Download full-text PDF |
Source |
|---|
Publication Analysis
Top Keywords
Similar Publications
[Effect of surgery of pulmonary cysts related to immunoglobulin light chain deposits].
Rev Mal Respir
February 2020
Service de pneumologie, centre hospitalier de Luxembourg, Strassen, Luxembourg.
Introduction: Light chain deposition disease is a rare anatomo-clinical disorder, which rarely leads to cystic lung destruction.
Case Report: We report the case of a 62years old female patient with a history of a monoclonal gammopathy of unknown significance who developed progressive dyspnea. Thoracic CT-scan demonstrated a diffuse pulmonary cystic disorder with predominance in the right lower lobe.
[Renal involvement in Behçet's disease. About six cases].
Rev Med Interne
January 2003
Service de néphrologie, CHU Ibn Rochd, Casablanca, Maroc.
Purpose: To analyze anatomoclinic and evolutive aspects of the renal involvement associated to the Behçet's disease through 6 observations collected in the nephrology department from 1985 to 2000 and to make a review of the literature.
Methods: Retrospective study, diagnosis of Behçet's disease according to the Classification of the International Group Study on the Behçet's disease and renal damage confirmed by histology.
Results: Our patients all male are aged between 25 to 55 years with a mean at 34 years old.
[Vascular dementias].
Ann Radiol (Paris)
June 1994
Service de Neurologie, Hôpital Saint-Antoine, Paris.
The recent development of neuro-imaging technology has altered the classic anatomo-clinical pattern of vascular dementias (VD). However, few correlative studies have emerged and the creation of new eponyms--such as the successful "leuko-araiosis"--did not raise new highlights on the mechanisms involved in VD. The different clinical and radiological aspects of VD are briefly reviewed and the contribution of CT-scan and MRI are discussed.
View Article and Find Full Text PDF[Postmortem diagnosis of cardiac amyloidosis in the aged. Anatomoclinical correlation].
Arch Mal Coeur Vaiss
March 1993
The absence of specific clinical signs makes the diagnosis of cardiac amyloidosis difficult. Moreover, it is established that this condition, the prevalence of which increases with age, aggravates the prognosis of cardiac failure. The present study was undertaken to identify the clinical or paraclinical signs enabling more accurate diagnosis of this disease.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!