Severe multiple cartilaginous exostoses - A case report.
نویسندگان
چکیده
منابع مشابه
Severe Multiple Cartilaginous Exostoses
Multiple cartilaginous exostoses (MCE) is one of the most common inherited skeletal disorders. A collection of 1124 cases was reported by Stock and Barrington (1925). Recently other large series have been published by Solomon (1963) and Sauer (1979). Different terms have been used for it such as multiple exostoses, hereditary multiple exostoses and diaphyseal aclasis. The swelling or "lump" are...
متن کاملMultiple cartilaginous exostoses and development of chondrosarcomas--a systematic review.
INTRODUCTION Hereditary multiple cartilaginous exostoses is a syndrome characterised by the development of multiple osteochondromas. The diagnosis is typically made around the age of 12 years, and the prevalence is estimated at 1:50,000. During skeletal growth, the osteochondromas are benign, but in adult life malignant transformation into chondrosarcomas can occur. METHODS This study was a l...
متن کاملAcetabular dysplasia associated with hereditary multiple exostoses. A case report.
Hereditary multiple exostoses is an autosomal dominant disorder characterised by multiple osteochondromata, most commonly affecting the forearm, knee and ankle. Osteochondromata of the proximal femur have been reported to occur in 30% to 90% of affected patients with coxa valga in 25%. Acetabular dysplasia is rare but has been described. This is the first report of a patient requiring surgical ...
متن کاملHereditary multiple exostoses: report of a kindred.
In a large family with 37 members with multiple exostoses, only one person has developed sarcomatous degeneration of a lesion. Our review of published reports revealed great variation in the incidence of malignancy in multiple exostoses (10 to 25%). Most studies had sampling errors leading to the apparent overstatement of risk. In large pedigrees with essentially complete ascertainment of affec...
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ژورنال
عنوان ژورنال: The Kurume Medical Journal
سال: 1988
ISSN: 0023-5679,1881-2090
DOI: 10.2739/kurumemedj.35.117