Atypical presentation of PJP: hypercalcemia and kidney injury in an allogeneic stem cell transplant recipient.

IF 3.4 3区 医学 Q2 INFECTIOUS DISEASES
Yunus Can Özalp, Hajrij Shehabie, Mehmet Günhan Tekin, Süreyya Yiğit Kaya, Hüseyin Saffet Beköz, Senem Maral, Ömür Gökmen Sevindik, Leylagül Kaynar
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引用次数: 0

Abstract

Background: 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.

Case presentation: 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.

Conclusions:  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.

PJP 的非典型表现:异体干细胞移植受者的高钙血症和肾损伤。
背景:肺孢子虫肺炎(PJP)是一种机会性感染,主要影响免疫力低下的人群。PJP 的典型症状包括亚急性呼吸困难、无排泄性咳嗽和低烧。对于血液病患者,尤其是接受异体干细胞移植的患者,该病的临床表现通常更为凶险。虽然高钙血症是一些实体器官移植受者的 PJP 表现,但在血液科或干细胞移植患者中却未见报道:在此,我们介绍了一例 56 岁男性异体干细胞移植受者的 PJP 病例,该患者在移植后晚期出现了高钙血症和肾功能衰竭。患者曾因急性髓性白血病接受异基因干细胞移植。他出现了疲劳和虚弱的症状。实验室检查显示他患有高钙血症(13.8毫克/分升)和血清肌酐水平升高(2.3毫克/分升)。患者被送入医院,尽管最初使用了补液和呋塞米治疗,但高钙血症仍持续存在,因此需要使用地诺单抗。在随访期间,发现患者缺氧,胸部 CT 扫描发现马赛克衰减和磨玻璃不透明。患者接受了支气管镜检查,PCR 检测证实其体内存在肺孢子虫。排除了导致高钙血症的其他原因,测得PTH为13.8 pg/mL(正常范围15-65 pg/mL),白蛋白为3.71 g/dL,1.25-二羟维生素D3为96 ng/dL(正常范围26-95 ng/dL),25-羟维生素D为32.5 ng/mL(正常范围20-40 ng/mL)。PET-CT 扫描显示,除了提示肺部感染的结果外,没有病理 FDG 摄取。在接受三甲双胍-磺胺甲噁唑和地诺单抗治疗后,患者的高钙血症和感染症状消失: 结论:PJP虽然罕见,但可在异体干细胞移植受者中出现高钙血症和肾损伤。早期诊断和治疗可改善PJP和高钙血症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Infectious Diseases
BMC Infectious Diseases 医学-传染病学
CiteScore
6.50
自引率
0.00%
发文量
860
审稿时长
3.3 months
期刊介绍: BMC Infectious Diseases is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of infectious and sexually transmitted diseases in humans, as well as related molecular genetics, pathophysiology, and epidemiology.
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