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Abstract
The Journal of the Postgraduate Institute of Medicine (JPGIM) is an open access, peer-reviewed, biannual journal published by the Postgraduate Institute of Medicine (PGIM) of the University of Colombo (UOC), Sri Lanka. The JPGIM aims to publish articles relevant to clinicians, policymakers, and researchers on topics relating to the practice of medicine, medical education, professionalism, integrity, and ethics of the research enterprise. The JPGIM has been in publication since 2014 and publishes accepted manuscripts online immediately after copy-editing, enabling rapid dissemination of scientific knowledge. The published articles are compiled into two issues in June and December.The Journal practices a double-blind peer review policy. The JPIGM does not charge any article processing or publication fee.We recommend that you review the About the Journal page for the journal's section policies, as well as the Submission Guidelines. Authors need to register with the journal prior to submitting or, if already registered, can simply log in and begin the five-step process.
Highlights
Mixed connective tissue disease [MCTD] is a systemic autoimmune disease with features of systemic lupus erythematosis [SLE], systemic sclerosis and polymyositis/dermatomyositis along with positive anti-U1 ribonucleoprotein [RNP] antibodies [1].Here we report a case of an 18-year-old female presenting with menorrhagia and symptomatic anaemia, along with small joint pain, Raynaud’s phenomenon, alopecia with thrombocytopenia and positive anti-U1RNP antibodies which led to a diagnosis of MCTD with secondary ITP
We report a case of an 18-year-old female presenting with menorrhagia and symptomatic anaemia, along with small joint pain, Raynaud’s phenomenon, alopecia with thrombocytopenia and positive anti-U1RNP antibodies which led to a diagnosis of MCTD with secondary ITP
Even though secondary ITP is associated with autoimmune diseases, cases of MCTD with secondary ITP are rare [1,2]
Summary
Mixed connective tissue disease with secondary immune thrombocytopenic purpura - A case report.
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