Volume 51, Issue 6 pp. 833-835
Brief Report

Thymic Langerhans cell histiocytosis mimicking lymphoma

Begül Yağcı MD

Corresponding Author

Begül Yağcı MD

Department of Pediatric Oncology, Hacettepe University Institute of Oncology, Ankara, Turkey

Fellow of Pediatric Oncology, Department of Pediatric Oncology, Hacettepe University Institute of Oncology, 06100 Ankara, Turkey.===Search for more papers by this author
Ali Varan MD

Ali Varan MD

Department of Pediatric Oncology, Hacettepe University Institute of Oncology, Ankara, Turkey

Professor of Pediatrics and Pediatric Oncologist.

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Ayşegül Üner MD, PhD

Ayşegül Üner MD, PhD

Department of Pathology, Hacettepe University Faculty of Medicine, Ankara, Turkey

Professor of Pathology.

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Canan Akyüz MD

Canan Akyüz MD

Department of Pediatric Oncology, Hacettepe University Institute of Oncology, Ankara, Turkey

Professor of Pediatrics and Pediatric Oncologist.

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Münevver Büyükpamukçu MD

Münevver Büyükpamukçu MD

Department of Pediatric Oncology, Hacettepe University Institute of Oncology, Ankara, Turkey

Professor of Pediatrics and Pediatric Oncologist.

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First published: 09 October 2008
Citations: 10

Abstract

Langerhans cell histiocytosis (LCH) is a rare disorder characterized by clonal expansion of antigen presenting Langerhans cells. Different clinical features can be seen according to the involved organs and sytems. Multisystem disease with organ dysfunction is more common in infants, whereas single system disease is usually observed in older children. The disease can affect any system or organ throughout the body. Thymus is a rarely involvement site reported in LCH and usually is accompanied by skin, bone or lung disease. Here we report a 12-year-old male with thymic involvement by LCH clinically mimicking lymphoma. Pediatr Blood Cancer 2008;51:833–835. © 2008 Wiley-Liss, Inc.

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