Multicentrisk retikulohistiocytose er en sjælden form for paraneoplasi

Anna Maria Anderson, Tanja Todberg, Kristian Kofoed, Trine Zeeberg Iversen, Martin Andersen, Sofie Vetli Hjorth, Daniel El Fassi

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Abstract

A 59-year-old woman developed a rash and severe arthralgia, which primarily affected her fingers. She displayed digital arthritis and nodules on the hands, chest, face, and oral cavity. Blood samples were normal. Skin biopsies revealed histiocytic proliferation. The surface marker profile and clinical findings were consistent with multicentric reticulohistiocytosis, which may occur as a paraneoplastic phenomenon. On workup, she was diagnosed with an otherwise asymptomatic stage IVC fallopian tube cancer. She experienced little effect of prednisolone, but her condition improved on antineoplastic treatment.

Bidragets oversatte titelMulticentric reticulohistiocytosis is a rare form of paraneoplasia
OriginalsprogDansk
ArtikelnummerV08170611
TidsskriftUgeskrift for Laeger
Vol/bind180
Udgave nummer11
Antal sider2
ISSN0041-5782
StatusUdgivet - 2018

Emneord

  • Adenocarcinoma/complications
  • Antineoplastic Agents/therapeutic use
  • Fallopian Tube Neoplasms/complications
  • Female
  • Hand/pathology
  • Histiocytosis, Non-Langerhans-Cell/diagnosis
  • Humans
  • Middle Aged
  • Rare Diseases

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