Idiopathic pulmonary fibrosis historical perspective: Difference between revisions
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==Historical Perspective== | ==Historical Perspective== | ||
===Discovery=== | ===Discovery=== | ||
* In 1872, Von Buhl reported pulmonary histologic findings which included infiltration of the lung with fibroblasts and excessive connective tissue. Dr. Von buhl reported this cases as a desquamative pneumonia due to desquamation of the alveolar and bronchiolar epithelium. Dr. Von buhl also used the term chronic interstitial pneumonia for the chronic cases and he assumed the cause to be tuberculosis or syphilis.<ref name="pmid3315158">{{cite journal| author=Homolka J| title=Idiopathic pulmonary fibrosis: a historical review. | journal=CMAJ | year= 1987 | volume= 137 | issue= 11 | pages= 1003-5 | pmid=3315158 | doi= | pmc=1267422 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3315158 }}</ref> | * In 1872, Von Buhl reported pulmonary histologic findings which included infiltration of the lung with [[fibroblasts]] and excessive [[connective tissue]]. Dr. Von buhl reported this cases as a [[Desquamative interstitial pneumonia|desquamative pneumonia]] due to [[desquamation]] of the [[alveolar]] and [[bronchiolar epithelium]]. Dr. Von buhl also used the term chronic [[interstitial pneumonia]] for the chronic cases and he assumed the cause to be [[tuberculosis]] or [[syphilis]].<ref name="pmid3315158">{{cite journal| author=Homolka J| title=Idiopathic pulmonary fibrosis: a historical review. | journal=CMAJ | year= 1987 | volume= 137 | issue= 11 | pages= 1003-5 | pmid=3315158 | doi= | pmc=1267422 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3315158 }}</ref> | ||
* In 1898, Dr. Rindfleisch reported a case of a 40 year old man who presented with worsening cough and dyspnea which are related to idiopathic pulmonary fibrosis. Dr. Rindfleisch described a a small stiffed lungs and hypertrophied right ventricles. The lungs contained dense fibrous tissues with round cells. Dr. Rindfleisch used the term "Cirrhosis cystica pulmonum" for this case at that time. | * In 1898, Dr. Rindfleisch reported a case of a 40 year old man who presented with worsening [[cough]] and [[dyspnea]] which are related to idiopathic pulmonary fibrosis. Dr. Rindfleisch described a a small stiffed [[lungs]] and hypertrophied [[Right ventricle|right ventricles]]. The [[lungs]] contained dense fibrous tissues with round cells. Dr. Rindfleisch used the term "''Cirrhosis cystica pulmonum''" for this case at that time. | ||
* In 1907, Dr. Sandoz reported a case in twin sisters who presented also with worsening cough and dyspnea. Both cases had a hypertrophic right ventricle and small lungs with thickened bronchioli and dense interstitial tissue. Dr. Sandoz named this case as "Fetal bronchiectasis". | * In 1907, Dr. Sandoz reported a case in twin sisters who presented also with worsening [[cough]] and [[dyspnea]]. Both cases had a hypertrophic [[right ventricle]] and small [[lungs]] with thickened bronchioli and dense interstitial tissue. Dr. Sandoz named this case as "''Fetal bronchiectasis''". | ||
* In 1912, Dr. von Hansemann reported five cases with lung interstitial abnormalities in the histologic examination. Dr. von Hansemann named those cases as "lymphangitis reticularis pulmonum" . | * In 1912, Dr. von Hansemann reported five cases with lung interstitial abnormalities in the histologic examination. Dr. von Hansemann named those cases as "lymphangitis reticularis pulmonum" . | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
Pulmonary fibrosis was first dexcribed by Dr. Von Buhl in 1872. Dr. Rindfleish reported a case of a 40 year old patient who presented with worsening cough and dyspnea and he named this case as "Cirrhosis cystica pulmonum" in 1898.
Historical Perspective
Discovery
- In 1872, Von Buhl reported pulmonary histologic findings which included infiltration of the lung with fibroblasts and excessive connective tissue. Dr. Von buhl reported this cases as a desquamative pneumonia due to desquamation of the alveolar and bronchiolar epithelium. Dr. Von buhl also used the term chronic interstitial pneumonia for the chronic cases and he assumed the cause to be tuberculosis or syphilis.[1]
- In 1898, Dr. Rindfleisch reported a case of a 40 year old man who presented with worsening cough and dyspnea which are related to idiopathic pulmonary fibrosis. Dr. Rindfleisch described a a small stiffed lungs and hypertrophied right ventricles. The lungs contained dense fibrous tissues with round cells. Dr. Rindfleisch used the term "Cirrhosis cystica pulmonum" for this case at that time.
- In 1907, Dr. Sandoz reported a case in twin sisters who presented also with worsening cough and dyspnea. Both cases had a hypertrophic right ventricle and small lungs with thickened bronchioli and dense interstitial tissue. Dr. Sandoz named this case as "Fetal bronchiectasis".
- In 1912, Dr. von Hansemann reported five cases with lung interstitial abnormalities in the histologic examination. Dr. von Hansemann named those cases as "lymphangitis reticularis pulmonum" .