Osteogenic sarcoma associated with the Rothmund-Thomson syndrome
- K. J. Macura(corresponding author),
- G. Burke,
- Medical College of Georgia,
Scholary Output:
Contribution to journal
Article
Peer-reviewAbstract
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-reviewOriginal 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
0363-9762Publication IDs
- Scopus: 0031891440
- PubMed: 9481507
Publication metrics
Metrics
SciVal
citations
3
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
PlumX, opens in new tab
Citation count
5
Captures
1
