Department of Rheumatology, Rennes University Hospital, Rennes 1 University, 35000, Rennes, France.
Department of Hepato-Gastroenterology, Saint-Brieuc Hospital, 22000, Saint-Brieuc, France.
Rheumatol Int. 2022 Jun;42(6):1105-1112. doi: 10.1007/s00296-021-04828-0. Epub 2021 Mar 11.
Calcium pyrophosphate deposition (CPPD) can be induced by a persistent hypomagnesemia. Tacrolimus is an immunosuppressive treatment especially used in organ transplant, potentially inducer of hypomagnesemia by renal loss. A 53-year-old man, liver transplant 10 months earlier, developed an acute peripheral oligoarthritis of wrist, hip and elbow with fever, associated with acute low back pain. Synovial fluid was sterile, and revealed calcium pyrophosphate crystals. Spinal imaging showed inflammatory changes. Magnesium blood level was low at 0.51 mmol/l, with high fractional excretion in favor of renal loss. Tacrolimus was changed for everolimus, proton pump inhibitor was stopped, and magnesium oral supplementation was started. After 8 months follow-up and slow prednisone tapering, he did not relapse pain. Persistent hypomagnesemia is a rare secondary cause of CPPD. In this entity, drug liability should be investigated such as tacrolimus in organ transplant patient.
焦磷酸钙沉积症(CPPD)可由持续低镁血症引起。他克莫司是一种免疫抑制剂,尤其用于器官移植,可能通过肾脏丢失导致低镁血症。一名 53 岁男性,肝移植术后 10 个月,出现腕、髋和肘的急性寡关节炎伴发热,伴有急性下腰痛。关节液无菌,可见焦磷酸钙晶体。脊柱影像学显示炎症改变。血镁水平低至 0.51mmol/L,肾小管重吸收镁分数高提示肾性丢失。将他克莫司换为依维莫司,停用质子泵抑制剂,开始口服补充镁。随访 8 个月,逐渐减少泼尼松剂量后,患者未再出现疼痛复发。持续性低镁血症是 CPPD 的罕见继发性病因。在这种情况下,应调查药物相关性,如器官移植患者使用他克莫司。