Kozlowski K, Barylak A, Eftekhari F, Pasyk K, Wislocka E
Pediatr Radiol. 1979 Apr 19;8(2):79-86. doi: 10.1007/BF00973996.
Four cases of idiopathic acroosteolysis are reported. The first is a common phalangeal type, the second, the Hozay variety. The third case was diagnosed after a mumps infection, and marked regress of the changes was noted in the following years. The fourth case shows skin changes, periostitis, mild osteosclerosis, and skull changes as well as acroosteolysis.
报告了4例特发性肢端骨质溶解症。第一例为常见的指骨型，第二例为霍扎伊型。第三例在腮腺炎感染后确诊，随后几年观察到病变明显消退。第四例表现为皮肤改变、骨膜炎、轻度骨硬化、颅骨改变以及肢端骨质溶解。
