Weekly Chest CasesArchive of Old Cases

Case No : 1468 Date 2025-12-08

  • Courtesy of Kum Ju Chae / Jeonbuk National University Hospital
  • Age/Sex 69 / M
  • Chief ComplaintIncidentally found abnormality
  • Figure 1
  • Figure 2
  • Figure 3
  • Figure 4
  • Figure 5
  • Figure 6

Diagnosis With Brief Discussion

Diagnosis
Paraganglioma
Radiologic Findings
Figs 1 and 2. Chest PA and lateral radiographs reveal a large anterior mediastinal mass.
Fig 3. Enhanced chest CT demonstrates a hypervascular anterior mediastinal mass with necrotic changes and enlarged mediastinal lymph nodes.
Figs 4 and 5. MRI shows the mass with T2 high signal intensity, T1 intermediate signal intensity, multifocal necrotic changes, and diffusion restriction. Dynamic scans indicate continuous hyper enhancement.
Fig 6. PET-CT reveals increased FDG uptake in the mass and mediastinal lymph nodes.
Brief Review
Excision of intrathoracic mass revealed paraganglioma of the thorax with regional lymph node metastasis
Paragangliomas of the chest represent 1–2% of all paragangliomas. In the anterior mediastinum, they are usually parasympathetic paragangliomas, often presenting as aorticopulmonary lesions, and are typically asymptomatic, occurring in older patients over 40 years of age. In the posterior mediastinum, they are primarily sympathetic paragangliomas, commonly affecting younger patients with a mean age of 29 years. Approximately half of the cases in the posterior mediastinum are symptomatic.
Image features of paraganglioma shows hypervascular tumor characterized by multiple feeding vessels and a homogeneous capillary blush. It may exhibit hemorrhage or cystic degeneration and demonstrate high T2 signal intensity with early and progressive enhancement on imaging. Additionally, 123I-MIBG scanning is highly specific for their detection. Paragangliomas are not histologically classified as malignant or benign; instead, they are clinically considered malignant if metastasis is present. Approximately 2–13% of paragangliomas are reported to be malignant.
References
1. Hamidi O, Young WF Jr, Iñiguez-Ariza NM, Kittah NE, Gruber L, Bancos C, Tamhane S, Bancos I. Malignant Pheochromocytoma and Paraganglioma: 272 Patients Over 55 Years. J Clin Endocrinol Metab. 2017 Sep 1;102(9):3296-3305. doi: 10.1210/jc.2017-00992. PMID: 28605453; PMCID: PMC5587061.
2. Lee KY, Oh YW, Noh HJ, Lee YJ, Yong HS, Kang EY, Kim KA, Lee NJ. Extraadrenal paragangliomas of the body: imaging features. AJR Am J Roentgenol. 2006 Aug;187(2):492-504. doi: 10.2214/AJR.05.0370. PMID: 16861555.
3. da Silva MCB, Shoji H, Franken M, Shiang C, Garcia RG, Engel FC, Gaiotto FA, Nunes LM, Funari MBG, Szarf G. Paraganglioma: An Uncommon Cause of Mediastinal Mass. Circ Cardiovasc Imaging. 2020 Feb;13(2):e009693. doi: 10.1161/CIRCIMAGING.119.009693. Epub 2020 Jan 31. PMID: 32000513.
Keywords

No. of Applicants : 72

▶ Correct Answer : 1/72,  1.4%
  • - , Japan MASAMICHI IWAI
▶ Correct Answer as Differential Diagnosis : 9/72,  12.5%
  • - Funabashi General Hospital , Japan MANABU AKIMOTO
  • - McGill University Health Center , Canada ALEXANDRE SEMIONOV
  • - Secomedic Hospital , Japan FUMINORI MIYOSHI
  • - Oita University, Faculty of Medicine , Japan FUMITO OKADA
  • - , Japan SHUNJIRO NOGUCHI
  • - Dokkyo Medical University , Japan HIROAKI ARAKAWA
  • - Kyung Hee University Medical Hospital , Korea (South) JEONG TAEK YOON
  • - Matsunami General Hospital , Japan TARO TAKEDA
  • - Nara medical university , Japan HIROHIDE WATANABE
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