Fist hand deformity
Introduction
Introduction Boxing hand deformity is a series of deformed severely distorted or deformed deformities that occur after hand burns: twisted, fist-shaped and crippled. Loss of hand function. The back side of the hand is weaker, so the burns are deeper, often occurring at the same time as the face, or as part of a multi-site or large-area burn. Treatment should pay great attention to early treatment, in an effort to preserve hand function. Advanced treatments are organized according to the specific conditions of tissue transplantation, in an effort to maximize the recovery of the hand's labor function.
Cause
Cause
Malformation caused by hand burns.
Examine
an examination
Related inspection
X-ray lipiodol angiography blood routine hand deformity examination
an examination:
1. History of hand burns;
2. The shape of the hand deformed is different: the hypertrophic scar on the back of the hand, the claw-shaped hand, the twisted hand, the fist-like hand, etc.;
3. The degree of dysfunction varies;
4. X-ray film confirmed the deformation of bone and joint.
Diagnosis
Differential diagnosis
Differential diagnosis of fist-shaped hand deformity:
1. The deformity of the hand: The deformity of the hand is a clinical manifestation of the hand and foot hyperkinesia in involuntary movement.
2, intramuscular muscle atrophy: movement and sensory examination of the ruler syndrome, the small finger and ring finger ulnar side of the palm face sensory abnormalities and hand muscle atrophy.
3, "hands" deformity: skeletal muscle atrophy in the hand of the interosseous muscle, large and small intermuscular muscle atrophy, the formation of hand deformity. Peronial myoatrophy, also known as Charcot-Marie-Tooth disease (CMT), is the most common group of peripheral neuropathies, accounting for approximately 90% of all hereditary neuropathies. The common features of this group of diseases are the onset of children or adolescents, chronic progressive sacral muscle atrophy, and the symptoms and signs are relatively symmetrical. Most patients have a family history. Because of the main clinical features of iliac muscle atrophy, it is also known as peroneal myoatrophy. According to neurophysiological and neuropathological findings, CMT is classified into type I and type II, CMTI type is called hypertrophic type, and type CMTII is called neuronal type.
