A case of pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma in a patient with a history of idiopathic lymphocytic interstitial pneumonia (iLIP).

Katsushi Toyohara, Hiroya Ishihara, Takuro Morita, Yuki Shindo, Sho Takeda, Satoshi Fumimoto, Kaoru Ochi, Yoshio Ichihashi, Kiyoshi Sato, Hiroko Kuwabara, Nobuharu Hanaoka, Takahiro Katsumata
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Abstract

Background: Pulmonary mucosa-associated lymphoid tissue (MALT) lymphoma and idiopathic lymphocytic interstitial pneumonia (iLIP) are rare pulmonary diseases. MALT lymphoma is an extranodal marginal zone lymphoma (EMZL), whereas LIP is a benign lymphoproliferative disorder characterized by lymphocytic infiltration of the lungs. LIP should be closely monitored, as it has the potential to undergo malignant transformation into MALT lymphoma.

Case presentation: A 45-year-old woman was diagnosed with LIP and followed up for 9 years before being referred to our hospital due to an enlarging shadow on chest radiographs. The volume of the sample collected via bronchoscopy was too small to make a diagnosis, so the patient underwent surgery. The pathology results revealed diffuse proliferation of medium-sized lymphocytes filling the alveolar spaces, leading to a diagnosis of MALT lymphoma. After a thorough examination, no other lesions were found, confirming the diagnosis of EMZL of the lung, a primary pulmonary lymphoma (PPL). No postoperative treatment was administered after surgery; however, 2 years later, recurrence was detected in the stomach, and the patient underwent chemotherapy. Complete remission was achieved through chemotherapy, and the patient has been recurrence-free for 3 years since her treatment.

Conclusions: We report a rare case of MALT lymphoma that developed 9 years after the diagnosis of LIP. Since LIP can undergo malignant transformation into EMZL, it is important to be aware of this possibility. Differentiating between the two diseases onthe basis ofclinical and imaging findings is challenging, so biopsytechniques, such as transbronchial biopsy, CT-guided needle aspiration biopsy, and surgical resection, are essential. While surgery is the standard treatment for primary pulmonary lymphoma, observation is a viable option, as it provides results comparable to those of other treatment approaches.

有特发性淋巴细胞间质性肺炎(iLIP)病史的患者发生肺粘膜相关淋巴组织(MALT)淋巴瘤病例。
背景:肺粘膜相关淋巴组织(MALT)淋巴瘤和特发性淋巴细胞间质性肺炎(iLIP)是罕见的肺部疾病。MALT淋巴瘤是一种结外边缘区淋巴瘤(EMZL),而LIP是一种以肺淋巴细胞浸润为特征的良性淋巴增生性疾病。LIP应密切监测,因为它有可能发生恶性转化为MALT淋巴瘤。病例介绍:一名45岁女性被诊断为唇腭裂,随访9年后因胸片阴影增大而转诊至我院。通过支气管镜检查收集的样本体积太小,无法进行诊断,因此患者接受了手术。病理结果显示弥漫增生的中等大小淋巴细胞充满肺泡间隙,导致MALT淋巴瘤的诊断。经彻底检查,未发现其他病变,确认诊断为肺EMZL,原发性肺淋巴瘤(PPL)。术后未进行任何治疗;然而,2年后,发现胃复发,患者接受了化疗。通过化疗完全缓解,患者治疗后3年无复发。结论:我们报告一例罕见的MALT淋巴瘤,在诊断为LIP后9年发生。由于LIP可以恶性转化为EMZL,因此意识到这种可能性是很重要的。根据临床和影像学表现来区分两种疾病是具有挑战性的,因此生物技术,如经支气管活检、ct引导下的穿刺活检和手术切除是必不可少的。虽然手术是原发性肺淋巴瘤的标准治疗方法,但观察是一种可行的选择,因为它提供的结果与其他治疗方法相当。
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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