妊娠早期嗜血细胞淋巴组织细胞增多症:罕见而致命的诊断难题。

IF 0.5 Q4 OBSTETRICS & GYNECOLOGY
Jose Rojas-Suarez, María Ramos, Isabel Lazarte, Sofia Cifuentes, Jorge Leon, Wendy Castañeda, Karen Morales, Yasaira Pajaro, Carmelo Dueñas-Castell
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引用次数: 0

摘要

目的:本报告详细介绍了诊断和治疗妊娠期多系统噬血细胞淋巴组织细胞病(HLH)的复杂性,并以一例妊娠早期伴有严重血液学和产科并发症的死亡病例为证据。病例介绍:一名20岁的孕妇,第二次怀孕,在妊娠8周时出现腹痛、发烧和直肠出血。实验室检查显示白细胞减少,血小板减少和贫血,导致立即输血和重症监护病房入住。尽管进行了包括血管加压剂和抗生素在内的强化干预,患者还是出现了进行性器官衰竭,伴有弥漫性血管内凝血,并发生了致命的中风。结论:这一伴有严重并发症的危重病例显示了妊娠早期快速发作的HLH的诊断和治疗挑战。产科急诊的早期和准确鉴别诊断对于高肝炎等疾病至关重要。本病例强调了在管理具有复杂、非典型表现的妊娠患者时,多方面护理的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hemophagocytic lymphohistiocytosis in early pregnancy: A rare and fatal diagnostic challenge.

Objective: This report details the complexities of diagnosing and treating rapid-onset multisystemic hemophagocytic lymphohistiocytosis (HLH) during pregnancy, as evidenced by a fatal case in early pregnancy with severe hematological and obstetric complications.

Case presentation: A 20-year-old pregnant woman in her second pregnancy presented at 8 weeks of gestation with abdominal pain, fever, and rectal bleeding. Laboratory tests revealed leukopenia, thrombocytopenia, and anemia, leading to immediate transfusion and intensive care unit admission. Despite intensive interventions, including vasopressors and antibiotics, the patient developed progressive organ failure, with disseminated intravascular coagulation, and suffered a fatal stroke.

Conclusions: This critical case with severe complications demonstrates the diagnostic and treatment challenges of rapid-onset HLH in early pregnancy. Early and accurate differential diagnosis in obstetric emergencies is vital for conditions such as HLH. This case highlights the importance of multifaceted care in managing pregnant patients with complex, atypical presentations.

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来源期刊
Obstetric Medicine
Obstetric Medicine OBSTETRICS & GYNECOLOGY-
CiteScore
1.90
自引率
0.00%
发文量
60
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