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[Secretan's syndrome: myth or pathomimia?]
S Collet1, A Forli2, P-H Carpentier1
1Clinique de médecine vasculaire, clinique universitaire de médecine vasculaire, CHU de Grenoble, BP 217, 38043 Grenoble cedex 09, France.
Secretan's syndrome is a rare condition causing hand edema, often due to self-inflicted trauma. Diagnosis can be challenging, requiring awareness among vascular medicine physicians.
Area of Science:
- Vascular Medicine
- Dermatology
- Psychiatry
Background:
- Secretan's syndrome is a rare condition characterized by hard edema on the dorsal hand, typically following trauma.
- The etiology is poorly understood, with factitious trauma frequently suspected.
Observation:
- A case report details a 42-year-old woman with unexplained hand edema and pain, unresponsive to extensive imaging.
- Diagnostic challenges arise from the atypical presentation and the exclusion of organic causes.
Findings:
- The diagnosis of Secretan's syndrome was established based on clinical presentation and the exclusion of other conditions.
- Three forms—benign, hyperplastic, and mixed—have been described, with pathomimia suggested as a cause.
Implications:
- Secretan's syndrome may be underdiagnosed due to its rarity and complex diagnosis.
- Increased physician awareness, particularly in vascular medicine, is crucial for timely diagnosis and management.
- Treatment may involve physiotherapy and psychological support.
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