From normal to abnormal MR findings within three weeks in a solitary pelvic Langerhans histiocytosis

Po-Cheng Hung1, Huei-Shyong Wang, Tang-Her Jaing

  • 1Division of Pediatric Neurology, Chang Gung Children's Hospital, College of Medicine Chang Gung University, Taoyuan, Taiwan. hongfh@ms14.hinet.net

Skeletal Radiology
|July 5, 2003
PubMed

Insights

Pelvic Langerhans histiocytosis, also known as eosinophilic granuloma, can present as a new abnormality on MRI scans. This rare condition may mimic infection on imaging, highlighting the need for careful diagnosis.

Area of Science:

  • Oncology
  • Radiology
  • Pediatric Pathology

Background:

  • Langerhans cell histiocytosis (LCH) is a rare clonal proliferative disorder of Langerhans cells.
  • Pelvic involvement in LCH, particularly in adults, is uncommon.
  • Eosinophilic granuloma is a term often used for the localized, unifocal form of LCH.

Observation:

  • A case of histologically confirmed pelvic Langerhans histiocytosis is presented.
  • Initial magnetic resonance (MR) imaging was normal.
  • A follow-up MR examination three weeks later revealed new abnormalities.

Findings:

  • The MR imaging findings in the follow-up examination mimicked an infectious process.
  • The progression of findings on serial MR imaging is a key diagnostic clue.
  • Histological confirmation established the diagnosis of Langerhans histiocytosis.

Implications:

  • This case underscores the importance of considering Langerhans histiocytosis in the differential diagnosis of pelvic lesions, even with initially normal imaging.
  • Serial imaging can be crucial for detecting subtle changes and guiding diagnosis in rare conditions.
  • Radiologists and clinicians should be aware of the potential for Langerhans histiocytosis to mimic infection on pelvic MRI.

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