2002
DOI: 10.1007/s100670200108
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Coexistence of Osteopoikilosis and Discoid Lupus Erythematosus: A Case Report

Abstract: Osteopoikilosis is an uncommon, benign sclerosing bone dysplasia characterised by typical roentgenographic findings and usually seen in patients with dermatological problems. We report a case of osteopoikilosis and discoid lupus erythematosus presenting with skin and mucosal involvement, an association that has never previously been reported. We also discuss the differential diagnosis and the clinical pathologies accompanying osteopoikilosis in the literature.

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Cited by 30 publications
(17 citation statements)
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“…Occasionally, this condition is associated with renal or heart malformations or endocrine disorders [1]. Several pathologies can coexist with OPK, such as rheumatoid arthritis, systemic lupus erythematosus, reactive arthritis, ankylosing spondylitis, psoriatic arthritis, familial Mediterranean fever, dacryocystitis, scleroderma, fibromyalgia, and Quervain's syndrome [1,2,4,[12][13][14][15]. Primarily asymptomatic OPK associated with connective tissue nevi of the skin is categorized as Buschke-Ollendorff syndrome (BOS).…”
Section: Discussionmentioning
confidence: 99%
“…Occasionally, this condition is associated with renal or heart malformations or endocrine disorders [1]. Several pathologies can coexist with OPK, such as rheumatoid arthritis, systemic lupus erythematosus, reactive arthritis, ankylosing spondylitis, psoriatic arthritis, familial Mediterranean fever, dacryocystitis, scleroderma, fibromyalgia, and Quervain's syndrome [1,2,4,[12][13][14][15]. Primarily asymptomatic OPK associated with connective tissue nevi of the skin is categorized as Buschke-Ollendorff syndrome (BOS).…”
Section: Discussionmentioning
confidence: 99%
“…It is commonly associated with small subcutaneous fibrous nodules called dermatofibrosis lenticularis disseminate (Buschke-Ollendorff syndrome) [1,2]. However, patients with osteopoikilosis and rheumatoid arthritis, polyarthralgia, synovial chondromatosis, dacriocystitis, trisomy 8, connective tissue disorders affecting the skin and joints, and discoid lupus erythematosus have also been reported [3,4,5,6,7,8,9]. Here we report a pediatric renal transplant recipient with amyloidosis secondary to familial Mediterranean fever (FMF) who was incidentally diagnosed as having osteopoikilosis in the 6th post-transplant year.…”
Section: Sirsmentioning
confidence: 98%
“…Reports have described cases of concurrent OPK and RA [9][10][11], as well as comorbidity involving RA and symptoms of Sjögren's syndrome [12], systemic lupus erythematosus [13], and discoid lupus erythematosus [14]. Osteopoikilosis is known to occur in association with symptoms of systemic sclerosis [15,16], keloid formation [7,16], and with seronegative spondyloartropathy [17,18].…”
Section: Discussionmentioning
confidence: 99%
“…Opisywano równoczesne występowanie OPK i RZS [9][10][11], a także RZS skojarzonego z objawami zespołu Sjögrena [12], tocznia rumieniowatego układowego [13] i tocznia rumieniowatego krążkowego [14]. Osteopoikilia łączyła się z objawami twardziny układowej [15,16], powstawaniem bliznowców [7,16] oraz ze spondyloartropatiami seronegatywnymi [17,18].…”
Section: Dyskusjaunclassified