History
Cole[5] has described 4 clinical stages of ainhum.
- In the first stage, a small clavus or callus develops on the medial aspect of the plantar fold of a toe (usually the fifth) that progresses to a narrow groove or fissure. This groove deepens and slowly encircles the toe. Progression may be slow and can develop first in childhood. The deepening of the fissure is associated with pain in 78% of patients but is less intense than pain in the third stage.
- The second stage is shorter because the toe becomes globular distal to the groove, which is associated with arterial narrowing and bone resorption.
- In the third stage, the bone separates at the joint with hypermotility of the toe. Pain may be intense.
- The fourth stage is characterized by a bloodless autoamputation of the toe at the site of the encircling band.
Physical
The clinical presentation depends on the stage to which the ainhum has progressed.
- The initial sign of a painful fissure under a toe may not be defining, but the progressive constriction at the base of the toe with distal edema is diagnostic of ainhum.
- The toe may become rotated, clawed, and dorsiflexed at the metatarsophalangeal joint.
- Ultimately, before the toe is shed, it may be attached by an increasingly slender thread of fibrous tissue.
- The clinical, histologic, and radiographic appearances in pseudoainhum are similar or identical to true ainhum.
Causes
In 1952, Wells and Robinson[6] proposed 4 distinct sources of annular constrictions of the digits. The sources include (1) annular scarring from frostbite, burns, or trauma, (2) true ainhum, (3) constricting bands that simulate ainhum, and (4) congenital bands.
The exact etiology of true ainhum is unclear. Race and climate apparently are predisposing factors. Ainhum also may have a genetic component, since ainhum has been reported to occur within families. Infection and walking barefoot in childhood are linked to ainhum but probably are not major factors in its development. Abnormal scarring does not appear to be a cause; ainhum and keloid formation rarely occur in the same individual.
Pseudoainhum may be acquired or congenital.
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