| Literature DB >> 29054902 |
Alexandra Daniel1, Gianluca Bagnato2, Edward Vital2, Francesco Del Galdo3.
Abstract
The authors present a case of a 51-year-old woman with clinical diagnosis of mixed connective tissue disease and overlap systemic lupus erythematosus features, with a 6-month history of progressive painless abdominal distension. On examination, evident signs of ascites were present. Both the abdominal-pelvic ultrasound and CT scan confirmed a large amount of ascites. A diagnostic paracentesis was performed, which revealed typical features of chylous ascites (CA). An extensive diagnostic work-up led by a multidisciplinary team was performed, excluding malignancy, cirrhosis, infectious, as well as cardiac and primary lymphatic causes. The patient was kept under surveillance, with dietary therapy and periodic ascitic drainages. The hypothesis of an autoimmune cause for CA was considered by exclusion. Rituximab therapy was initiated and an excellent response was achieved, with reduction of the rate of accumulation of CA and an increase in quality of life of the patient. © BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.Entities:
Keywords: biological agents; connective tissue disease; gastrointestinal system
Mesh:
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Year: 2017 PMID: 29054902 PMCID: PMC5665331 DOI: 10.1136/bcr-2017-222339
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X