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妊娠期多发性骨髓瘤的异常表现:一例报告

An Abnormal Presentation of Multiple Myeloma in Pregnancy: A Case Report.

作者信息

Chory Robert M, Cone Ryan, Hollingsworth Joshua

机构信息

Obstetrics and Gynecology, Edward Via College of Osteopathic Medicine-Auburn, Auburn, USA.

Pharmacology, Edward Via College of Osteopathic Medicine-Auburn, Auburn, USA.

出版信息

Cureus. 2022 Mar 21;14(3):e23363. doi: 10.7759/cureus.23363. eCollection 2022 Mar.

Abstract

Multiple myeloma (MM) is an uncommon hematologic malignancy in the general population and extremely rare in pregnant and peripartum women. Here we report a rare case of multiple myeloma in a 43-year-old African American woman at 24 weeks gestation who presented for severe flank pain and difficulty breathing. An elevated D-dimer was present on initial presentation and diagnoses of deep vein thrombosis and pulmonary embolism were ruled out via bilateral Doppler ultrasounds and CT scan. Lytic bone lesions, anemia, and elevated total protein were also noted and an iliac crest biopsy demonstrating monoclonal plasma cells confirmed the diagnosis of MM. She was started on steroids at 27 weeks gestation and delivered via c-section at 30 weeks gestation. Postpartum, a treatment regimen to allow for breastfeeding was discussed but was unable to be accommodated, and she was started on a multi-drug chemotherapy regimen. There have only been about 30 cases of multiple myeloma in pregnant women reported in the literature. The rarity and lack of information on the effects of multiple myeloma in pregnancy was the primary indication for publication of this case.

摘要

多发性骨髓瘤(MM)在普通人群中是一种不常见的血液系统恶性肿瘤,在孕妇和围产期妇女中极为罕见。在此,我们报告一例罕见的多发性骨髓瘤病例,患者为一名43岁的非裔美国女性,妊娠24周,因严重的侧腹痛和呼吸困难前来就诊。初次就诊时D-二聚体升高,通过双侧多普勒超声和CT扫描排除了深静脉血栓形成和肺栓塞的诊断。还发现了溶骨性骨病变、贫血和总蛋白升高,髂嵴活检显示单克隆浆细胞,确诊为MM。她在妊娠27周时开始使用类固醇,并于妊娠30周时行剖宫产分娩。产后,讨论了允许母乳喂养的治疗方案,但未能实施,她开始接受多药化疗方案。文献中仅报道了约30例孕妇多发性骨髓瘤病例。多发性骨髓瘤在妊娠中的罕见性以及缺乏关于其影响的信息是发表本病例的主要原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/9020588/2035f42d1563/cureus-0014-00000023363-i01.jpg

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