Anderson K A, Burbach J A, Fenton L J, Jaqua R A, Barlow J F
Arch Pathol Lab Med. 1985 Sep;109(9):838-42.
We report two cases of idiopathic arterial calcification of infancy (IACI) occurring in newborn siblings. Unusual gross and light microscopic findings included calcification of multiple nonarterial tissues, renal infarction, and macroscopic aortic involvement. One case manifested an extensive acute panarteritis suggesting that IACI may be the result of an inflammatory or infectious process. Ultrastructural examination confirmed that the mineral deposits were hydroxyapatite and also indicated that they contained iron. Calcified tissue components included smooth-muscle cells, fibroblasts, and collagen fibers, as well as elastic fibers. No matrix vesicles or mitochondrial calcifications that may serve as nucleation sites for crystalline calcium phosphate were identified. Thus, the mechanism of calcification in IACI may be unique, and may relate to altered iron metabolism.
我们报告了两例发生在新生兄弟姐妹中的婴儿特发性动脉钙化(IACI)病例。不寻常的大体和光镜检查结果包括多个非动脉组织的钙化、肾梗死和主动脉肉眼可见的受累。其中一例表现为广泛的急性全动脉炎,提示IACI可能是炎症或感染过程的结果。超微结构检查证实矿物质沉积为羟基磷灰石,还表明它们含有铁。钙化的组织成分包括平滑肌细胞、成纤维细胞、胶原纤维以及弹性纤维。未发现可能作为磷酸钙晶体成核位点的基质小泡或线粒体钙化。因此,IACI中的钙化机制可能是独特的,可能与铁代谢改变有关。