Majid Bushra, Ahmed Syed Hassan, Majid Hanifa
Dow University of Health Sciences, Karachi, Pakistan.
Ann Med Surg (Lond). 2022 Nov 5;84:104828. doi: 10.1016/j.amsu.2022.104828. eCollection 2022 Dec.
Post-partum TTP is an uncommon thrombotic microangiopathy affecting about 1 in 200,000 pregnancies in contrast to preeclampsia and HUS, which have been reported commonly.
We report a case of a postpartum TTP following purpureal sepsis. The patient was brought with per vaginal bleed, vomiting, chest pain, yellow discoloration of sclera, and abdominal discomfort following a spontaneous vaginal delivery two days back at a hospital.
The workup revealed anemia and thrombocytopenia with deranged PT/INR. The renal profile deteriorated over one day and she also developed psychosis. Additionally, schistocytes were observed on the peripheral blood smear.
The patient was subsequently treated with dialysis followed by plasmapheresis in addition to the antibiotics after the diagnosis of TTP and made a complete recovery.
25% of TTP occurs in the intra or postpartum period. It is thus pivotal to keep it among differentials and intervened timely to reduce morbidity and mortality. Vigilance is required to prevent any relapse in subsequent pregnancies.
产后血栓性血小板减少性紫癜(TTP)是一种罕见的血栓性微血管病,与常见报道的先兆子痫和溶血尿毒综合征(HUS)相比,其在每20万次妊娠中约有1例发生。
我们报告一例产后紫癜败血症后发生的TTP病例。该患者两天前在一家医院自然阴道分娩后,因阴道出血、呕吐、胸痛、巩膜黄染和腹部不适入院。
检查发现贫血、血小板减少,凝血酶原时间/国际标准化比值(PT/INR)异常。肾功能在一天内恶化,她还出现了精神错乱。此外,外周血涂片上观察到裂红细胞。
诊断为TTP后,患者随后接受了透析治疗,继之进行血浆置换,并使用了抗生素,最终完全康复。
25%的TTP发生在孕期或产后。因此,将其纳入鉴别诊断并及时干预以降低发病率和死亡率至关重要。后续妊娠需要保持警惕以防止任何复发。