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一种新发现的犬骨软骨瘤病模式。

A newly recognized pattern of canine osteochondromatosis.

作者信息

Mozos Elena, Novales Manuel, Ginel Pedro J, Pérez José, Pool Roy R

机构信息

Departamento de Anatomía y Anatomía Patológica Comparadas, Facultad de Veterinaria, Universidad de Córdoba, Spain.

出版信息

Vet Radiol Ultrasound. 2002 Mar-Apr;43(2):132-7. doi: 10.1111/j.1740-8261.2002.tb01660.x.

DOI:10.1111/j.1740-8261.2002.tb01660.x
PMID:11954808
Abstract

Clinicopathological findings are described for a unique skeletal pattern of osteochondromatosis (syn. multiple osteochondromas) in three crossbred littermate dogs. Multiple nonpainful bilaterally symmetric skeletal lesions arose from focal semiannular and annular areas of periosteal thickening on the cortical surface of the metaphyses and diaphyses of long bones. Flat bones of the skull were spared. In radiographs osteochondromas in different stages of evolution were apparent. Grossly there were smoothly contoured, nodular subperiosteal masses of dense fibrocartilaginous and osseous tissue that were continuous with and overlying apparently normal but thin trabeculae of cancellous bone. Cortical compacta was attenuated or absent beneath exostoses. In histologic sections of the cartilage-capped exostoses a hyperplastic periosteum formed a focal semiannular or annular cap of proliferative hyaline cartilage tissue that underwent endochondral ossification and replacement by cancellous bone at its base. Intertrabecular spaces in the cancellous bone of exostoses were filled with fibro-osseous and hematopoietic tissue. A hereditary origin was suspected for the osteochondromas. Origin of some osteochondromas as semiannular or annular perturbations of the perichondrial ring of metaphyseal physes of long bones likely contributed to limb shortening and a pattern of billaterally symmetric angular limb deformities of all limbs as occurs in some children affected by osteochondromatosis.

摘要

描述了三只杂交同窝犬中一种独特的骨软骨瘤病(同义词:多发性骨软骨瘤)骨骼模式的临床病理特征。多个无痛性双侧对称骨骼病变起源于长骨干骺端和骨干皮质表面骨膜增厚的局灶性半环形和环形区域。颅骨扁骨未受累。在X线片中,不同演变阶段的骨软骨瘤清晰可见。大体上,有轮廓光滑的结节状骨膜下肿块,由致密的纤维软骨和骨组织构成,与松质骨明显正常但较薄的小梁相连并覆盖其上。外生骨疣下方的皮质骨变薄或缺失。在软骨帽状外生骨疣的组织学切片中,增生的骨膜形成增生性透明软骨组织的局灶性半环形或环形帽,其在基部经历软骨内成骨并被松质骨替代。外生骨疣松质骨的小梁间隙充满纤维骨和造血组织。怀疑骨软骨瘤有遗传起源。一些骨软骨瘤起源于长骨干骺端生长板软骨膜环的半环形或环形扰动,这可能导致肢体缩短以及所有肢体出现双侧对称的角形肢体畸形模式,就像一些患骨软骨瘤病的儿童那样。

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