Cyclic Fevers in Pregnancy: A Case of Parvovirus-Related Hemophagocytic Lymphohistiocytosis.

IF 0.8 Q4 OBSTETRICS & GYNECOLOGY
Case Reports in Obstetrics and Gynecology Pub Date : 2026-06-10 eCollection Date: 2026-01-01 DOI:10.1155/crog/7218689
Dominick J Rich, Meridith P Pollie, Julie P Barbera, Jordan S Stone, Adi Hirshberg
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引用次数: 0

Abstract

Parvovirus B19 typically causes mild symptoms in healthy adults, including fever, rash, and arthralgias. Certain immunocompromised adult populations, including those with immunodeficiencies or hematologic disease, are at risk of clinically significant complications, including transient aplastic crisis. Further, in pregnant patients, there is a risk of transplacental viral transmission, which may lead to severe fetal anemia, nonimmune hydrops fetalis, and intrauterine fetal demise. The clinical course of parvovirus B19 in pregnant patients with underlying hematologic disease has not been well reported. In this case report, we present a 27-year-old pregnant patient with sickle cell beta thalassemia who was infected with parvovirus B19 at 20 weeks of gestation. She experienced a prolonged hospitalization characterized by persistent maternal vaso-occlusive crisis with concomitant transient aplastic crisis. There was suspected vertical transmission of the virus, leading to concern for severe fetal anemia and termination of the pregnancy. The patient continued to have cyclic fevers, bicytopenia, and a constellation of laboratory findings leading to a diagnosis of postviral hemophagocytic lymphohistiocytosis (HLH). She was successfully treated with pulse dose corticosteroids and an Interleukin-1 receptor antagonist with subsequent improvement of her symptoms and laboratory markers. This report highlights the distinct diagnostic and management challenges of parvovirus B19 in pregnant patients with comorbid hematologic disease, including a rare but serious sequela of the infection, and the risk for severe maternal and fetal complications.

妊娠期周期性发热:一例细小病毒相关的噬血细胞淋巴组织细胞增多症。
细小病毒B19通常在健康成人中引起轻微症状,包括发烧、皮疹和关节痛。某些免疫功能低下的成年人,包括那些有免疫缺陷或血液病的人,有临床显著并发症的风险,包括短暂的再生危机。此外,在怀孕患者中,存在经胎盘病毒传播的风险,这可能导致严重的胎儿贫血、非免疫性胎儿水肿和宫内胎儿死亡。妊娠合并基础血液病的患者中细小病毒B19的临床病程尚未得到很好的报道。在这个病例报告中,我们提出了一个27岁的怀孕患者镰状细胞β地中海贫血谁是在妊娠20周感染细小病毒B19。她经历了长时间的住院治疗,其特征是持续的母体血管闭塞危机与伴随的短暂性再生危机。该病毒疑似垂直传播,导致对严重胎儿贫血和终止妊娠的担忧。患者持续出现周期性发热、双环白血球减少症和一系列实验室检查结果,诊断为病毒后噬血细胞淋巴组织细胞增多症(HLH)。她成功地接受了脉冲剂量皮质类固醇和白细胞介素-1受体拮抗剂治疗,随后她的症状和实验室标志物得到改善。本报告强调了合并血液病的妊娠患者中细小病毒B19的独特诊断和管理挑战,包括罕见但严重的感染后遗症,以及严重的母婴并发症风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Obstetrics and Gynecology
Case Reports in Obstetrics and Gynecology Medicine-Obstetrics and Gynecology
CiteScore
1.30
自引率
0.00%
发文量
64
审稿时长
12 weeks
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