Case Report: A rare adult multisystem Langerhans cell histiocytosis involving the skin, thyroid, jaw-periodontal region, and bone: diagnostic challenges and complementary PET/CT–SPECT/CT findings
Longchuan Zhuang, Kexu Chen, Xiaokun Qi, Jie Li, Song Qin, Hua Yu, Minggang Yuan

TL;DR
This case report describes a rare multisystem Langerhans cell histiocytosis in a 32-year-old man, highlighting diagnostic challenges and the complementary use of PET/CT and SPECT/CT imaging.
Contribution
The case emphasizes the role of serial PET/CT and bone scintigraphy in managing adult multisystem LCH.
Findings
PET/CT showed extensive cutaneous and extracutaneous involvement, including bone, thyroid, and lung.
After chemotherapy, PET/CT showed metabolic remission, but bone scintigraphy revealed ongoing skeletal remodeling.
The case underscores the importance of early biopsy and multimodal imaging for accurate diagnosis and monitoring.
Abstract
Langerhans cell histiocytosis (LCH) is a rare clonal myeloid neoplasm with prominent inflammatory features and heterogeneous manifestations in adults, often leading to diagnostic delay. We report a 32-year-old man who presented with a two-year history of recurrent ulcerative intertriginous skin lesions refractory to empirical treatment for presumed inflammatory or infectious dermatoses. Biopsy from the ulcer edge showed atypical histiocytoid cells with characteristic nuclear grooves and numerous eosinophils; immunohistochemistry was positive for CD1a, S-100, and Langerin with a Ki-67 index of ~40%, confirming cutaneous LCH. Baseline 18F-FDG PET/CT (August 2022) demonstrated multisystem disease with extensive cutaneous involvement and imaging-suggestive involvement of multiple extracutaneous sites, including multifocal osseous lesions, the thyroid, gastrointestinal tract, lymph nodes,…
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Taxonomy
TopicsHistiocytic Disorders and Treatments · Oral and Craniofacial Lesions · Viral-associated cancers and disorders
