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Osteogenic sarcoma associated with the Rothmund-Thomson syndrome

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

The Rothmund-Thomson syndrome (RTS), also called poikiloderma congenitale, is a rare autosomal recessive disorder characterized by photosensitivity, poikiloderma of the face and extremities, juvenile cataracts, skeletal abnormalities, and a higher incidence of malignancy. Presented is the case of a 6-year-old boy with RTS who developed an osteogenic sarcoma of the tibia. A bone scan showed bilateral radius agenesis and a hot bone lesion in the proximal tibia metaphysis. An incisional bone biopsy led to a diagnosis of osteogenic sarcoma. There is an association between RTS and osteosarcoma, and there should be a high index of suspicion when patients with RTS develop bony pain.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Page 116 (1 page)

Journal (Volume, Issue Number)

Clinical nuclear medicine (Volume 23, Issue 2)

Publication milestones

  • Published - 1998

Publication status

Published - 1998

ISSN

0363-9762

Publication IDs

  • Scopus: 0031891440
  • PubMed: 9481507

Publication metrics

Metrics

SciVal
citations
3
Scopus
citations
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
1
SciVal
FWCI
0.44
SciVal
Author count
3
SciVal
Paper percentile
41

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Citation count
5
Captures
1