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A case of recurrent pseudolymphomatous folliculitis: A mimic of cutaneous lymphoma

  • Eun Ji Kwon
  • , Arni K. Kristjansson
  • , Howard J. Meyerson
  • , Gregory M. Fedele
  • , Rebecca C. Tung
  • , Klaus Sellheyer
  • , Ralph J. Tuthill
  • , Kord S. Honda
  • , Anita C. Gilliam
  • , Jennifer M. McNiff

Rannsóknarafurð: Framlag til fræðitímaritsGreinritrýni

Útdráttur

Pseudolymphomatous folliculitis is a rare entity. We present a 62-year-old man with a recurrent solitary nodule on his nose requiring multiple excisions. Microscopic examination of the excisions showed a dense lymphocytic infiltrate containing numerous histiocytes and S100+, CD1a+ dendritic cells that surrounded and infiltrated hypertrophic hair follicles. Diffuse sheets of CD3+ T cells and nodular clusters of CD20+ B cells were also seen. There was normal reactive pattern of follicular centers. Light chain restriction was not detected. T-cell receptor and immunoglobulin heavy chain gene rearrangements by polymerase chain reaction revealed negative findings. A diagnosis of pseudolymphomatous folliculitis was made based on the hypertrophic hair follicles, periadnexal S100+ and CD1a+ dendritic cells, and negative clonal gene rearrangement study findings. This case of recurrent pseudolymphomatous folliculitis is instructive because of the resemblance to cutaneous lymphomas and cutaneous lymphoid hyperplasias, and the need for correct diagnosis to avoid overtreatment of this indolent condition.

Upprunalegt tungumálEnska
Síður (frá-til)994-1000
Síðufjöldi7
FræðitímaritJournal of the American Academy of Dermatology
Bindi60
Númer tölublaðs6
DOI
ÚtgáfustaðaÚtgefið - jún. 2009

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