Idiopathic avascular necrosis of the scaphoid (Preiser's disease): a case report and review of the literature.

IF 0.4 Q4 SURGERY
Case Reports in Plastic Surgery and Hand Surgery Pub Date : 2024-07-04 eCollection Date: 2024-01-01 DOI:10.1080/23320885.2024.2374550
Jared J Topham, Bret Wehrli, Assaf Kadar
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Abstract

Idiopathic avascular necrosis of the scaphoid bone, Preiser's disease, was originally described as a deteriorative pathology whereby the osseous structure necroses due to loss of blood supply. It may present with multifactorial etiology, which is still largely not well understood. We describe a case of Preiser's disease in a 70-year-old female, with worsening pain and loss of range of motion in her right wrist over a two-year period. Past medical history was significant for Sjogren's disease, fibromyalgia, and dystonia. Pain began several months following traumatic right dorsal wrist injury. Diagnosis of traumatic scaphoid fracture was originally suspected. Conservative treatment was unsuccessful. Radiographs did not demonstrate evidence of primary fracture. CT scan and MRI demonstrated osteonecrosis of the proximal pole of the scaphoid, but no evidence of fracture, either residual or healing, was found. Proximal row carpectomy was performed for avascular necrosis of the scaphoid. Histology confirmed diagnosis and verified absence of fracture. Postoperatively, the patient's pain and range of motion improved. This report combines histological findings of Preiser's disease with radiographic images which may ameliorate understanding of the clinical pathophysiology. We describe an unusual manifestation of Preiser's disease whereby a single traumatic event, in the absence of fracture, led to idiopathic scaphoid avascular necrosis, which may have been associated with Sjogren's syndrome and fibromyalgia. These conditions may have negatively impacted microvasculature and decreased bone mineral density, inversely correlated with the production of fatty marrow, facilitating the onset of osteonecrosis in the scaphoid.

特发性肩胛骨血管性坏死(Preiser 病):病例报告和文献综述。
特发性肩胛骨血管性坏死(Preiser's disease)最初被描述为一种恶化性病变,骨结构因失去血液供应而坏死。它的病因可能是多因素的,但目前人们对这一病因仍不甚了解。我们描述了一例普雷泽氏病病例,患者是一名 70 岁女性,两年来右腕疼痛加剧,活动范围减小。既往病史显示她患有斯约金氏病、纤维肌痛和肌张力障碍。疼痛始于右腕背外伤后数月。最初怀疑是外伤性肩胛骨骨折。保守治疗无效。X光片未显示原发性骨折的证据。CT扫描和核磁共振成像显示肩胛骨近端骨坏死,但未发现骨折迹象,无论是残留骨折还是愈合骨折。为治疗肩胛骨无血管性坏死,患者接受了近端行carpectomy手术。组织学检查确诊并证实没有骨折。术后,患者的疼痛和活动范围均有所改善。本报告结合了普雷泽病的组织学发现和放射影像学图像,有助于加深对临床病理生理学的理解。我们描述了普雷泽病的一种不寻常表现,即在没有骨折的情况下,单一创伤事件导致特发性肩胛骨无血管性坏死,这可能与斯约格伦综合征和纤维肌痛有关。这些病症可能对微血管产生了负面影响,降低了骨矿密度,与脂肪髓的生成成反比,促进了肩胛骨骨坏死的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
40
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