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高氨血症:多发性骨髓瘤中脑病的罕见病因。

Hyperammonemia: An Unusual Cause of Encephalopathy in Multiple Myeloma.

作者信息

Dayal Aneal S, Roy Moni, Chatterjee Tulika

机构信息

Internal Medicine, University of Illinois College of Medicine Peoria, Peoria, USA.

出版信息

Cureus. 2025 Aug 21;17(8):e90707. doi: 10.7759/cureus.90707. eCollection 2025 Aug.

Abstract

Multiple myeloma (MM) is a malignancy of plasma cells that commonly presents with kidney dysfunction, hypercalcemia, bone pain, and anemia. Although many patients exhibit these symptoms, other, less obvious presentations can complicate the prognosis. In this case report, we describe a 65-year-old African American female with known IgG Kappa MM, who initially presented with back pain - a common symptom associated with bone involvement in MM. However, during her hospital stay, she developed a profoundly altered mental status, which was later linked to elevated ammonia levels. Hyperammonemia is a rare but highly fatal complication in MM. Thus, all providers must be able to clinically recognize and understand how to potentially treat hyperammonemic encephalopathy in MM early in its course.

摘要

多发性骨髓瘤(MM)是一种浆细胞恶性肿瘤,通常表现为肾功能不全、高钙血症、骨痛和贫血。尽管许多患者有这些症状,但其他不太明显的表现会使预后复杂化。在本病例报告中,我们描述了一名65岁的非裔美国女性,已知患有IgG κ型MM,最初表现为背痛——这是MM中与骨受累相关的常见症状。然而,在她住院期间,她出现了严重的精神状态改变,后来发现这与氨水平升高有关。高氨血症在MM中是一种罕见但极具致命性的并发症。因此,所有医疗人员必须能够在临床中识别并了解如何在高氨血症性脑病病程早期对MM患者进行潜在治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbaf/12450278/e535b06778e6/cureus-0017-00000090707-i01.jpg

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