| Literature DB >> 23337098 |
Bangkim Chandra Khangembam1, Sellam Karunanithi, Punit Sharma, Krishan Kant Agarwal, Abhinav Singhal, Varun Singh Dhull, Chandrasekhar Bal, Rakesh Kumar.
Abstract
Proteus syndrome is an extremely rare genetic disorder characterized by an asymmetrical overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. We present a case of a six-year-old boy with proteus syndrome who underwent bone scintigraphy for suspected osteomyelitis. Bone scintigraphy ruled out osteomyelitis and suggested cellulitis. In addition, it demonstrated striking characteristic deformities, which need to be emphasized. Knowledge of these findings will avoid misinterpretation of bone scintigraphy in patients with proteus syndrome.Entities:
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Year: 2013 PMID: 23337098 DOI: 10.5152/dir.2013.081
Source DB: PubMed Journal: Diagn Interv Radiol ISSN: 1305-3825 Impact factor: 2.630