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A Case of Langerhans Cell Histiocytosis Involving the
Thyroid Gland: Ultrasonographic Finding |
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Yook Kim, MD1 Seung Young Lee, MD1, Sang Hoon Cha, MD1,
Gyeong Sik Lee, MD2, Bum Sang Cho, MD2, Min Ho Gang, MD2 |
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1Department of Radiology, College of Medicine and Medical Research Institute, Chungbuk
National University
2Department of Radiology, Chungbuk National University Hospital |
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Langerhans cell histiocytosis is a rare, proliferative monoclonal histiocytic disease of
unknown cause. Primary involvement of the thyroid gland by LCH is very rare, and
most cases show evidence of LCH involving other organs. Herein, we report on a
case of thyroid LCH in a patient diagnosed as pituitary gland LCH. When a patient
with a history of LCH presents with enlargement of the thyroid gland or a neck mass,
and ultrasonography shows a well-defined low echoic mass, LCH should be included
in differential diagnosis. Fine needle aspiration can be useful for initial diagnosis; however,
for differentiation with thyroiditis or thyroid cancer, core biopsy, positive S-100
protein, and CD1a immunohistochemical staining are needed. |
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Keyword : Langerhans cell histiocytosis; Thyroid gland; Ultrasonographic finding |
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pdf파일 : 67-70김육20.pdf
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