Abstract

BackgroundThis study aimed to identify the characteristic radiological signs for the diagnosis of Langerhans cell histiocytosis (LCH) of the bone.MethodsWe retrospectively studied 82 cases of LCH with bone lesions confirmed by pathology. Clinical and radiological features of the patients were analyzed.ResultsA total of 64 and 18 patients had single and multiple bone lesions, respectively. With regard to LCH with single bone lesions, 37.5% (24/64) of lesions were located in the skull and presented as bone destruction with or without soft tissue mass. The correct diagnosis rate of these lesions was 60.0% (9/15) in children and adolescents, but was only 22.2% (2/9) in adults.A total of 26.5% (17/64) of the solitary lesions were found in the spine. Of these, 88.2% (15/17) were located in the vertebral body and appeared to have different degrees of collapse, and 66.7% (10/15) of these lesions were correctly diagnosed.Of the unifocal lesions, 21.8% (14/64) were located in other flat and irregular bones and manifested as osteolysis. Only 21.4% (3/14) of these cases were correctly diagnosed.In total, 14.1% (9/64) of the isolated bone LCH lesions were located in the long bones. Of these, 77.8% (7/9) were located in the diaphysis and presented as central bone destruction with or without fusiform periosteal reaction and extensive peripheral edema, of which 42.9% (3/7) were correctly diagnosed before surgery or biopsy.With regard to LCH with multiple bony destructive lesions, 71.4% (10/14) of cases in children and adolescents were correctly diagnosed; however, all four cases among adults were misdiagnosed.ConclusionIn all age groups, isolated diaphyseal destruction of the long bone with fusiform periosteal reaction and extensive peripheral edema, vertebra plana of the spine, and bevelled edge of skull defects accompanied by soft tissue masses strongly suggest LCH diagnosis. Moreover, the multiple bone osteolytic destruction in children and adolescents strongly suggests LCH diagnosis. Familiarity with these typical radiological signs of LCH is necessary to decrease misdiagnoses.

Highlights

  • This study aimed to identify the characteristic radiological signs for the diagnosis of Langerhans cell histiocytosis (LCH) of the bone

  • LCH is categorized as a single-system LCH (SS-LCH) with multifocal or unifocal involvement, or as multisystem LCH (MS-LCH) with multiple organ involvement with or without risk organ involvement

  • Radiographic findings and diagnosis Regarding LCH with single bone lesions, 37.5% (24/64) of lesions were located in the skull/cranial-facial bone

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Summary

Introduction

This study aimed to identify the characteristic radiological signs for the diagnosis of Langerhans cell histiocytosis (LCH) of the bone. LCH, the most common histiocytic disorder, is characterized by the accumulation of CD1A+/CD207+ mononuclear phagocytes within granulomatous lesions that can affect most organ systems. Organs at risk include the hematopoietic system (bone marrow), spleen, and liver [3]. LCH may affect any organs, but those more frequently affected are the bones (80% of cases), skin (33%), pituitary gland (25%), liver, spleen, hematopoietic system, lungs (15% each), lymph nodes (5–10%), or the central nervous system (CNS) (2–4%, excluding the pituitary) [4]. Radiological measures, including computed tomography (CT) and magnetic resonance imaging (MRI), are recommended to evaluate LCH and assist in diagnosis [6]

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