Fatal Granulomatosis of the Respiratory Tract (Lethal Midline Granuloma-Wegener's Granulomatosis)
Fatal Granulomatosis of the Respiratory Tract (Lethal Midline Granuloma-Wegener's Granulomatosis)
复制标题
呼吸道致命肉芽肿病(致命中线肉芽肿-韦格纳肉芽肿病)
DOI:
10.1001/archotol.1959.00730040721007
复制
发表时间:
1959
影响因子:
--
通讯作者:
W. Schull
中科院分区:
文献类型:
--
作者:
I. Blatt;H. Seltzer;P. Rubin;A. Furstenberg;J. Maxwell;W. Schull
Fatal granulomatosis of the respiratory tract is a disease with a noteworthy natural history, recognizable clinical manifestations, and identifying pathologic characteristics. Men, women, and children of all ages are susceptible, many of whom have no previous stigmata of allergic or vascular disease. The earliest reference to this disease appeared in 1897, when McBride1 1 reported bizarre ulcerative granulomatous lesions in "a case of rapid destruction of the nose and face." Similar cases have been reported by Fordyce, 2 Woods, 3 Falchi, 6 Chatellier, 7 Kraus, 8 Stewart, 13 and others. In 1936 and 1939, Wegener 26,27 published three cases characterized by necrotizing granulomatosis of the nose, nasal accessory sinuses, larynx, and lungs associated with a "peculiar granulomatous nephritis." Wegener believed that the nose was the primary site of the disease and applied the term "rhinogenous granulomatosis" to the disease process. A review of the available literature from 1897 to 1957