Unusual presentation of acquired thrombotic thrombocytopenic purpura (TTP) versus catastrophic antiphospholipid syndrome in a patient with Moya‐Moya disease, case report, and literature review

Author:

Guevara‐Rodriguez Nehemias1ORCID,Marmanillo‐Mendoza Gabriela1,Castelar Jorge1,Ciobanu Camelia1,Fulger Ilmana2

Affiliation:

1. Department of Medicine, Internal Medicine St. Barnabas Hospital Health System The Bronx New York USA

2. Department of Medicine, Internal Medicine, Department of Hemato‐Oncology St. Barnabas Hospital Health System The Bronx New York USA

Abstract

Key Clinical MessageCoincidences in medicine are not so common. We are presenting a case of a patient diagnosed with Moya‐Moya disease and antiphospholipid syndrome (APS) who presented with clinical and laboratory characteristics of catastrophic APS versus TTP. The diagnosis was a challenge because characteristics were overlapping. Nevertheless, a decision to treat the patient for TTP was made with afterward improvement. MMD has been associated with multiple immune disorders; however, only one case of acquired thrombotic thrombocytopenic purpura has been documented in association with this disease. None has been associated with catastrophic antiphospholipid syndrome. We are presenting a challenging case where all these three medical conditions were present at the same time.

Publisher

Wiley

Subject

General Medicine

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