Pneumocystis jirovecii Pneumonia: Typical and Atypical CT Findings in a Large Cohort of Immunocompromised Patients with and without HIV.

IF 4.2 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Aaron M Pulsipher, Kealy Ham, Holenarasipur R Vikram, Kyle J Henry, Emily R Thompson, Michael B Gotway
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Abstract

Pneumocystis jirovecii, an atypical fungus, is a recognized cause of severe pneumonia in individuals with HIV. However, P jirovecii pneumonia (PJP) is now increasingly encountered among immunocompromised patients without HIV, including those receiving treatment for hematologic or solid organ malignancies, solid organ or bone marrow transplant recipients, patients with autoimmune diseases treated with immunosuppressive therapy, and patients requiring prolonged corticosteroid therapy; many of whom may not receive prophylaxis. This article summarizes characteristic and atypical chest CT findings of PJP in immunocompromised patients to support early recognition. Diffuse pulmonary ground-glass opacity (GGO) is the most common chest CT manifestation and should strongly suggest PJP in immunocompromised patients, although variant patterns, particularly peripheral and upper lobe predominant distributions, are frequently observed; midlung and basilar distributions are rare. Consolidation is also common, especially in more severely ill patients, but neither GGO nor consolidation distribution reliably differs across underlying causes of immunocompromise. Interlobular septal thickening and mosaic attenuation are additional CT findings, and, although lymphadenopathy and pleural effusion may occur, these often reflect the underlying condition causing immunocompromise or comorbid disease rather than PJP itself. Cyst formation may be observed and can predispose to pneumothorax. CT abnormalities often improve quickly after initiation of PJP-directed therapy, but not in all patients. Atypical CT manifestations, including nodules (with solid nodules potentially representing "granulomatous" PJP), masses, and cavitation, should raise suspicion for coinfection or other superimposed processes. Complex or mixed CT patterns in patients with PJP may result from the disease predisposing to immunocompromise or from its treatment, underscoring the importance of clinical context in interpreting chest CT findings. Keywords: CT, Pulmonary, Thorax, Lung, Infection, Transplantation, Pneumocystis jirovecii Pneumonia, Immunosuppression, Ground-Glass Opacity Supplemental material is available for this article. © RSNA, 2026.

吉氏肺囊虫肺炎:一大群有和没有HIV的免疫功能低下患者的典型和非典型CT表现。
吉氏肺囊虫是一种非典型真菌,是艾滋病毒感染者严重肺炎的公认病因。然而,帕罗维奇肺炎(PJP)现在越来越多地出现在没有HIV的免疫功能低下患者中,包括接受血液或实体器官恶性肿瘤治疗的患者,实体器官或骨髓移植接受者,接受免疫抑制治疗的自身免疫性疾病患者,以及需要长期皮质类固醇治疗的患者;他们中的许多人可能没有得到预防。本文总结了免疫功能低下患者PJP的特征性和非典型胸部CT表现,以支持早期识别。弥漫性肺磨玻璃影(GGO)是最常见的胸部CT表现,在免疫功能低下的患者中强烈提示PJP,尽管经常观察到不同的模式,特别是外周和上肺叶为主的分布;肺中及基底分布少见。实变也很常见,特别是在病情较重的患者中,但GGO和实变分布在免疫功能低下的潜在原因之间都没有可靠的差异。小叶间隔增厚和马赛克衰减是附加的CT表现,尽管可能出现淋巴结病变和胸腔积液,但这些通常反映的是导致免疫功能低下或共病的潜在疾病,而不是PJP本身。可观察到囊肿形成,并可诱发气胸。CT异常通常在pjp定向治疗开始后迅速改善,但并非所有患者都如此。不典型的CT表现包括结节(实性结节可能代表肉芽肿性PJP)、肿块和空化,应怀疑合并感染或其他叠加性病变。PJP患者的复杂或混合CT表现可能是由于该疾病易导致免疫功能低下或治疗所致,这强调了临床背景在解释胸部CT表现时的重要性。关键词:CT,肺,胸,肺,感染,移植,乙氏肺囊虫肺炎,免疫抑制,毛玻璃混浊。©rsna, 2026。
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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