Imaging findings of primary immunoglobulin G4-related cervical lymphadenopathy

Masaya Kawaguchi1, Hiroki Kato2, Yusuke Kito3

  • 1Department of Radiology, Gifu University School of Medicine, 1-1 Yanagido, Gifu, 501-1194, Japan.

Neuroradiology
|September 18, 2017
PubMed

Insights

Imaging findings in immunoglobulin G4 (IgG4)-related cervical lymphadenopathy were assessed. Most enlarged nodes were unilateral, located in the submandibular region, and lacked central necrosis or significant perinodal infiltration.

Area of Science:

  • Radiology
  • Oncology
  • Immunology

Background:

  • Immunoglobulin G4 (IgG4)-related disease is a systemic fibroinflammatory condition.
  • Cervical lymphadenopathy can be a manifestation of IgG4-related disease.
  • Accurate imaging assessment is crucial for diagnosis and management.

Purpose of the Study:

  • To evaluate the imaging characteristics of primary immunoglobulin G4 (IgG4)-related cervical lymphadenopathy.
  • To identify key imaging features that aid in the diagnosis of this condition.

Main Methods:

  • Retrospective review of imaging data from five patients with confirmed IgG4-related cervical lymphadenopathy.
  • Analysis included contrast-enhanced computed tomography (CT) and 18F-fluorodeoxyglucose (FDG)-positron emission tomography (PET)/CT scans.
  • Assessment of lymph node characteristics such as size, location, necrosis, infiltration, and metabolic activity (SUVmax).

Main Results:

  • Thirteen enlarged cervical lymph nodes were identified, predominantly unilateral.
  • The majority of enlarged nodes (62%) were located in the submandibular region (level IB).
  • Central necrosis and significant perinodal infiltration were uncommon; penetrating vessels were observed in 54% of nodes.

Conclusions:

  • Primary IgG4-related cervical lymphadenopathy typically presents as unilateral, submandibular lymphadenopathy.
  • Absence of central necrosis and minimal perinodal infiltration are characteristic imaging findings.
  • Imaging features, including SUVmax, can help differentiate IgG4-related lymphadenopathy from other causes.
Abstract