A rare case of angiomyomatous hamartoma of periaortic lymph node and synchronous angiomyolipoma of the kidney: a diagnostic pitfall for lymph node involvement by angiomyolipoma

Zsolt Jobbagy, Claudio Guerrieri, Domenico Savatta, Sairam Chattu, Billie Fyfe-Kirschner

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Angiomyomatous hamartoma is a rare benign proliferative lesion of lymph nodes, showing replacement of the lymph node parenchyma by irregular thick-walled blood vessels, smooth muscle, fibrotic stroma and variable amount of adipose tissue. These histologic features greatly overlap with those described in angiomyolipoma, a member of the perivascular epithelioid cell tumor (PEComa) family. We present a unique case of angiomyomatous hamartoma of a periaortic lymph node, which mimicked lymph node involvement in a patient with renal angiomyolipoma on hematoxylin and eosin (H&E) stained slides alone.

Original languageEnglish
Article number200361
JournalHuman Pathology: Case Reports
Volume19
DOIs
StatePublished - Mar 2020
Externally publishedYes

Keywords

  • Angiomyolipoma in lymph node
  • Angiomyomatous hamartoma
  • Cathepsin K
  • Melanocytic immunomarkers
  • Periaortic lymph node
  • Renal angiomyolipoma

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