Nishimura G, Iwasawa T, Fukuzawa R, Hirabayashi Y, Ito T
Department of Radiology, Dokkyo University School of Medicine, Tochigi, Japan.
Clin Dysmorphol. 1998 Jul;7(3):195-200. doi: 10.1097/00019605-199807000-00007.
We report the radiological and histological findings of another case of platyspondylic lethal chondrodysplasia. The patient was a girl, who died of respiratory failure at 18 days of age. The radiological changes comprised moderate platyspondyly with ovoid-shaped vertebral bodies, broad and short ilia, rhizomelic shortening and mild bowing of the long bones (particularly of the humeri), relatively long short tubular bones, and retarded epiphyseal ossification and ragged metaphyses, which were most similar to those of a mild variant of this entity, the Luton type. However, the histological findings of cartilage, including hypercellularity of the reserve zone with round resting chondrocytes, relatively normal column formation of the proliferative and hypertrophic zones, and incorporation of hypertrophic cartilage with a columnar arrangement into metaphyseal bony trabeculae, resemble those of a severe variant of this entity, the Torrance type. Our observation provides an insight into the phenotypic variabilities of platyspondylic lethal chondrodysplasia.
我们报告了另一例扁平椎致死性软骨发育不良病例的放射学和组织学 findings。该患者为一名女孩,18 天时死于呼吸衰竭。放射学改变包括中度扁平椎,椎体呈椭圆形,髂骨宽而短,四肢近端短小,长骨(尤其是肱骨)轻度弯曲,短管状骨相对较长,骨骺骨化延迟且干骺端参差不齐,这些与该实体轻度变异型卢顿型最为相似。然而,软骨的组织学 findings,包括储备区软骨细胞增多且呈圆形静止状态,增殖区和肥大区柱状结构相对正常,以及呈柱状排列的肥大软骨融入干骺端骨小梁,与该实体严重变异型托伦斯型相似。我们的观察为扁平椎致死性软骨发育不良的表型变异性提供了见解。