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一名复发的前B细胞急性淋巴细胞白血病成年患者的高钙血症和多发性溶骨性病变:病例报告

Hypercalcemia and multiple osteolytic lesions in an adult patient with relapsed pre-B acute lymphoblastic leukemia: a case report.

作者信息

Kaiafa G, Perifanis V, Kakaletsis N, Chalvatzi K, Hatzitolios A I

机构信息

First Propedeutic Department of Internal Medicine AHEPA University Hospital, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.

Department of Immunology, Laboratory of Microbiology, AHEPA University Hospital, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece.

出版信息

Hippokratia. 2015 Jan-Mar;19(1):78-81.

Abstract

BACKGROUND

Hypercalcemia and severe osteolytic lesions are rare complications of acute lymphoblastic leukemia (ALL) in childhood, and those cases share similar clinical features. Similarly, hypercalcemia is a rare feature in adult ALL. Here, we report an uncommon case of an adult patient with relapsed precursor B ALL (pre-B ALL) who developed multiple osteolytic lesions and hypercalcemia.

CASE DESCRIPTION

A 24-year-old male patient, diagnosed with pre-B ALL, was admitted in our hospital due to severe lumbar pain. After reviewing laboratory, radiological and clinical findings, the patient was diagnosed as having relapse of a mixed phenotype acute leukemia, according to bone marrow aspiration (9% blasts) and cytogenetic analysis, with multiple osteolytic lesions in all lumbar vertebrae, sacrum and ilium and severe hypercalcemia (13.3 mg/dL). Thus, FLAG-IDA rescue therapy and hydration plus furosemide, corticoids and bisphosphonates were administered. Despite initial amelioration, his hematological condition deteriorated and he died due to severe sepsis as a result of severe immunosuppression.

CONCLUSION

Two possible mechanisms have been suggested for hypercalcemia in hematological malignancy, either the leukemic infiltration or the paraneoplastic production of a variety of humoral factors and proinflammatory cytokines. However, hypercalcemia and severe osteolytic lesions are rare features in ALL adult patients and their combination may be indicator of poor prognosis. Hippokratia 2015, 19 (1): 78-81.

摘要

背景

高钙血症和严重溶骨性病变是儿童急性淋巴细胞白血病(ALL)罕见的并发症,这些病例具有相似的临床特征。同样,高钙血症在成人ALL中也是罕见特征。在此,我们报告一例成年复发性前体B-ALL(pre-B ALL)患者出现多处溶骨性病变和高钙血症的罕见病例。

病例描述

一名24岁男性患者,诊断为pre-B ALL,因严重腰痛入院。经实验室、影像学和临床检查,根据骨髓穿刺(原始细胞9%)和细胞遗传学分析,该患者被诊断为混合表型急性白血病复发,所有腰椎、骶骨和髂骨均有多处溶骨性病变且伴有严重高钙血症(13.3mg/dL)。因此,给予FLAG-IDA挽救治疗以及补液加呋塞米、皮质类固醇和双膦酸盐治疗。尽管最初病情有所改善,但由于严重免疫抑制导致严重脓毒症,其血液学状况恶化并最终死亡。

结论

血液系统恶性肿瘤中高钙血症的发生机制有两种可能,即白血病浸润或多种体液因子和促炎细胞因子的副肿瘤性产生。然而,高钙血症和严重溶骨性病变在成年ALL患者中较为罕见,二者并存可能提示预后不良。《希波克拉底》2015年,第19卷(1):78 - 81页。

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