Malignant mesothelioma in subjects with Marfan's syndrome and Ehlers-Danlos syndrome: Only an apparent association

被引:15
作者
Bisconti, M
Bisetti, A
Bidoli, P
机构
[1] Osped A Galateo, Div Pneumol 3, I-73047 Lecce, Italy
[2] Univ La Sapienza, Dipartimento Sci Cardiovasc & Resp, Rome, Italy
[3] Ist Nazl Tumori, I-20133 Milan, Italy
关键词
malignant mesothelioma; Marfan's syndrome; Ehlers-Danlos syndrome;
D O I
10.1159/000029493
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Malignant mesothelioma is a rare neoplasm which could be favored by an hereditary predisposing factor. So far, malignant mesothelioma have never been described in patients with hereditary diseases of the connective tissue. Here, we report some cases of mesothelioma affecting subjects who were not exposed to inhalation of asbestos. One of these subjects was affected by Ehlers-Danlos syndrome, whereas in two brothers, mesothelioma was associated with Marfan's syndrome. The observation of the same histologic subtype of mesothelioma in two brothers and the coexistence of two pathologic conditions of mesodermal origin indicate the presence of hereditary factors predisposing to the cancerogenic action of even small amounts of asbestos. Structural alterations of collagen and primary immunodeficiency may represent the host factor inducing development of the neoplasm. We conclude that the association between these rare disorders of the connective tissue and mesothelioma may not be coincidental, but could be the result of the exposition to small amounts of asbestos in predisposed individuals. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:223 / 228
页数:6
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