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首页> 外文期刊>Sao Paulo Medical Journal >Mucosa-associated lymphoid tissue lymphoma of the trachea: case report
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Mucosa-associated lymphoid tissue lymphoma of the trachea: case report

机译:气管粘膜相关淋巴样组织淋巴瘤:病例报告

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CONTEXT: Mucosa-associated lymphoid tissue (MALT) lymphomas are most commonly found in the stomach, lungs, orbital soft tissue, salivary glands and thyroid. Involvement of the trachea is extremely rare. CASE REPORT: This report describes a rare case of MALT lymphoma of the trachea in a 71-year-old woman who presented with a one-year history of coughing, dyspnea, hoarseness and weight loss. There was an infiltrative lesion in the mid-trachea. The anatomopathological diagnosis was only made from the fifth endoscopic biopsy attempt. Immunochemotherapy consisting of rituximab, cyclophosphamide, vincristine and prednisone (R-COP) induced complete remission of the symptoms and endoscopic lesion. CONCLUSIONS: MALT lymphoma of the trachea is extremely rare and indolent disease. It has to be considered in the differential diagnosis of airway lesions. It is crucial to obtain an anatomopathological diagnosis from a specialized pathologist. Immunochemotherapy with R-COP induced complete remission of the disease.
机译:背景:粘膜相关淋巴组织(MALT)淋巴瘤最常见于胃,肺,眼眶软组织,唾液腺和甲状腺。气管受累极少见。病例报告:该报告描述了一位71岁女性的罕见气管MALT淋巴瘤病例,该女性患有咳嗽,呼吸困难,声音嘶哑和体重减轻的病史为一年。气管中部有浸润性病变。解剖病理学诊断仅由第五次内镜活检尝试做出。由利妥昔单抗,环磷酰胺,长春新碱和泼尼松(R-COP)组成的免疫化学疗法可完全缓解症状和内镜病变。结论:气管MALT淋巴瘤是极为罕见的惰性疾病。在气道病变的鉴别诊断中必须考虑到这一点。从专门的病理学家那里获得解剖病理学诊断至关重要。 R-COP免疫化学疗法可完全缓解该病。

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