Artigo Revisado por pares

Congenital Ewing's sarcoma of the humerus.

1998; Wiley; Volume: 71; Issue: 852 Linguagem: Inglês

10.1259/bjr.71.852.10319008

ISSN

1748-880X

Autores

Hsing-Fang Hsieh, Chih‐Cheng Hsiao, W S Chen, Jen‐Wei Lin, W J Chen, Y. Louise Wan, S.-H. Ng, T Y Lee, S F Ko,

Tópico(s)

Hematological disorders and diagnostics

Resumo

We report an extremely rare case of Ewing's sarcoma (ES) of the humerus in a Chinese neonate. Plain radiography and magnetic resonance imaging showed extensive neoplastic involvement of the humeral diaphysis and adjacent soft tissues, confirmed on histology and immunohistochemistry as being due to ES. This is the first report of congenital ES in a long bone. Since ultrasound at 20 weeks gestation showed a normal fetal skeleton, the ES may have begun to develop in the late middle or third trimester.

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