The enigmatic tale of parsonage-turner syndrome
An intricate case study unveiling diagnostic puzzles and therapeutic insights
Keywords:
enigmatic tale, parsonage-turner syndrome, unveiling diagnostic puzzles, therapeutic insightsAbstract
Neuralgic Amyotrophy, commonly referred to as Parsonage-Turner Syndrome (PTS), stands as a clinically diagnosed yet frequently overlooked inflammatory ailment that primarily targets the brachial plexus. [1] Regrettably, accurate identification of the condition is often delayed, subjecting patients to significant morbidity characterized by excruciating pain, muscle weakness, and sensory abnormalities in the upper extremity. Although the underlying pathophysiological mechanisms remain partially elusive, PTS typically emerges following a discernible triggering event, while the road to complete recovery can span from months to even years. [2] Within this context, we present a compelling case of PTS, aiming to shed light on the intricacies of the disease and foster heightened awareness to mitigate the risks associated with its under-diagnosis.
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