Dirweesh Ahmed, Siddiqui Waqas, Khan Muhammad, Iyer Praneet, Seelagy Marc
Department of Internal Medicine, Seton Hall University School of Medicine, Saint Francis Medical Center, Trenton, NJ, USA.
Department of Nephrology, Drexel University College of Medicine, Philadelphia, PA, USA.
Respir Med Case Rep. 2017 Apr 6;21:82-83. doi: 10.1016/j.rmcr.2017.04.004. eCollection 2017.
Acquired thrombotic thrombocytopenic purpura (TTP) usually presents as severe microangiopathic hemolytic anemia (MAHA) and thrombocytopenia in a previously healthy individual. It occurs in approximately three in one million adults and 1 in 10 million children annually. The incidence is increased in females and blacks. Diagnosing TTP and initiating therapy with plasma exchange is a must to avoid preventable complications. Acquired thromotic microangiopathy has been linked to collagen vascular diseases, use of certain medications, organ transplants, infections, pregnancy and cancer. We report a rare case of a 56-year-old African American male diagnosed with TTP who found to have an asymptomatic adenocarcinoma of the lung. Prompt cancer management resulted in completed remission of the thrombotic microangiopathy.
获得性血栓性血小板减少性紫癜(TTP)通常表现为严重的微血管病性溶血性贫血(MAHA)和血小板减少,多见于既往健康的个体。其年发病率约为百万分之三的成年人和千万分之一的儿童。女性和黑人的发病率更高。诊断TTP并启动血浆置换治疗对于避免可预防的并发症至关重要。获得性血栓性微血管病与胶原血管疾病、某些药物的使用、器官移植、感染、妊娠和癌症有关。我们报告了一例罕见病例,一名56岁的非裔美国男性被诊断为TTP,同时发现患有无症状性肺腺癌。及时的癌症治疗使血栓性微血管病完全缓解。