Gemnani Rinkle, Gaidhane Shilpa A, Yelne Pallavi, Kadu Ajinkya, Karwa Vineet
Department of Medicine, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Cureus. 2024 Aug 16;16(8):e66979. doi: 10.7759/cureus.66979. eCollection 2024 Aug.
Immune thrombocytopenic purpura (ITP) patients typically exhibit mild mucocutaneous bleeding. Although corpus luteum hemorrhage (CLH) is usually asymptomatic, it can rarely result in serious intraperitoneal bleeding, usually in patients with coagulation abnormalities. In cases of severe thrombocytopenia, hemoperitoneum during ovulation during an ITP flare-up is an extremely unusual and potentially fatal event. Our patient, a 25-year-old multiparous female with a known case of ITP, presented with a spontaneous petechial rash all over the body, abdominal pain, and dizzy spells. Hemoglobin was 6.3 g/L with a platelet count of 0.04 × 10/L and a negative urine pregnancy test. An abdominopelvic ultrasound revealed free fluid in the peritoneal cavity, and a contrast-enhanced computed tomography (CECT) confirmed hemoperitoneum with a ruptured ovarian cyst. We report the case of a young female with ITP relapse who landed into massive intraperitoneal hemorrhage and was managed conservatively with platelet transfusion, steroids, and romiplostim.
免疫性血小板减少性紫癜(ITP)患者通常表现为轻度的黏膜皮肤出血。虽然黄体出血(CLH)通常无症状,但极少情况下会导致严重的腹腔内出血,通常发生在有凝血异常的患者中。在严重血小板减少的情况下,ITP发作期间排卵时出现腹腔积血是极其罕见且可能致命的事件。我们的患者是一名25岁的经产妇,已知患有ITP,出现全身自发性瘀点皮疹、腹痛和头晕。血红蛋白为6.3 g/L,血小板计数为0.04×10⁹/L,尿妊娠试验阴性。腹部盆腔超声显示腹腔内有游离液体,增强计算机断层扫描(CECT)证实为腹腔积血伴卵巢囊肿破裂。我们报告了一例ITP复发的年轻女性患者,该患者发生了大量腹腔内出血,并通过血小板输注、类固醇和罗米司亭进行保守治疗。