Introduction. Desmoid-type fibromatosis (DF) is a benign but locally
infiltrative soft tissue tumor that develops from fascia and
musculoaponeurotic tissue with high local recurrence rate. The aim of this
article was to present a case of recurrent desmoid-type fibromatosis of the
chest wall and chest wall reconstruction after tumor resection. Case
outline. A 62-year-old man came for an examination due to a tumor localized
on the right anterior chest wall. The patient undergone surgical excision of
desmoid-type fibromatosis of the abdominal wall one year ago. Physical
examination found a firm and painless 6-7 cm mass on the right side of the
chest wall with no swelling of superficial lymph nodes. Computed tomography
scan revealed a homogenous mass of soft tissue density, measuring 7.12 ?
4.23 cm, arising from right anterolateral wall of thoracic cage with
adjoining ribs destruction. The patient was taken for the operation and
right thoracotomy was done with excision of tumor along with resection of
8th, 9th and 10th ribs. The results of pathological examination were
consistent with the frozen section, and the patient was diagnosed with DF.
Despite the absence of postoperative radiotherapy, there was no evidence of
local recurrence two years later. Conclusion. Surgical treatment of
recurrent desmoid-type fibromatosis of the chest wall requires a wide
resection with negative margins. Multidisciplinary approach in case of
full-thickness defect of the chest wall and combination of pedicled muscle
flap and polypropylene mesh are important to provide chest wall stability.