Langerhans cell histiocytosis followed by hodgkin lymphoma: a case report

Akbar Safaei1, Mandana Bagheri1, Jahanbanoo Shahryari1

  • 1Department of Pathology, Molecular Pathology and Cytogenetic Ward, Shiraz University of Medical Sciences, Iran;

Insights

Langerhans cell histiocytosis (LCH), typically benign, rarely progresses to malignancy. This case report details a rare instance of LCH followed by Hodgkin lymphoma, highlighting unusual disease progression.

Area of Science:

  • Oncology
  • Hematology
  • Pathology

Background:

  • Langerhans cell histiocytosis (LCH) is a rare clonal proliferative disease of bone marrow-derived Langerhans cells.
  • Characterized by CD1a and S100 expression and Birbeck granules, LCH typically presents as a benign neoplasm, though rare malignant transformations occur.

Observation:

  • This study presents a unique case of Langerhans cell histiocytosis (LCH) followed by Hodgkin lymphoma (HL).

Findings:

  • The co-occurrence of LCH and malignant lymphoma is exceptionally rare.
  • While malignant lymphoma preceding LCH has been documented, LCH developing after lymphoma is seldom reported.

Implications:

  • This case contributes to understanding the rare but possible progression of LCH to secondary malignancies.
  • Further research is warranted to elucidate the mechanisms underlying LCH transformation and its association with other hematological neoplasms.

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