Juvenile hypertrophic osteoarthropathy associated with primary sclerosing cholangitis
โ Scribed by Antonio J. Reginato; Robert Petrokubi; C. Alan Jasper
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 479 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0004-3591
No coin nor oath required. For personal study only.
โฆ Synopsis
Hypertrophic osteoarthropathy has rarely been reported in children (1). Chronic lung disease has been the most commonly reported association in those series described during the preantibiotic era (1,2). Congenital cyanotic heart disease, biliary atresia, liver cirrhosis, metastatic lung tumor, and idiopathic cases with familial aggregation have been also seen in childhood (1-3). In some cases, arthritis may be very prominent and closely simulate the clinical picture of juvenile rheumatoid arthritis (1,2).
Reported here is a unique case of a teenage boy with idiopathic sclerosing cholangitis and hypertrophic osteoarthropathy, an association not described in the literature reviewed. He presented with spiking fever, jaundice, splenomegaly, and symmetrical arthritis of elbows, wrists, knees, and ankles mimicking juvenile rheumatoid arthritis.
CASE REPORT
In good health until November 1976, this 16year-old congenitally deaf black male sought medical aid because of daily spiking fever of several weeks duration. Physical examination was remarkable for icterus,
๐ SIMILAR VOLUMES
Primary sclerosing cholangitis (PSC) is a chronic fibroinflammatory syndrome involving the biliary tract, often accompanied by inflammatory bowel disease (IBD). This syndrome is a prototype disease linking chronic inflammation to carcinogenesis. Indeed, PSC is associated with an increased risk of ch
Background: Primary sclerosing cholangitis (PSC) is well known as one of the extraintestinal manifestations of ulcerative colitis (UC). However, the prevalence of PSC in UC patients together with the clinical characteristics and outcomes of UC associated with PSC (UC-PSC) are not clear in Asians. #