Primary tracheal lymphoma with thyroid carcinoma

IF 0.3 Q4 OTORHINOLARYNGOLOGY
Yuki Irifune, Takashi Mukaigawa, M. Fukaya, Yuko Kakuda, N. Hato
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引用次数: 0

Abstract

Abstract Malignant lymphoma (ML) and papillary thyroid carcinoma (PTC) are the most common hematological and endocrine malignancies. However, ML originating from the intratracheal region is rare, with few reported cases in the literature. We report a case of a 57-year-old woman with double primary cancer, consisting of ML of the intratracheal region and PTC in the isthmus. She complained of hoarseness and exertional dyspnea. Adjacent tumors through the anterior tracheal wall were initially considered as tracheal invasion of the thyroid carcinoma. However, MRI and PET-CT suggested that these tumors had different radiological signs. We performed thyroidectomy and biopsy of the intratracheal tumor with a tracheostomy. Pathological examination revealed PTC and CD-5-positive B-cell indolent intratracheal lymphoma. She received weekly infusions of rituximab for eight weeks after surgery. The intratracheal ML showed complete response, and the tracheocutaneous fistula was closed six months after the initial surgery.
原发性气管淋巴瘤合并甲状腺癌
恶性淋巴瘤(ML)和甲状腺乳头状癌(PTC)是最常见的血液和内分泌恶性肿瘤。然而,起源于气管内区域的ML是罕见的,文献中很少报道病例。我们报告一例57岁女性双原发癌,包括气管内ML和峡部PTC。她抱怨声音嘶哑和用力呼吸困难。通过气管前壁的邻近肿瘤最初被认为是气管侵犯甲状腺癌。然而,MRI和PET-CT显示这些肿瘤具有不同的放射学征象。我们行甲状腺切除术和气管内肿瘤活检,并行气管切开术。病理检查显示PTC和cd -5阳性b细胞惰性气管内淋巴瘤。术后8周,患者每周接受利妥昔单抗输注。气管内ML完全缓解,初次手术后6个月气管皮瘘闭合。
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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9
审稿时长
29 weeks
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