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العنوان
liver biopsy in diffuse interstitial pulmonary fibrosis
المؤلف
Gomaa, Magdy Abdel Salam El Saied
هيئة الاعداد
باحث / مجدى عبد السلام السيد جمعة
مشرف / عادل جمعة على
مشرف / حسين على حسين
مشرف / فوزى نجيب جرجس
تاريخ النشر
1993
عدد الصفحات
223 ص.
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
جراحة
تاريخ الإجازة
1/1/1993
مكان الإجازة
جامعة عين شمس - كلية الطب - امراض صدرية
الفهرس
Only 14 pages are availabe for public view

from 223

from 223

Abstract

Diffuse interstitial pulmonary fibrosis is defined as a condition of
unknown and possibly multiple causation characterized pathologically by a
diffuse in:flanunatory process in the lung beyond the terminal bronchioles
having its essential features:
1- Cellular thickening of the alveolar wall with a tendency to fibrosis.
2- The presence oflarge mononuclear cells within the alveolar spaces (1 ).
In the early stages of diffuse interstitial pulmonary fibrosis Pa 02 may
be normal at rest but falls on exercise when the alveolar-arterial oxygen
tension gradient is increased. With progression of disease, resting
hypoxaemia develops (2).
Owing to their active and complex metabolism, liver cells are readily
injured by hypoxia (3).
The serum levels of glutamic transaminases, lactic dehydrogenase and
alkaline phosphatase are raised in patients with COPD (4). Needle liver
biopsy performed in patients with COPD and resting hypoxaemia showed
focal necrosis and round cell infiltration of the portal tracts (5).