Objectives: A retrospective study of primary chest wall tumors (PCWTs/CWTs)
was conducted to review their clinical, radiological and pathological feat
ures, as well as the early and long-term results of surgical management. Ma
terials and methods: From 1986 through 1996, 41 patients (18/44% male, 23/5
6% female, aged 15-78 years) with PCWTs were treated in our department. Res
ults: Twenty-three patients (nine male, 14 female, mean age 36 years) had a
benign CWT: enchondroma, five patients; fibrous dysplasia, four patients;
neurilemoma, three patients; osteochondroma, two patients; granular cell tu
mor, two patients; fibroma, two patients; lipoma, two patients; fibrolipoma
, one patient; eosinophilic granuloma, one patient; aneurysmal bone cyst, o
ne patient. Eighteen patients (nine male, nine female, mean age 59 years) h
ad a malignant CWT: plasmacytoma, five patients; chondrosarcoma, two patien
ts; osteosarcoma, two patients; fibrosarcoma, two patients; desmoid tumor,
two patients; leiomyosarcoma, one patient; malignant fibrous histiocytoma,
one patient; tendon sheath sarcoma, one patient; hemangiosarcoma, one patie
nt; neurinosarcoma, one patient. The ribs were involved in 21 patients, the
sternum in five patients, and the soft tissue in 17 patients. Distinction
between benign and malignant CWT was not possible using radiographic criter
ia alone, and diagnosis was always confirmed histologically. Surgical treat
ment consisted of wide resection in 29 patients (15 benign/14 malignant CWT
s), with the use of synthetic mesh in five cases, and excisional or incisio
nal biopsy in 12 patients. There was no perioperative mortality. Two patien
ts with a benign CWT (fibroma, one patient; neurilemoma, one patient) had a
local recurrence at 13 and 26 months after resection, respectively, and un
derwent wide resection (recurrence rate 8.7%). Follow-up at 3-13 years reve
aled one non-tumor-related death in patients with benign CWT (overall morta
lity rate 4.3%) and no other local recurrence. The overall 5- and 10-year s
urvival in patients with malignant CWT was 33.3%. Conclusions: We believe t
hat all CWTs should be considered malignant until proven otherwise. Wide re
section with tumor-free margins is required in order to provide the best ch
ance for cure in both benign and malignant lesions. (C) 2001 Elsevier Scien
ce B.V. All rights reserved.