伪装成呼吸道乳头状瘤病的喉部淋巴畸形

IF 0.3 Q4 OTORHINOLARYNGOLOGY
B. Kharel, Y. Neupane
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引用次数: 0

摘要

摘要淋巴畸形是头颈部淋巴通道异常的先天性良性病变。广泛的疾病累及喉部并表现为喉部病变是一种罕见的情况,并可能导致诊断上的谜。我们报告一个罕见的病例,广泛的混合囊性型喉淋巴畸形,没有任何外颈部或口腔肿胀,表现为喘鸣,临床模仿青少年呼吸道乳头状瘤病。内镜下减体积和气管造口术,随后的MRI显示淋巴畸形。注射强力霉素硬化治疗失败后,计划明确手术治疗。然而,患者未能随访。淋巴畸形延伸到喉部是一个罕见的气道问题的原因。仅凭病史和临床检查并不总是足以应付每一个病例。在不寻常的情况下,最终的诊断应包括适当的影像学检查,并应由组织病理学证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lymphatic malformation in larynx masquerading as respiratory papillomatosis
Abstract Introduction Lymphatic malformations are benign congenital lesions of abnormal lymphatic channel common in head and neck region. Extensive disease involving the larynx and presenting as a laryngeal pathology is a rare occurrence and can cause diagnostic enigma. Case report We report an unusual case of an extensive mixed cystic type of lymphatic malformation in the larynx without any external neck or oral swelling presenting in stridor and clinically mimicking as juvenile respiratory papillomatosis. Endoscopic debulking and tracheostomy were done and subsequent MRI showed lymphatic malformation. After the failure to inject doxycycline sclerotherapy properly, definite surgery was planned. However, the patient was lost to follow up. Discussion Lymphatic malformation extending into the larynx is a rare cause of airway problem. History and clinical examination alone is not always adequate in every case. In the case of an unusual presentation, the final diagnosis should include appropriate imaging and should be confirmed by histopathology.
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29 weeks
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