Villonodular synovitis (pigmented)

pigmented villonodular synovitis: Pigmented villonodular synovitis (PVNS) is a rare benign proliferative disorder of the synovial membrane primarily affecting young adults (with a peak age of onset in the second to fourth decade of life) characterized by proliferative, locally invasive tumor-like lesions, usually involving a single joint, tendon sheath or bursae (most commonly the joints of the knee and hip and rarely others such as the ankle, shoulder and temporomandibular joints). It presents with pain and limitation of motion along with swelling, heat and tenderness over the involved joint, eventually leading to arthritic degeneration and significant locomotor deficit, if left untreated. PVNS can recur in patients even after treatment.

Endpoint definition

FinnGen phenotype data
diagram bullet diagram downward connector

Filter registries Inpat., Oupat., Death

Hospital Discharge: ICD-10 M12.2
Hospital discharge: ICD-9 7192
Cause of death: ICD-10 M12.2
Cause of death: ICD-9 7192

Check pre-conditions None

Include endpoints None

Check conditions None

Apply sex-specific rule None

diagram downward connector M13_VILLONODULAR

Extra metadata

Level in the ICD hierarchy 4
First used in FinnGen datafreeze DF2
Parent code in ICD-10 M12
Name in latin Synovitis villonodularis [pigmentata]

Summary Statistics

Key figures

All Female Male
Number of individuals 141 91 50
Unadjusted prevalence (%) 0.05 0.06 0.04
Mean age at first event (years) 40.97 40.83 41.22

Mortality

Follow-up Absolute risk HR [95% CI] p N
1998–2019 - - - -
15 years - - - -
5 years - - - -
1 year - - - -

Correlations

Index endpoint: M13_VILLONODULAR – Villonodular synovitis (pigmented)
GWS hits: 0

Survival analyses between endpoints

Plot

before Villonodular synovitis (pigmented)
after Villonodular synovitis (pigmented)

loading spinner Loading survival analyses plot

Drugs most likely to be purchased after Villonodular synovitis (pigmented)