Case Report: PDF OnlyLangerhans Cell Histiocytosis in a NewbornYang, Tzu-Yinga; Chen, Shu-Jena, *; Yang, Ling-Yua, b; Tang, Ren-Bina, b Author Information aDepartment of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan, R.O.C. bInstitute of Clinical Medicine, National Yang-Ming University School of Medicine, Taipei, Taiwan, R.O.C. *Correspondence to: Dr Shu-Jen Chen, Department of Pediatrics, Taipei Veterans General Hospital, 201, Section 2, Shih-Pai Road, Taipei 112, Taiwan, R.O.C. E-mail: [email protected] Received: December 29, 2008; • Accepted: September 21, 2009. Journal of the Chinese Medical Association 72(11):p 611-614, November 2009. | DOI: 10.1016/S1726-4901(09)70439-3 Metrics Abstract A full-term female baby was admitted to our hospital at the postnatal age of 37 days with generalized vesiculopapular, crateriform skin lesions. Physical examination revealed a well-nourished baby without fever, hepatosplenomegaly or lymphadenopathy. Laboratory examination was normal except for thrombocytosis (platelet count, 970 × 103/μL). All studies for herpes simplex virus, including culture, polymerase chain reaction and IgM, were negative except for an antigen test from the vesicles for herpes simplex virus type 1, which was positive. Chest X-ray showed increased reticulogranular infiltration over bilateral lung fields and some osteolytic lesions at the left parietal bone. Skin biopsy revealed infiltration of Langerhans cells and eosinophils, plus positive CD1a and S-100 stains. The diagnosis was reconfirmed by a second hospital and chemotherapy was given. In this case report, the differential diagnoses of neonatal vesiculopapular skin lesions, and the classification and outcome of neonatal Langerhans cell histiocytosis are presented. © 2009 by Lippincott Williams & Wilkins, Inc.