Mainly adrenal gland involving NK/T-cell nasal type lymphoma diagnosed with delay due to mimicking adrenal hemorrhage

  • Seon Mee Kang
  • , Woong Ji Kim
  • , Kyung Ae Lee
  • , Hong Sun Baek
  • , Tae Sun Park
  • , Heung Yong Jin*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

A 29-yr-old man, presented with abdominal pain and fever, had an initial computed tomography (CT) scan revealing low attenuation of both adrenal glands. The initial concern was for tuberculous adrenalitis or autoimmune adrenalitis combined with adrenal hemorrhage. The patient started empirical anti-tuberculous medication, but there was no improvement. Enlargement of cervical lymph nodes were developed after that and excisional biopsy of cervical lymph nodes was performed. Pathological finding of excised lymph nodes was compatible to NK/T-cell lymphoma. The patient died due to the progression of the disease even after undergoing therapeutic trials including chemotherapy. Lymphoma mainly involving adrenal gland in the early stage of the disease is rare and the vast majority of cases that have been reported were of B-cell origin. From this case it is suggested that extra-nodal NK/T-cell lymphoma should be considered as a cause of bilateral adrenal masses although it is rare.

Original languageEnglish
Pages (from-to)1386-1390
Number of pages5
JournalJournal of Korean Medical Science
Volume26
Issue number10
DOIs
StatePublished - 2011.10

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Bilateral adrenal masses
  • Extra-nodal lymphoma
  • Natural killer (NK)/T-cell nasal type lymphoma

Quacquarelli Symonds(QS) Subject Topics

  • Medicine

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