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以高钙血症为表现的弥漫性大B细胞淋巴瘤

Diffuse Large B-Cell Lymphoma Presenting With Hypercalcemia.

作者信息

Hegazy Yasser, Chung Mike, Zamora Nicholas, Lee Heng-Tien Aaron, Ghallab Muhammad

机构信息

Internal Medicine, Icahn School of Medicine at Mount Sinai, Queens Hospital Center, New York, USA.

Internal Medicine, The New York Institute of Technology College of Osteopathic Medicine, New York, USA.

出版信息

Cureus. 2024 Nov 13;16(11):e73642. doi: 10.7759/cureus.73642. eCollection 2024 Nov.

Abstract

Hypercalcemia is a common metabolic complication associated with malignancies, particularly in solid tumors, such as lung and breast cancers. However, its occurrence in hematologic malignancies, including diffuse large B-cell lymphoma (DLBCL), is rare. The pathophysiology of hypercalcemia in lymphomas is often related to the secretion of parathyroid hormone (PTH)-related peptide (PTHrP). However, an alternative and less common mechanism involves the ectopic overproduction of 1,25-dihydroxyvitamin D (1,25(OH)2D), which has been reported in some cases of lymphoma-associated hypercalcemia. In this case report, we present a 60-year-old female who was incidentally found to have hypercalcemia during the evaluation of nonspecific symptoms, ultimately leading to the diagnosis of DLBCL with liver and splenic involvement. The patient presented to the emergency department with symptoms of shortness of breath, palpitations, insomnia, polydipsia, and polyuria. Laboratory evaluation revealed a critical calcium level of 12.5 mg/dL, along with suppressed PTH levels and elevated 1,25(OH)2D levels, suggesting an ectopic source of 1-alpha-hydroxylase activity. Imaging revealed hepatic and splenic masses, and a liver biopsy confirmed the diagnosis of DLBCL. Further evaluation ruled out more common causes of hypercalcemia, such as osteolytic metastases and PTHrP-related mechanisms, reinforcing the likelihood that the patient's hypercalcemia was due to ectopic 1,25(OH)2D production. This case underscores the complexity of hypercalcemia in patients with DLBCL, particularly when uncommon mechanisms such as ectopic 1,25(OH)2D synthesis are involved. While the exact etiology of hypercalcemia in DLBCL remains incompletely understood, it is emerging as a potential biomarker for poor prognosis. Studies suggest that hypercalcemia in DLBCL may correlate with aggressive disease features, shorter diagnosis-to-treatment intervals, and worse overall outcomes. In this case, the patient's hypercalcemia may reflect the biological aggressiveness of her disease, with a relatively short interval to treatment after diagnosis. Further research is necessary to better understand the prognostic significance of hypercalcemia in DLBCL and its underlying mechanisms.

摘要

高钙血症是一种与恶性肿瘤相关的常见代谢并发症,在实体瘤中尤为常见,如肺癌和乳腺癌。然而,它在血液系统恶性肿瘤中发生,包括弥漫性大B细胞淋巴瘤(DLBCL),却很罕见。淋巴瘤中高钙血症的病理生理学通常与甲状旁腺激素(PTH)相关肽(PTHrP)的分泌有关。然而,另一种不太常见的机制涉及1,25 - 二羟维生素D(1,25(OH)2D)的异位过度产生,这在一些淋巴瘤相关高钙血症病例中已有报道。在本病例报告中,我们介绍了一名60岁女性,在评估非特异性症状时偶然发现高钙血症,最终诊断为累及肝脏和脾脏的DLBCL。患者因呼吸急促、心悸、失眠、多饮和多尿症状就诊于急诊科。实验室检查显示血钙水平高达12.5 mg/dL,同时甲状旁腺激素水平降低,1,25(OH)2D水平升高,提示存在1-α-羟化酶活性的异位来源。影像学检查发现肝脏和脾脏有肿块,肝脏活检确诊为DLBCL。进一步评估排除了高钙血症更常见的原因,如溶骨性转移和PTHrP相关机制,进一步证实患者高钙血症是由于异位产生1,25(OH)2D所致。该病例强调了DLBCL患者高钙血症的复杂性,特别是当涉及异位1,25(OH)2D合成等不常见机制时。虽然DLBCL中高钙血症的确切病因仍未完全了解,但它正逐渐成为预后不良的潜在生物标志物。研究表明,DLBCL中的高钙血症可能与侵袭性疾病特征、较短的诊断至治疗间隔以及较差的总体预后相关。在本病例中,患者的高钙血症可能反映了其疾病的生物学侵袭性,诊断后至治疗的间隔相对较短。有必要进行进一步研究,以更好地了解DLBCL中高钙血症的预后意义及其潜在机制。

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