R. Rodriguezjurado et al., PROGRESSIVE OSSEOUS HETEROPLASIA, UNCOMMON CAUSE OF SOFT-TISSUE OSSIFICATION - A CASE-REPORT AND REVIEW OF THE LITERATURE, PEDIATRIC PATHOLOGY & LABORATORY MEDICINE, 15(5), 1995, pp. 813-827
We report a case of an uncommon, recently described disease manifestin
g shortly after birth, characterized by extensive soft tissue calcific
ation with ossification, progressive osseous heteroplasia. We describe
the complex histopathologic patterns present in this case, discuss th
e main differential diagnoses that the surgical pathologist must consi
der when confronted by soft tissue ossification, and review the pertin
ent literature. We conclude that although the morphologic patterns of
ossification in progressive osseous heteroplasia are complex and the i
nvolvement is extensive, the morphology of the lesions lacks diagnosti
c specificity. The diagnosis must be based on a consideration of the c
ombined clinical data and radiologic and pathologic findings. This app
roach alone makes it possible to exclude a number of clinicopathologic
entities that manifest with so-called osteoma cutis but whose associa
ted lesions and genetic implications are different.