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(Chest. 1973;64:459-464.)
© 1973 American College of Chest Physicians

Interstitial Pulmonary Fibrosis and von Recklinghausen's Disease. An Ultrastructural and Immunofluorescent Study

Arthur S. Patchefsky M.D.1; William G. Atkinson M.D.1; Willis S. Hoch M.D.1; Gloria Gordon B.S.1; and Herman I. Lipshitz M.D.1

1 Thomas Jefferson University Hospital, Philadelphia, Pa.

We present the clinical and pathologic findings in a 28-year-old white woman with pulmonary fibrosis and von Recklinghausen's disease. Ultrastructural examination of a lung biopsy specimen showed increased collagen in the alveolar wall, associated with hyperplasia of granular pneumocytes. Large numbers of intraalveolar cells, morphologically suggestive of macrophages, but having tight junctions similar to epithelial cells were also present. Direct immunofluorescent examination using goat anti IgG, IgM, IgA, compliment, albumin, and fibrinogen failed to show specific fluorescence. Despite certain structural similarities to other familial and idiopathic forms of interstitial pneumonja, the pathogenesis remains poorly understood.

Submitted on March 2, 1973
Accepted on April 3, 1973




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[Abstract] [Full Text] [PDF]




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