Chronic Immune Thrombocytopenia and Hashimoto’s Hypothyroidism in an Adolescent: Presentation and Implications
Judy Ibrahim; Mohammad Alashqar; Shamma Al Zaabi; Omar Trad; Amar Al Shibli · 2021 · Case Reports in Pediatrics
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
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Abstract
Immune thrombocytopenia (ITP) is a disorder characterized by immune-mediated destruction of thrombocytes leading to peripheral blood platelet count of <100 × 10^9/L. Primary ITP is a terminology used in the absence of other causes or disorders that may be associated with thrombocytopenia, i.e., isolated thrombocytopenia. The term secondary ITP is used if such diseases coexist. We present here a case of a 14-year-old female diagnosed with immune thrombocytopenia. When her evaluation was not strongly supportive of primary ITP, she was screened and proved to have a concomitant Hashimoto thyroidit
Abstract by Judy Ibrahim; Mohammad Alashqar; Shamma Al Zaabi; Omar Trad; Amar Al Shibli, Case Reports in Pediatrics (2021) — licensed CC BY 4.0.
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Metadata source: DOAJ · DOI 10.1155/2021/6649155