution.
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