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A Case of Fibroblast Growth Factor Receptor Fusion-Positive Intrahepatic Cholangiocarcinoma With Humoral Hypercalcemia of Malignancy
被引:1
|作者:
Chauhan, Aditya
[1
]
Likasitwatanakul, Pornlada
[2
]
Ahmed, Ammar
[1
]
Sibley, Shalamar D.
[1
,3
]
机构:
[1] Univ Minnesota, Sch Med, Dept Med, Div Endocrinol Diabet & Metab, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Med, Div Internal Med, Sch Med, Minneapolis, MN USA
[3] Minneapolis Vet Affairs Hlth Care Syst, Dept Endocrinol Diabet & Metab, Minneapolis, MN USA
关键词:
parathyroid hormone-related peptide;
parathyroid hormone;
hypercalcemia;
humoral hypercalcemia of malignancy;
cholangiocarcinoma;
HORMONE-RELATED PEPTIDE;
PARATHYROID-HORMONE;
CANCER;
D O I:
10.7759/cureus.58741
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Humoral hypercalcemia of malignancy (HHM) comprises the majority of cases with malignancy-related hypercalcemia and is mediated by elevated parathyroid hormone-related peptide (PTHrP). HHM is rare in cholangiocarcinoma and has been reported only in a few case reports and series. We report a case of a 63year-old male with a history of locally advanced fibroblast growth factor receptor (FGFR) fusion-positive intrahepatic cholangiocarcinoma who presented with recurrent HHM. The first episode of his hypercalcemia occurred 15 months after the initial diagnosis of cholangiocarcinoma and coincided with disease progression. The hypercalcemia was treated with zoledronic acid, and an FGFR inhibitor was started for the treatment of his malignancy. The second hypercalcemia episode occurred nine months later, with evidence of further disease progression. HHM is associated with poor clinical outcomes; a high index of suspicion should be present to identify and treat this complication in cases of cholangiocarcinoma promptly. With an increased understanding of the molecular alterations underlying cholangiocarcinoma, it will also be necessary to further evaluate its co-occurrence with HHM as the specific molecular alterations in this setting could lay the groundwork for targeted therapies and improve risk stratification for these patients.
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