Kozlowski K, Grigor W G
Pediatr Radiol. 1980;9(1):45-7. doi: 10.1007/BF00973971.
A 7-week-old infant who probably had congenital histiocytosis X of the Letterer-Siwe type, and who showed mesomelic involvement of the long bones, is reported. Although skeletal changes are common in histiocytosis of the Letterer-Siwe type, very early appearance and localisation of these changes is unusual.
报道了一名7周大的婴儿,可能患有勒-雪氏病(Letterer-Siwe type)先天性组织细胞增多症X型,且长骨出现四肢中部受累。虽然骨骼改变在勒-雪氏病型组织细胞增多症中很常见,但这些改变出现得非常早且局限并不常见。