Results 111 to 120 of about 288 (135)
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A Skeleton with Diaphyseal Aclasis
The South African Archaeological Bulletin, 1962openaire +3 more sources
Primary Osteoma Cutis and Diaphyseal Aclasis
Archives of Dermatology, 1962The following report describes a patient with bony nodules in the skin and a rare hereditary anomaly of bone. She was presented at a meeting of the North of England Dermatological Society in October, 1960, when none of those attending had seen a similar combination. Osteoma Cutis Osteoma cutis, the presence of true bone in the skin, is rare.
E M, DONALDSON, R, SUMMERLY
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Radionuclide bone imaging in diaphyseal aclasis with malignant change
Cancer, 1986Chondrosarcoma is a rare complication in hereditary multiple exostoses. The six patients in this study have had a complete follow-up and constitute the largest group of such cases to have been studied so far. Five patients had histologic evidence of malignancy. Since histologic examination can be very difficult, any other diagnostic features, may it be
J F, Bouvier +8 more
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Malignization of diaphyseal aclasis.
Diagnostic imaging, 19838 secondary chondrosarcomas in 7 patients with diaphyseal aclasia are reported. Effective diagnostic imaging is a key to early operative removal of the tumours. Angiography proved to be highly useful in tracing the malignant character and true extension of the lesion. Also skeletal nuclear investigations support the diagnosis.
J, Kolár +3 more
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Multiple Cartilaginous Exostoses (Diaphyseal Aclasis) in a Yorkshire Terrier
Journal of Small Animal Practice, 1968Abstract— Multiple cartilaginous exostoses of the left ileum, left scapula, thoracic vertebrae, and the ribs were seen in a 16‐month‐old female Yorkshire Terrier. The condition which resembled hereditary multiple exostoses in man, has been described in detail in the dog only once previously and insufficient evidence is available to implicate a ...
L. N. OWEN, S. W. NIELSEN
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Osteochondromatosis (diaphyseal aclasis): a case report and literature review.
The Journal of foot surgery, 1989An unusual case of osteochondromatosis is presented with a review of the literature. Osteochondromatosis, also known as hereditary multiple exostoses or diaphyseal aclasis, are inherited, benign, cartilaginous neoplasms that consist of a pedicle of normal bone covered with proliferating cartilage cells.
M D, Perlman, A D, Schor, M L, Gold
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Australian and New Zealand Journal of Obstetrics and Gynaecology, 1966
D, Adey, B, Kneale
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D, Adey, B, Kneale
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Some Features of a Case of Multiple Exostoses—Diaphyseal Aclasis (Keith)
Radiology, 1935The patient, G. B., an undersized man of 58 years, was admitted to the hospital suffering from cerebral concussion, the result of a motor accident. All limbs were greatly misshapen, and a later inquiry elicited the following facts. The patient was the youngest of a family of eleven children, none of whom showed any bony abnormalities.
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