[Langerhans cell histiocytosis presenting as isolated adenitis in an infant: case report]

María Soriano-Ramos1, Enrique Salcedo Lobato2, María Baro Fernández2

  • 1Servicio de Pediatría, Fundación para la Investigación Biomédica Hospital 12 de Octubre, Universidad Complutense, Hospital Universitario 12 de Octubre, Madrid, España. sorianoramosmaria@gmail.com.

Insights

Langerhans cell histiocytosis, a rare infant condition, can present as an isolated neck mass. Early diagnosis via fine needle aspiration is crucial for infants with unresponsive neck swelling.

Area of Science:

  • Pediatric Oncology
  • Dermatology
  • Pathology

Background:

  • Langerhans cell histiocytosis (LCH) is a rare clonal proliferative disorder of Langerhans cells.
  • Infantile LCH typically presents with multisystem involvement, making isolated cervical adenitis exceptional.

Observation:

  • A 3-month-old infant presented with a right mandibular angle neck mass unresponsive to antibiotics.
  • The mass was initially suspected to be infectious or inflammatory due to its presentation.

Findings:

  • Fine needle aspiration (FNA) confirmed Langerhans cell histiocytosis.
  • Further tests revealed no evidence of systemic LCH involvement, indicating localized disease.

Implications:

  • Langerhans cell histiocytosis should be considered in the differential diagnosis of subacute neck masses in infants.
  • Prompt FNA is recommended for infants with neck masses exhibiting poor treatment response to establish a definitive diagnosis and guide management.

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