Sea-blue histiocytosis

Ann Pathol. 2024 Mar;44(2):150-151. doi: 10.1016/j.annpat.2023.10.001. Epub 2023 Oct 19.

Abstract

A 78-year-old woman with hypertrophic cardiomyopathy underwent a septal myomectomy and valve replacement. In the immediate postoperative period she developed shock of mixed etiology and died. At autopsy, hepatomegaly and splenomegaly were identified, with PAS and Giemsa positive intracellular ceroid granular deposits. Sea-blue histiocytosis is an extremely rare, chronic and benign deposit disease. It is characterized by hepatosplenomegaly, thrombocytopenia and lymphadenopathy. The presence of ceroid substance in granules in PAS and Giemsa stains should establish the diagnosis of suspicion.

Keywords: Bleu marine; Cardiomyopathie hypertrophique; Ceroid; Céroïde; Défaillance multiorganique; Giemsa; Granules; Histiocytose; Histiocytosis; Hypertrophic cardiomyopathy; Multiorgan failure; PAS; Sea blue.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Ceroid
  • Female
  • Hepatomegaly / etiology
  • Humans
  • Sea-Blue Histiocyte Syndrome* / complications
  • Sea-Blue Histiocyte Syndrome* / diagnosis
  • Splenomegaly / complications

Substances

  • Ceroid