Yamamoto Gaku, Takamura Kei, Ishida Yuriko, Sato Yuma, Sinozaki Ayuka, Kikuchi Hajime, Yamamoto Makoto, Kobayashi Hajime, Hirose Naoki, Kikuchi Keisuke
Department of Respiratory Medicine Obihiro Kosei Hospital Obihiro Japan.
Respirol Case Rep. 2022 Mar 3;10(4):e0924. doi: 10.1002/rcr2.924. eCollection 2022 Apr.
Angioimmunoblastic T-cell lymphoma (AITL) is a type of peripheral T-cell tumour that belongs to the group of non-Hodgkin's lymphomas. Pulmonary lesions can be found in 7%-10% of AITL cases. Imaging findings of the lungs varied; however, immunoblastic infiltration in the lungs is rare. Our patient was a 73-year-old man who received repeated chemotherapy for AITL. Fourth-line therapy using romidepsin controlled the illness, but the patient was hospitalized for dyspnoea and an infiltrative shadow. We performed bronchoalveolar lavage (BAL), and the culture was positive for . The patient was initially discharged with antibiotic therapy, but hospitalized again. Antibiotics were ineffective and the patient required mechanical ventilation. BAL was performed again, after which fluid cytology revealed immunoblast-like atypical cells. Therefore, the patient was diagnosed with pulmonary infiltration due to AITL. Steroid therapy proved ineffective, and the patient died. BAL was used to effectively diagnose pulmonary AITL infiltration.
血管免疫母细胞性T细胞淋巴瘤(AITL)是一种外周T细胞肿瘤,属于非霍奇金淋巴瘤组。7%-10%的AITL病例可出现肺部病变。肺部的影像学表现各异;然而,肺部免疫母细胞浸润罕见。我们的患者是一名73岁男性,因AITL接受了多次化疗。使用罗米地辛的四线治疗控制了病情,但患者因呼吸困难和浸润性阴影住院。我们进行了支气管肺泡灌洗(BAL),培养结果为阳性。患者最初接受抗生素治疗后出院,但再次住院。抗生素治疗无效,患者需要机械通气。再次进行BAL,之后液体细胞学检查发现免疫母细胞样非典型细胞。因此,该患者被诊断为AITL导致的肺部浸润。类固醇治疗无效,患者死亡。BAL被用于有效诊断肺部AITL浸润。