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A Rare Case of Primary Pulmonary Anaplastic Large Cell Lymphoma

机译:原发性肺间变性大细胞淋巴瘤罕见病例。

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摘要

Non-Hodgkin lymphomas are rare causes of primary lung neoplasms and most are B-cell in origin. Anaplastic large cell lymphoma is an exceedingly rare type of primary pulmonary lymphoma, with an aggressive clinical course.We present the case of an 85-year old male patient who attended our Emergency Department complaining of respiratory and constitutional symptoms, and who was found to have a bronchial mass causing subtotal atelectasis of the left lung. Histological examination showed an anaplastic large cell lymphoma and further investigation revealed that it was limited to the lung. To our knowledge, very few similar cases have been reported in the literature.LEARNING POINTS class="unordered" style="list-style-type:disc">Non-Hodgkin lymphomas are rare causes of pulmonary lung neoplasms, with the majority of cases being marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue or diffuse large B-cell lymphoma.Anaplastic large cell lymphoma (ALCL) usually involves the lymph nodes, skin and soft tissue. It follows an aggressive clinical course and constitutional symptoms are frequent at presentation. Lung involvement may occur as a result of dissemination in up to 12% of cases. Primary ALCL of the lung is extremely rare.Anaplastic lymphoma kinase (ALK) expression is an important prognostic factor, with ALK+ ALCL patients experiencing better outcomes. Adverse prognostic factors also include advanced age, serum lactate dehydrogenase levels and early relapse after therapy. class="kwd-title">Keywords: Anaplastic large cell lymphoma, ALK positive, primary lung lymphoma, lung neoplasm class="head no_bottom_margin" id="idm139708180403824title">INTRODUCTIONNon-Hodgkin lymphoma arising in the lung is rare, accounting for only 0.3% of primary lung neoplasms[–]. Marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) and diffuse large B-cell lymphoma are responsible for 95% of all primary pulmonary lymphomas[–]. Primary anaplastic large cell lymphoma (ALCL) of the lung is an extremely rare type of lung malignancy[].We report a case of primary pulmonary ALCL presenting with a rapidly growing bronchial mass in an 85-year-old man.
机译:非霍奇金淋巴瘤是原发性肺肿瘤的罕见病因,且大多数起源于B细胞。间变性大细胞淋巴瘤是一种极为罕见的原发性肺淋巴瘤,具有侵袭性的临床病程。我们报道了一名85岁的男性患者,该患者就诊于急诊科,主诉呼吸道和体质症状,并被发现患有引起左肺亚肺不张的支气管肿块。组织学检查显示间变性大细胞淋巴瘤,进一步研究表明它仅限于肺。据我们所知,文献中几乎没有类似案例的报道。学习要点 class =“ unordered” style =“ list-style-type:disc”> <!-list-behavior = unordered prefix-word = mark -type = disc max-label-size = 0-> li>非霍奇金淋巴瘤是肺部肺肿瘤的罕见病因,多数病例是粘膜相关淋巴组织的边缘区B细胞淋巴瘤或弥漫性大B细胞淋巴瘤。 间变性大细胞淋巴瘤(ALCL)通常涉及淋巴结,皮肤和软组织。它遵循侵略性的临床过程,并且在出现时经常出现体质症状。在多达12%的病例中,扩散可能会导致肺部受累。肺原发性ALCL极为罕见。 间变性淋巴瘤激酶(ALK)表达是重要的预后因素,ALK + ALCL患者的预后较好。不良预后因素还包括高龄,血清乳酸脱氢酶水平和治疗后早期复发。 class =“ kwd-title”>关键字:间变性大细胞淋巴瘤,ALK阳性,原发性肺淋巴瘤,肺肿瘤 class =“ head no_bottom_margin” id =“ idm139708180403824title”>引言在肺部发生的非霍奇金淋巴瘤罕见,仅占原发性肺肿瘤的0.3% [– ] 。粘膜相关淋巴样组织(MALT)的边缘区B细胞淋巴瘤和弥漫性大B细胞淋巴瘤占所有原发性肺淋巴瘤的95% [–] 。肺原发性间变性大细胞淋巴瘤(ALCL)是一种极为罕见的肺恶性肿瘤。 [] 。我们报道了一例原发性肺ALCL病例,该病在85岁时呈快速增长的支气管肿块。老人

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