Gilliatt-Sumner Hand is a distinctive clinical entity observed in patients with neurogenic thoracic outlet syndrome (nTOS), characterized by progressive atrophy of the intrinsic hand muscles. This phenomenon reflects chronic compression of the lower trunk of the brachial plexus, leading to motor denervation and subsequent wasting of the thenar, interosseous, and hypothenar muscle groups. In the context of an orthopedic symposium, an in‐depth discussion of its clinical presentation, diagnostic workup, and treatment modalities is warranted.
A multimodal diagnostic approach is essential for accurate evaluation:
Initial management emphasizes conservative modalities:
Surgical Intervention
For progressive motor deficits:
Gilliatt-Sumner Hand represents a severe manifestation of neurogenic TOS. Early recognition and timely intervention—ranging from conservative management to surgical decompression—are critical to preventing irreversible motor deficits and optimizing patient outcomes.