Sarcoidosis is a systemic granulomatous disease involving multiple organs with predominantly pulmonary manifestations. Severe thrombocytopenia is a relatively rare hematologic manifestation of sarcoidosis. Immune thrombocytopenia is usually characterized by excessive antibody production leading to platelet destruction. There are a few reported cases of immune thrombocytopenic purpura secondary to sarcoidosis, but the pathophysiologic mechanism remains unknown. We report the case of a 65-year-old woman who presented severe thrombocytopenia and was found to have immune thrombocytopenic purpura secondary to sarcoidosis.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168564 | PMC |
http://dx.doi.org/10.26574/maedica.2022.17.1.234 | DOI Listing |
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