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

Author:

Ben Nacef Ibtissem1ORCID,Mekni Sabrine1,Mhedhebi Chedi1,Riahi Ines2,Rojbi Imen1,Nadia Mchirgui1,Khiari Karima1

Affiliation:

1. Department of Endocrinology, Charles Nicolle Hospital, Tunis, Tunisia

2. Department of Otorhinolaryngology-Head and Neck Surgery, Charles Nicolle Hospital, Tunis, Tunisia

Abstract

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.

Publisher

Hindawi Limited

Subject

Endocrinology, Diabetes and Metabolism

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