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Literature DB >> 8677152

Neonatal osteofibrous dysplasia: report of two cases.

B W Hindman¹, S Bell, T Russo, C W Zuppan.

Abstract

Skeletal neoplasms of the newborn and neonatal period are infrequently encountered and often misdiagnosed. Osteofibrous dysplasia is a tumor of childhood that may be seen in the newborn. Because of its unique natural history, with and without surgical treatment, and the similarity in radiographic appearance of this tumor to other lesions, a high index of suspicion must be maintained when a tibial lesion is encountered in the newborn. We present two additional cases of neonatal osteofibrous dysplasia and discuss the differential diagnostic considerations.

Entities: Disease

Mesh：

Year: 1996 PMID： 8677152 DOI： 10.1007/bf01372118

Source DB: PubMed Journal: Pediatr Radiol ISSN： 0301-0449

12 in total

Neonatal osteofibrous dysplasia: report of two cases.

1. Solitary unicameral bone cyst in a seven-week-old infant.

2. Neurilemmona of bone. Report of 3 cases with a review of the literature.

3. Osteofibrous dysplasia in the newborn. Report of a case.

4. Disseminated nonossifying fibromas in association with café-au-lait spots (Jaffe-Campanacci syndrome).

5. Osteofibrous dysplasia of long bones a new clinical entity.

6. [Fibrous dysplasia of long bones with remission. Apropos of 3 cases].

7. Primary bone tumours in infants. Short literature review and report of 10 cases.

8. Solitary congenital fibromatosis (infantile myofibromatosis) of bone.

9. Case report 189. Infantile fibrosarcoma (congenital fibrosarcoma-like fibromatosis).

10. Osteofibrous dysplasia of the tibia and fibula.

1. Osteofibrous dysplasia: A rare case in 3-day-old female.