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The Annals of Thoracic Surgery, Vol 25, 289-297, Copyright © 1978 by The Society of Thoracic Surgeons
ER Munnell, E Dilling, RN Grantham, MR Harkey and JA Mohr
Twelve patients with solitary bronchiolar carcinoma had lobectomy and were
followed for up to 16 years. The concept of a multicentric origin of
bronchiolar carcinoma, maintained for more than eight decades, should be
discarded. The neoplasm arises indolently and usually in an area of
pulmonary fibrosis. After lobectomy patients can now expect to follow one
of four courses: (1) to be alive and well without recurrence; (2) after
several years to have pulmonary recurrence or a new carcinoma; (3) with
minute spread at the time of lobectomy to have metastasis develop in a
short period; or (4) to die of unrelated conditions. The overall 5-year
survival with this tumor is about 75%. Late recurrence or the development
of another primary tumor, however, prompts the need for prolonged
follow-up. Immunologically, patients have circulating antibodies when well
and demonstrable circulating antigens with recurrence. The survival rate of
selected patients with solitary bronchiolar carcinoma (eliminating those
patients with microscopic spread from the primary neoplasm at the time of
resection and those dying of other causes) was 100% after 5 years and 75%
after 10 years.
ARTICLES
Reappraisal of solitary bronchiolar (alveolar cell) carcinoma of the lung
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