Skip to main navigation Skip to search Skip to main content

Multicentrisk retikulohistiocytose er en sjælden form for paraneoplasi

Translated title of the contribution: Multicentric reticulohistiocytosis is a rare form of paraneoplasia

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.

Translated title of the contributionMulticentric reticulohistiocytosis is a rare form of paraneoplasia
Original languageDanish
JournalUgeskrift for Laeger
Volume180
Pages (from-to)2-3
Number of pages2
ISSN0041-5782
Publication statusPublished - 1 Jan 2018

Fingerprint

Dive into the research topics of 'Multicentric reticulohistiocytosis is a rare form of paraneoplasia'. Together they form a unique fingerprint.

Cite this