Primary localized amyloidosis manifested as supraclavicular and mediastinal lymphadenopathy.

H. S. Yong, O. H. Woo, J. W. Lee, S. I. Suh, Y. W. Oh, E. Y. Kang

    Research output: Contribution to journalArticlepeer-review

    10 Citations (Scopus)


    Thoracic involvement of amyloidosis is relatively rare, but mediastinal lymphadenopathy in the absence of pulmonary parenchymal involvement is extremely rare. The case presented here is of a previously healthy elderly woman who developed a palpable mass in the right supraclavicular area. The chest CT scan showed extensive, contiguous and homogeneous low attenuated lymphadenopathy with stippled calcification in the right supraclavicular area and mediastinum. Amyloidosis was confirmed histopathologically on a biopsy specimen from a right supraclavicular lymph node. Because there were no other sites found to be affected by amyloidosis and there was no underlying chronic disease, we made a final diagnosis of primary localized amyloidosis involving only the supraclavicular and mediastinal lymph nodes.

    Original languageEnglish
    Pages (from-to)e131-133
    JournalThe British journal of radiology
    Issue number955
    Publication statusPublished - 2007 Jul

    ASJC Scopus subject areas

    • Radiology Nuclear Medicine and imaging


    Dive into the research topics of 'Primary localized amyloidosis manifested as supraclavicular and mediastinal lymphadenopathy.'. Together they form a unique fingerprint.

    Cite this