Giant Cell Lesions of the Jaws: A Work on Current Concepts and Making Through a Working Classification.

IF 3.2 Q2 PATHOLOGY Head & Neck Pathology Pub Date : 2024-09-16 DOI:10.1007/s12105-024-01655-0
Ayushi Jain, Arushi Tomar, Sharon John, Shalini Gupta
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Abstract

Introduction: Giant cell-rich lesions are a diverse group of lesions that usually occur in bone and contain varying numbers of reactive osteoclastic-type multinucleate giant cells. These lesions present a challenge in pathologic diagnosis, often requiring a combination of clinical, radiographic, and histopathological assessments. The present retrospective observational study aims to provide a concise diagnostic criterion by combining all these parameters, which will aid in effective diagnosis and targeted treatment planning in the future.

Material and method: Previously diagnosed cases of these lesions were taken from the archives and categorized as Central Giant Cell Granuloma (CGCG), CGCG with secondary Aneurysmal Bone Cyst (ABC), primary ABC, and Brown's Tumour. Their demographic characteristics along with clinical, radiological, and histological data were retrieved and compiled into the table. The data was then analyzed and classified into aggressive and non-aggressive CGCG according to the criteria set in the study.

Result: 10 reported cases were of isolated CGCG, 5 were CGCG with secondary ABC, 5 of Brown's tumor and 3 were that of conventional ABC. Out of these, the lesions showing extensive size along with an increased number of giant cells were categorized under aggressive CGCG, whereas those with less aggressive characteristics were categorized under non-aggressive CGCG. The aggressive category comprised 5 cases of isolated CGCG, 2 cases of CGCG with secondary ABC, 3 cases of primary ABC, and 5 of brown tumor, whilst the rest of the cases were categorized under non-aggressive CGCG.

Conclusion: Since all these share overlapping features, thereby this type of concise categorization is the dire need so that the lesions can have a precise diagnosis with treatment and follow-up intervals for aggressive lesions.

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颚部巨细胞病变:关于当前概念和工作分类的研究》(Giant Cell Lesions of the Jaws: A Work on Current Concepts and Making Through a Working Classification.
导言:富含巨细胞的病变是一类多种多样的病变,通常发生在骨骼中,含有不同数量的反应性破骨细胞型多核巨细胞。这些病变给病理诊断带来了挑战,通常需要结合临床、放射学和组织病理学评估。本回顾性观察研究旨在结合所有这些参数,提供一个简明的诊断标准,这将有助于今后的有效诊断和有针对性的治疗计划:这些病变的既往诊断病例均来自档案,分为中央巨细胞肉芽肿(CGCG)、中央巨细胞肉芽肿伴继发性动脉瘤性骨囊肿(ABC)、原发性ABC和布朗瘤。他们的人口统计学特征以及临床、放射学和组织学数据均被检索出来并编制成表格。结果:报告的病例中,10 例为孤立性 CGCG,5 例为伴有继发性 ABC 的 CGCG,5 例为布朗瘤,3 例为传统 ABC。在这些病例中,病变面积较大、巨细胞数量增多的病例被归类为侵袭性 CGCG,而侵袭性较低的病例被归类为非侵袭性 CGCG。侵袭性类别包括 5 例孤立的 CGCG、2 例伴有继发性 ABC 的 CGCG、3 例原发性 ABC 和 5 例棕色肿瘤,而其余病例则被归类为非侵袭性 CGCG:结论:由于所有这些肿瘤都有重叠的特征,因此迫切需要这种简明的分类方法,以便对病变进行精确诊断,并对侵袭性病变进行治疗和随访。
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来源期刊
CiteScore
5.70
自引率
9.50%
发文量
99
期刊介绍: Head & Neck Pathology presents scholarly papers, reviews and symposia that cover the spectrum of human surgical pathology within the anatomic zones of the oral cavity, sinonasal tract, larynx, hypopharynx, salivary gland, ear and temporal bone, and neck. The journal publishes rapid developments in new diagnostic criteria, intraoperative consultation, immunohistochemical studies, molecular techniques, genetic analyses, diagnostic aids, experimental pathology, cytology, radiographic imaging, and application of uniform terminology to allow practitioners to continue to maintain and expand their knowledge in the subspecialty of head and neck pathology. Coverage of practical application to daily clinical practice is supported with proceedings and symposia from international societies and academies devoted to this field. Single-blind peer review The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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