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以胸腔积液为表现的免疫球蛋白E(IgE)介导的多发性骨髓瘤

Immunoglobulin E (IgE)-Mediated Multiple Myeloma Presenting as Pleural Effusion.

作者信息

Nisar Sarah, Ur Rehman Anees, Khan Adil, Wahab Noor, Shah Syed Safiullah

机构信息

Internal Medicine, Khyber Medical College, Peshawar, PAK.

Medicine, Ayub Medical College, Peshawar, PAK.

出版信息

Cureus. 2023 Sep 22;15(9):e45802. doi: 10.7759/cureus.45802. eCollection 2023 Sep.

Abstract

Multiple myeloma (MM) is a disease characterized by the abnormal production of plasma cells. These plasma cells have the property to produce immunoglobulins (Ig), on the basis of which MM can be classified. Immunoglobulin G is responsible for most of the cases, while IgE mediates the rarest form of MM. Since the first case was reported in 1967, knowledge regarding IgE-mediated MM is based on individual case reports. Based on the information available, it is thought that IgE-mediated MM presents clinically with the involvement of renal, bone, and hematological symptoms, which are the same as any other myeloma. However, the MM rarely involves the pleura, leading to malignant pleural effusion. We present a case of IgE-mediated MM with a unique feature of pleural effusion. The patient presented with constitutional symptoms of MM, which were followed by lab investigations revealing low hemoglobin, hypercalcemia, and high creatinine levels. An incidental computed tomography angiography (CTA) revealed lytic lesions in the spine. This was followed by skull and chest X-rays as part of the workup to determine the extent of the disease. It revealed further lytic lesions in the skull, humerus, and scapula, along with pleural effusion. This led to the suspicion of MM, which was ultimately confirmed by serum protein electrophoresis and a bone marrow biopsy. The patient was started on a triple regimen of bortezomib, thalidomide, and dexamethasone, which led to substantial improvement in his symptoms.

摘要

多发性骨髓瘤(MM)是一种以浆细胞异常产生为特征的疾病。这些浆细胞具有产生免疫球蛋白(Ig)的特性,基于此可对MM进行分类。大多数病例由免疫球蛋白G引起,而IgE介导的MM最为罕见。自1967年首例病例报告以来,关于IgE介导的MM的认识均基于个别病例报告。根据现有信息,认为IgE介导的MM临床上表现为肾脏、骨骼和血液系统症状,与其他骨髓瘤相同。然而,MM很少累及胸膜,导致恶性胸腔积液。我们报告一例具有胸腔积液独特特征的IgE介导的MM病例。患者出现MM的全身症状,随后实验室检查显示血红蛋白低、高钙血症和肌酐水平高。偶然的计算机断层血管造影(CTA)显示脊柱有溶骨性病变。随后进行头颅和胸部X线检查,作为确定疾病范围的检查的一部分。检查发现头颅、肱骨和肩胛骨有进一步的溶骨性病变,同时伴有胸腔积液。这引发了对MM的怀疑,最终通过血清蛋白电泳和骨髓活检得以确诊。患者开始接受硼替佐米、沙利度胺和地塞米松的三联治疗方案,其症状有了显著改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb45/10591024/4a90bb3cc8fe/cureus-0015-00000045802-i01.jpg

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