Case Reports in Endocrinology (Jan 2020)

Langerhans Cell Histiocytosis of the Thyroid Leading to the Diagnosis of a Disseminated Form

  • Ibtissem Ben Nacef,
  • Sabrine Mekni,
  • Chedi Mhedhebi,
  • Ines Riahi,
  • Imen Rojbi,
  • Mchirgui Nadia,
  • Karima Khiari

DOI
https://doi.org/10.1155/2020/6284764
Journal volume & issue
Vol. 2020

Abstract

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Langerhans cell histiocytosis (LCH) is a rare sporadic proliferative disorder of Langerhans cells. LCH rarely involves the thyroid gland. We report herein a case of a disseminated chronic form of LCH with a diagnosis established by histological examination of the thyroid gland. It is about a 37-year-old female who underwent total thyroidectomy for a thyroid nodule of the right lobe. Histological study showed a granulomatous thyroiditis, and the immunohistochemistry study revealed a strong positivity of histiocytes for the CD1 antigen and for the S100 protein. The incidence of LCH involving the thyroid gland, either as an isolated lesion or as a part of multisystemic disease, is extremely rare.