Infantile Systemic Hyalinosis or Juvenile Hyaline Fibromatosis?
Article first published online: 14 APR 2004
Volume 21, Issue 2, pages 154–159, March 2004
How to Cite
Urbina, F., Sazunic, I. and Murray, G. (2004), Infantile Systemic Hyalinosis or Juvenile Hyaline Fibromatosis?. Pediatric Dermatology, 21: 154–159. doi: 10.1111/j.0736-8046.2004.21214.x
- Issue published online: 14 APR 2004
- Article first published online: 14 APR 2004
Abstract: Infantile systemic hyalinosis and juvenile hyaline fibromatosis are presumably autosomal recessive inherited diseases of unknown origin in which accumulation of an amorphous, hyaline material occurs in the skin and other organs. Both disorders may show clinical overlapping, suggesting that they might represent different variants of the same disease spectrum. We describe a 6-year-old boy with such overlap. Salient features included papular skin lesions on his face and neck, gingival hyperplasia, perianal nodules, large subcutaneous tumors on the scalp, hyperpigmented plaques over the metacarpophalangeal joints and malleoli, limited joint movement, diffuse osteopenia, short stature, and persistent diarrhea. Histopathologic and ultrastructural studies confirmed the presence of hyalin material in the dermis. The term systemic hyalinosis involves both conditions and should be preferred until a clear distinction can be made between them.