Pinto A, Hwang W S, McLeod D R, Moscowitz W, Lachman R S, Rimoin D L
Department of Pathology, Faculty of Medicine, University of Calgary, Alberta, Canada.
Arch Pathol Lab Med. 1993 Mar;117(3):322-5.
This article describes an unusual skeletal dysplasia in a male fetus diagnosed by ultrasound at 18 weeks of gestation. The clinical and radiologic findings resemble thanatophoric dysplasia. Histologic examination revealed abnormalities in the resting cartilage, physeal growth plate, and bone. The resting cartilage contained peculiar large chondrocytes with huge lacunae. The growth plate revealed absence of column formation and hypertrophic vacuolated chondrocytes extending far into the metaphyseal bone trabeculae. The bone was hypercellular with absence of lamellar bone. The cortical bone was scanty and woven. The histopathologic features are, therefore, unique and differ from all other well-recognized varieties of short-limbed platyspondylic dwarfism.
本文描述了一名男性胎儿在妊娠18周时经超声诊断出的一种罕见骨骼发育异常。临床和放射学表现类似于致死性骨发育不全。组织学检查显示静止软骨、生长板和骨骼存在异常。静止软骨含有特殊的大软骨细胞,伴有巨大的陷窝。生长板显示无柱状结构形成,肥大的空泡化软骨细胞延伸至干骺端骨小梁深处。骨骼细胞过多,无板层骨。皮质骨稀少且呈编织状。因此,组织病理学特征独特,与所有其他公认的短肢扁平椎侏儒症类型不同。