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丛状成釉细胞瘤的诊断难点。

Difficulties in the diagnosis of plexiform ameloblastoma.

作者信息

Castro-Silva Igor Iuco, Israel Monica Simoes, Lima Glauco Siqueira, de Queiroz Chaves Lourenço Simone

机构信息

Faculty of Dentistry, Salgado de Oliveira University (UNIVERSO), Niteroi, RJ, Brazil.

出版信息

Oral Maxillofac Surg. 2012 Mar;16(1):115-8. doi: 10.1007/s10006-011-0265-x. Epub 2011 Mar 1.

Abstract

BACKGROUND

Plexiform ameloblastoma is a rare and benign odontogenic tumor which may reach grotesque proportions affecting over a region of lower molars. The correct diagnosis is essential to reduce this risk of local recurrences and obtain an effective treatment.

CASE REPORT

A 10-year-old female patient, Caucasian, presented a complaint of painless facial asymmetry. The clinical and imaginological examinations showed an increase in volume in the left mandibular body related to radiolucent unilocular injury near the apex of the first molar, expansion of the vestibular cortical bone, and tooth root resorption ipsilaterally. The former intraosseous biopsy suggested an aneurysmal bone cyst. In reopening the previous marsupialization, a new biopsy was performed with histopathologic findings compatible with plexiform ameloblastoma associated with acute inflammation. Curettage was performed in the region associated with cryotherapy. At the last biopsy, the diagnosis of plexiform ameloblastoma was confirmed with multiple cystic formations and areas of foreign body reaction. The patient is being followed for 2 years and yet remains clinically and radiographically stable with no recurrence.

DISCUSSION

This case reports the importance of selecting the correct area of biopsy of an intraosseous extended lesion to contribute to the diagnosis and treatment of plexiform ameloblastoma.

摘要

背景

丛状成釉细胞瘤是一种罕见的良性牙源性肿瘤,可长得奇形怪状,累及下颌磨牙区。正确诊断对于降低局部复发风险并获得有效治疗至关重要。

病例报告

一名10岁白种女性患者,主诉无痛性面部不对称。临床和影像学检查显示左下颌体体积增大,与第一磨牙根尖附近的透射性单房性损害有关,前庭皮质骨扩张,同侧牙根吸收。先前的骨内活检提示为动脉瘤性骨囊肿。在重新打开之前的袋形缝合术时,进行了新的活检,组织病理学结果与伴有急性炎症的丛状成釉细胞瘤相符。在与冷冻治疗相关的区域进行了刮除术。在最后一次活检时,通过多个囊性结构和异物反应区域确诊为丛状成釉细胞瘤。该患者已随访2年,临床和影像学上仍保持稳定,无复发。

讨论

本病例报告了选择骨内扩展性病变正确活检区域对丛状成釉细胞瘤诊断和治疗的重要性。

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