Trauma and Orthopaedics, Royal Devon and Exeter NHS Foundation Trust, Exeter, UK
Trauma and Orthopaedics, Torbay Hospital, Torquay, Torbay, UK.
BMJ Case Rep. 2022 Nov 8;15(11):e251726. doi: 10.1136/bcr-2022-251726.
Osteoclastomas or brown tumours are named as such due to increased vascularity, subsequent haemorrhage and haemosiderin deposition giving the lesion a reddish brown appearance under gross microscopic examination. It is due to an increase in parathyroid hormone activity from several causes, such as parathyroid adenomas, renal impairment and low vitamin D levels. The lesions increase the tendency of the bone to fracture. The challenging aspect of the diagnosis is that a histological diagnosis without immunohistochemistry is impossible to make. This is because, without special staining, brown tumours cannot be differentiated from giant cell tumours, which are also classed as benign but can be locally destructive and has potential for malignant transformation. Once tissue diagnosis is confirmed as a brown tumour, then aggressive forms of treatment are not needed, and they generally resolve once the underlying cause is treated. We describe a woman in her 80s who presented to the local Orthopaedic service with a pathological ankle fracture due to a brown tumour.
破骨细胞瘤或棕色瘤之所以被命名为棕色瘤,是因为其血管增多,随后发生出血和含铁血黄素沉积,使病变在大体显微镜下呈现出红棕色外观。它是由于甲状旁腺激素活性增加所致,原因有多种,如甲状旁腺腺瘤、肾功能不全和维生素 D 水平低。病变增加了骨折的倾向。诊断的挑战性在于,如果没有免疫组织化学,仅凭组织学诊断是不可能的。这是因为,如果没有特殊染色,棕色瘤就无法与同样被归类为良性的巨细胞瘤区分开来,但巨细胞瘤可能具有局部破坏性,并有可能发生恶性转化。一旦组织学诊断为棕色瘤,就不需要进行激进的治疗,一般在治疗根本原因后就会得到解决。我们描述了一位 80 多岁的女性,她因棕色瘤导致病理性踝关节骨折而到当地骨科就诊。