Axillary web syndrome after axillary dissection
Section snippets
Methods
The senior author (REM) maintained a personal database of 750 consecutively treated or clinically evaluated breast cancer patients over the 16-year period 1980 to 1996. Review of this database revealed 44 patients with the signs and symptoms of AWS. In each of the 44 cases, the medical record was obtained, reviewed, and abstracted. Additionally, our surgical oncology group observed 4 patients who developed AWS after SLND for staging of early breast cancer. These charts were also obtained,
Physical characteristics of axillary web
The defining characteristic of this syndrome is a visible web of axillary skin overlying palpable cords of tissue that are made taut and painful by shoulder abduction (Fig. 1). The web is always present in the axilla and extends into the medial ipsilateral arm, frequently down to the antecubital space, and occasionally to the base of the thumb. Typically, there are two or three taut, tender, nonerythematous cords of tissue under the skin. Notably, the axillary web is neither immediately
Comments
Axillary web syndrome is a self-limited process that developed in 6% of the patients with invasive breast cancer treated by a single surgeon over a 16-year period. Although patients who develop AWS were treated with nonsteroidal anti-inflammatory medications, physical therapy, and range-of-motion exercises, our data failed to demonstrate that the treatments shortened or changed the self-limited course of the syndrome. We identified no long-term sequelae of AWS. Eleven percent of AWS patients
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