Isolated Langerhans Cell Histiocytosis of the Thyroid: A very rare case report

Year 2024, , 163 - 166, 29.10.2024

Ali Erol , Hilmi Gözden , Sinan Koç , Hatice Kuzular

https://doi.org/10.46310/tjim.1528707

Abstract

Langerhans cell histiocytosis (LCH) is a group of diseases that cause damage by local or widespread accumulation of atypical histiocytes in various tissues such as skin, bone, lung, liver, lymph nodes, mucocutaneous tissues, and endocrine organs. LCH was detected as a result of a total thyroidectomy biopsy performed on a 43-year-old female patient with a solitary euthyroid nodule following weight loss and an increase in the size of the thyroid nodule during outpatient clinic checks. Patient's whole body positron emission tomography. The case of LCH with isolated thyroid involvement is very rare, and a limited number of cases have been presented on this subject. In addition, it will contribute to the literature since there are fewer than ten LCH cases with thyroid involvement.

Keywords

Langerhans cell histiocytosis, fine needle aspiration biopsy, thyroid

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