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Updated: Feb 18, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
[Chronic histiocytic intervillositis: Diagnosis and management]
A Mekinian1, N Costedoat-Chalumeau2, L Carbillon3
1Service de médecine interne, département inflammation immunopathologie, biothérapie Department (DHU i2B), hôpital Saint-Antoine, AP-HP, université Paris 6, 75012 Paris, France.
Abstract:
Chronic intervillositis is a rare condition, which is associated with severe obstetrical outcome and high recurrence rate. Obstetrical adverse events are intrauterine growth restriction, recurrent early miscarriages, intrauterine deaths and prematurity by placental insufficiency. The determination of the extension and the intensity of the chronic intervillositis are not currently standardized. High rates of recurrence have been described, but actually there is no reliable predictive biomarker. No treatment is currently validated, but the use of immunomodulatory drugs could be justified by the possible autoimmune or allo-immune origin. The treatment should be particularly discussed in patients with recurrent and severe obstetrical adverse events and in the presence of severe and massive histological lesions.
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