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酷似化脓性肉芽肿的口腔毛细血管瘤:诊断与治疗的挑战

Oral capillary haemangioma mimicking pyogenic granuloma: a challenge for diagnosis and management.

作者信息

Patil Anil, Pattanshetti Channaveer, Varekar Aniruddha, Huddar Sandhyarani B

机构信息

Department of Pedodontics, Bharati Vidyapeeth Deemed University Dental College and Hospital, Sangli, Maharashtra, India.

出版信息

BMJ Case Rep. 2013 Feb 14;2013:bcr2012007874. doi: 10.1136/bcr-2012-007874.

Abstract

Pyogenic granuloma (PG) is a localised granulation tissue overgrowth, in reaction to mild irritation. The aetiology of the lesion is not known, though it was originally believed to be a botryomycotic infection. The clinical diagnosis of such a lesion can be quite challenging. The purpose of this article is to report an unusual case of benign tumour in an adolescent boy who was clinically diagnosed as PG and histopathologically as capillary haemangioma. PG being a benign lesion; surgical excision was performed and predisposing irritants were removed.

摘要

化脓性肉芽肿(PG)是一种局部肉芽组织过度生长,由轻度刺激引起。尽管最初认为该病变是葡萄球菌性脓皮病感染,但病变的病因尚不清楚。这种病变的临床诊断颇具挑战性。本文旨在报告一例青少年男性的罕见良性肿瘤病例,该病例临床诊断为PG,组织病理学诊断为毛细血管瘤。由于PG是良性病变,故进行了手术切除并去除了诱发刺激因素。

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