Department of Internal Medicine, School of Medicine, Istanbul Medipol University, Istanbul, Türkiye.
Hematology Department, Çam Sakura City Hospital, Istanbul, Türkiye.
BMC Infect Dis. 2024 Oct 24;24(1):1201. doi: 10.1186/s12879-024-10074-z.
Pneumocystis jirovecii pneumonia (PJP) is an opportunistic infection that primarily affects immunocompromised individuals. Typical symptoms of PJP include the subacute onset of dyspnea, nonproductive cough, and low-grade fever. In hematology patients, particularly those who are allogeneic stem cell transplant recipients, the disease often presents with a more aggressive clinical course. While hypercalcemia has been documented as a manifestation of PJP in some solid organ transplant recipients, it has not been reported in hematology or stem cell transplant patients.
Here, we present a case of PJP in a 56-year-old male allogeneic stem cell transplant recipient, who developed hypercalcemia and renal failure during the late post-transplant period. The patient had a history of allogeneic stem cell transplantation due to acute myeloid leukemia. He presented with symptoms of fatigue and weakness. Laboratory tests revealed hypercalcemia (13.8 mg/dL) and elevated serum creatinine levels (2.3 mg/dL). The patient was hospitalized, and despite initial treatment with hydration and furosemide, the hypercalcemia persisted, leading to the administration of denosumab. During follow-up, hypoxia was detected, and a chest CT scan revealed mosaic attenuation and ground-glass opacities. Bronchoscopy was performed, and PCR testing confirmed the presence of Pneumocystis jirovecii. Other causes of hypercalcemia were ruled out, with PTH measured at 13.8 pg/mL (normal range 15-65 pg/mL), albumin at 3.71 g/dL, 1.25-dihydroxy vitamin D3 at 96 ng/dL (normal range 26-95 ng/dL), and 25-hydroxy vitamin D at 32.5 ng/mL (normal range 20-40 ng/mL). A PET-CT scan demonstrated no pathological FDG uptake, with the exception of findings suggestive of a pulmonary infection. Following treatment with trimethoprim-sulfamethoxazole and denosumab, the patient's hypercalcemia and infection resolved.
Although rare, PJP can present with hypercalcemia and kidney injury in allogeneic stem cell transplant recipients. Early diagnosis and treatment can improve both PJP and hypercalcemia.
肺孢子菌肺炎(PJP)是一种机会性感染,主要影响免疫功能低下的个体。PJP 的典型症状包括亚急性发作的呼吸困难、无痰咳嗽和低热。在血液系统疾病患者中,特别是异基因干细胞移植受者,疾病常呈现更具侵袭性的临床过程。虽然高钙血症已被记录为一些实体器官移植受者 PJP 的表现,但在血液系统或干细胞移植患者中尚未报道。
这里,我们报告了一例 56 岁男性异基因干细胞移植受者的 PJP 病例,该患者在移植后期发生高钙血症和肾衰竭。该患者因急性髓系白血病行异基因干细胞移植。他表现出疲劳和虚弱的症状。实验室检查显示高钙血症(13.8mg/dL)和血清肌酐水平升高(2.3mg/dL)。患者住院治疗,尽管最初接受水化和呋塞米治疗,但高钙血症持续存在,随后给予地舒单抗治疗。在随访过程中,发现患者缺氧,胸部 CT 扫描显示马赛克衰减和磨玻璃样混浊。行支气管镜检查,PCR 检测证实存在肺孢子菌。排除了其他高钙血症的原因,甲状旁腺激素(PTH)测量值为 13.8pg/mL(正常范围 15-65pg/mL),白蛋白为 3.71g/dL,1.25-二羟维生素 D3 为 96ng/dL(正常范围 26-95ng/dL),25-羟维生素 D 为 32.5ng/mL(正常范围 20-40ng/mL)。PET-CT 扫描除了提示肺部感染的发现外,未见病理性 FDG 摄取。接受甲氧苄啶-磺胺甲恶唑和地舒单抗治疗后,患者的高钙血症和感染得到缓解。
尽管罕见,但 PJP 可导致异基因干细胞移植受者出现高钙血症和肾脏损伤。早期诊断和治疗可改善 PJP 和高钙血症。