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成人隐匿性T细胞白血病合并肺孢子菌肺炎:1例报告

Smoldering adult T-cell leukemia complicated with pneumocystis pneumonia: A case report.

作者信息

Kawamoto Kazuma, Yamasaki Masahiro, Taniwaki Masaya, Itagaki Mituhiro, Daido Wakako, Matsumoto Yu, Matsumoto Naoko, Izumi Yusuke, Otohara Masaya, Ohashi Nobuyuki, Hattori Noboru

机构信息

Department of Respiratory Medicine, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Naka-ku, Hiroshima, Japan.

Department of Hematology, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Naka-ku, Hiroshima, Japan.

出版信息

Respir Med Case Rep. 2021 Mar 28;33:101404. doi: 10.1016/j.rmcr.2021.101404. eCollection 2021.

Abstract

Adult T-cell leukemia (ATL) is a tumor of CD4-positive T cells that accompanies an infection by human T-cell lymphotropic virus (HTLV-I). ATL is classified into four types-acute, lymphomatous, chronic, and smoldering. Opportunistic infections are known to occur in patients with acute or lymphomatous type ATL; however, whether patients with chronic or smoldering ATL also have a high risk of opportunistic infections is not yet known. Herein, we report a case of pneumocystis pneumonia in a patient with smoldering ATL. He was a 64-year-old man with primary complaints of cough and dyspnea on exertion. A chest radiograph showed infiltration shadows in the left lung field. He was prescribed antibiotics for pneumonia; however, his symptoms worsened, and he developed hypoxemia. White-blood cell count was 13000/μL, and 7% of atypical lymphocytes were found in the smears of peripheral blood cells. His serum β-D glucan concentration was increased to 85.9 pg/mL, and his serum tested positive for anti-HTLV-1 antibody. Chest-computed tomography revealed diffuse ground-glass opacities in the bilateral lung fields. Pneumocystis-polymerase chain reaction performed on bronchoalveolar lavage fluid confirmed pneumocystis, but atypical lymphocytes were not detected via transbronchial lung biopsy. Therefore, he was diagnosed with pneumocystis pneumonia associated with smoldering ATL. Sulfamethoxazole-trimethoprim and corticosteroid therapies were administered to treat the pneumocystis pneumonia, and his symptoms and lung shadows improved rapidly. Thus, opportunistic infections, including pneumocystis pneumonia, may be caused by smoldering ATL. In the case of atypical lymphocyte detection in peripheral-blood smears, clinicians should consider the possibility of ATL.

摘要

成人T细胞白血病(ATL)是一种CD4阳性T细胞肿瘤,伴有人类嗜T淋巴细胞病毒(HTLV-I)感染。ATL分为四种类型——急性、淋巴瘤型、慢性和潜伏型。已知急性或淋巴瘤型ATL患者会发生机会性感染;然而,慢性或潜伏型ATL患者是否也有较高的机会性感染风险尚不清楚。在此,我们报告一例潜伏型ATL患者发生肺孢子菌肺炎的病例。他是一名64岁男性,主要症状为咳嗽和劳力性呼吸困难。胸部X线片显示左肺野有浸润阴影。他因肺炎接受了抗生素治疗;然而,他的症状恶化,出现了低氧血症。白细胞计数为13000/μL,外周血细胞涂片发现7%的非典型淋巴细胞。他的血清β-D葡聚糖浓度升至85.9 pg/mL,血清抗HTLV-1抗体检测呈阳性。胸部计算机断层扫描显示双侧肺野弥漫性磨玻璃影。对支气管肺泡灌洗 fluid进行的肺孢子菌聚合酶链反应证实了肺孢子菌,但经支气管肺活检未检测到非典型淋巴细胞。因此,他被诊断为与潜伏型ATL相关的肺孢子菌肺炎。给予磺胺甲恶唑-甲氧苄啶和皮质类固醇疗法治疗肺孢子菌肺炎,他的症状和肺部阴影迅速改善。因此,包括肺孢子菌肺炎在内的机会性感染可能由潜伏型ATL引起。在外周血涂片检测到非典型淋巴细胞的情况下,临床医生应考虑ATL的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53f8/8348172/796adadcc4e9/gr1.jpg

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