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颌骨多灶性溶骨性病变作为甲状旁腺功能亢进棕色瘤诊断的路线图:1例罕见病例报告并文献复习

Multifocal osteolytic lesions of jaw as a road map to diagnosis of brown tumor of hyperparathyroidism: A rare case report with review of literature.

作者信息

Gosavi Suchitra, Kaur Harpreet, Gandhi Pramod

机构信息

Department of Oral Pathology, Government Dental College and Hospital, Nagpur, Maharashtra, India.

Division of Oral Pathology, Centre of Dental Education and Research, All India Institute of Medical Sciences, New Delhi, India.

出版信息

J Oral Maxillofac Pathol. 2020 Feb;24(Suppl 1):S59-S66. doi: 10.4103/jomfp.JOMFP_319_19. Epub 2020 Feb 28.

DOI:10.4103/jomfp.JOMFP_319_19
PMID:32189907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7069142/
Abstract

Brown tumor is unifocal or multifocal bone disease which represents terminal stage of hyperparathyroidism (HPT)-dependent bone pathology. It is recognized as a component of metabolic bone disease called osteitis fibrosa cystica generalisata or Von Recklinghausen disease of bone. HPT was first described by Von Recklinghausen in 1891. Brown tumor diagnosis nowadays is less frequently encountered because of early stage detection of HPT. This early detection is possible due to routine blood screening in asymptomatic adults or during evaluation of osteoporosis. Histologically, it may resemble any other giant cell lesion of the jaw that imposes diagnostic challenge and delay in treatment. We are introducing a case report of a 30-year-old female patient presented with multifocal osteolytic lesions in mandible with histopathology depictive of giant cell granuloma. Further biochemical investigations and X-ray skeletal changes raised the suspicion of primary HPT which was confirmed by parathyroid scintigraphy revealing parathyroid adenoma. The main purpose of this case report is to reinforce the role of oral examination in diagnosis of systemic diseases and to propose a diagnostic layout/algorithm when giant cells are present in biopsy specimen. Review of literature showing brown tumor of oral cavity associated with PHPT is discussed.

摘要

棕色瘤是一种单灶性或多灶性骨疾病,代表甲状旁腺功能亢进症(HPT)相关骨病变的终末期。它被认为是一种代谢性骨病的组成部分,称为全身性纤维囊性骨炎或骨的冯·雷克林豪森病。HPT最早由冯·雷克林豪森于1891年描述。由于HPT的早期检测,如今棕色瘤的诊断较少见。由于对无症状成年人进行常规血液筛查或在评估骨质疏松症期间进行检查,这种早期检测成为可能。在组织学上,它可能类似于颌骨的任何其他巨细胞病变,这给诊断带来挑战并导致治疗延迟。我们介绍一例30岁女性患者的病例报告,该患者下颌骨出现多灶性溶骨性病变,组织病理学表现为巨细胞肉芽肿。进一步的生化检查和X线骨骼改变引发了原发性HPT的怀疑,甲状旁腺闪烁显像显示甲状旁腺腺瘤证实了这一诊断。本病例报告的主要目的是强化口腔检查在全身性疾病诊断中的作用,并在活检标本中存在巨细胞时提出一种诊断布局/算法。讨论了显示口腔棕色瘤与原发性甲状旁腺功能亢进症相关的文献综述。

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