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扁桃体错构瘤性息肉:一例报告

Hamartomatous polyp of the tonsil: A case report.

作者信息

Singh M, Mundi D K, Kaur I, Kaur A

机构信息

Department of ENT, Government Medical College and Rajindra Hospital, Patiala, Punjab, India.

Department of General Surgery, Government Medical College and Rajindra Hospital, Patiala, Punjab, India.

出版信息

Niger J Clin Pract. 2017 Jun;20(6):774-776. doi: 10.4103/njcp.njcp_338_16.

Abstract

Hamartomatous polyps of the tonsil are rare. They have been described using various terms such as a lymphangiomatous polyp, lymphangiectatic fibrous polyp, lipomatous polyp, or pedunculated tonsil; hence, the actual incidence is difficult to be quantified. Polyp of the palatine tonsils is an unusual benign lesion of the head and neck. It is a rare polypoidal mass that generally arises from a pedicle attached to the tonsil and projecting into the oropharynx. Polypoid lesions of the head and neck are likewise rare, and such tumors arising from the palatine tonsils are sparse. Tonsillar polyp is an uncommon hamartomatous lesion that generally arises from the tonsillar surface. It has rarely been reported in the medical literature. We present a case of hamartomatous polyp of the palatine tonsil in a 17-year-old male patient.

摘要

扁桃体错构瘤性息肉较为罕见。它们曾被用各种术语描述,如淋巴管瘤性息肉、淋巴管扩张性纤维息肉、脂肪瘤性息肉或带蒂扁桃体;因此,实际发病率难以量化。腭扁桃体息肉是头颈部一种不常见的良性病变。它是一种罕见的息肉样肿物,通常起自附着于扁桃体并突入口咽的蒂部。头颈部的息肉样病变同样罕见,而起源于腭扁桃体的此类肿瘤更是稀少。扁桃体息肉是一种不常见的错构瘤性病变,通常起自扁桃体表面。医学文献中对此报道很少。我们报告一例17岁男性患者的腭扁桃体错构瘤性息肉病例。

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