Abstract |
Cranial fasciitis is a rare, rapidly growing, but benign fibroblastic tumor of the skull that generally presents in childhood. Local resection or curettage of the affected bone is generally curative and the tumor is thought not to recur. Cranial fasciitis is distinguished by positive cytoplasmic and nuclear beta-catenin staining. Fibromatosis is a clonal myofibroblastic nonmalignant proliferation that generally demonstrates positive nuclear beta-catenin staining. In this report, the authors present a patient with fibromatosis with cranial fasciitis characteristics in a 2.5-month-old boy who has had 7 recurrences (total 8 resections) of this fibroblastic neoplasm over 6 years of follow-up.
|
Authors | Rui Dai, Irene J Pien, David A Brown, Andre Marshall, Herbert E Fuchs, Jeffrey R Marcus |
Journal | The Journal of craniofacial surgery
(J Craniofac Surg)
Vol. 28
Issue 7
Pg. 1821-1823
(Oct 2017)
ISSN: 1536-3732 [Electronic] United States |
PMID | 28885439
(Publication Type: Case Reports, Journal Article)
|
Chemical References |
|
Topics |
- Cell Nucleus
(metabolism, pathology)
- Child
- Cytoplasm
(metabolism, pathology)
- Fasciitis
(complications, surgery)
- Fibroma
(complications, metabolism, pathology, surgery)
- Follow-Up Studies
- Humans
- Immunohistochemistry
- Male
- Neoplasm Recurrence, Local
(pathology, surgery)
- Skull Neoplasms
(complications, metabolism, pathology, surgery)
- beta Catenin
(metabolism)
|