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滑膜炎、痤疮、脓疱病、骨肥厚、骨炎综合征(SAPHO)的骨表现。

Osseous manifestations of SAPHO (synovitis, acne, pustulosis, hyperostosis, osteitis) syndrome.

作者信息

Reith J D, Bauer T W, Schils J P

机构信息

Department of Anatomic Pathology, Cleveland Clinic Foundation, OH 44195, USA.

出版信息

Am J Surg Pathol. 1996 Nov;20(11):1368-77. doi: 10.1097/00000478-199611000-00008.

Abstract

The SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome includes a complex group of disorders characterized by peculiar bone lesions, most commonly involving the anterior chest wall, and sometimes accompanied by dermatologic manifestations. The clinical and radiographic features of this syndrome are well described, but few studies have examined the histologic features of the bone lesions. We describe the clinical, radiographic, and histologic features of the osseous lesions encountered in eight patients with a clinical diagnosis of SAPHO syndrome. The patients included five female and three male patients ranging in age from 5 to 63 years (mean, 35.3 years). The most common clinical presentation was pain related to the sites of osseous involvement. Two patients also had some form of pustular dermatosis. The radiographic features of the osseous lesions varied but often suggested the possibility of a neoplasm. Nine pathologic specimens were available for review, five from the clavicle, two from the first rib, one from the calcaneus/cuboid, and one from the tibia. The histologic features varied but seemed related to the duration of the patients' musculoskeletal symptoms. Early lesions contained acute inflammation, edema, and prominent periosteal bone formation, histologically indistinguishable from ordinary bacterial osteomyelitis, whereas late lesions demonstrated markedly sclerotic bone trabeculae with prominent marrow fibrosis and only mild chronic inflammation; one of these biopsies appeared virtually identical to Paget's disease. One biopsy was performed after an intermediate duration of symptoms and contained prominent chronic inflammation only. The histologic findings in SAPHO are variable and nonspecific and may depend on the duration of disease, but it is important to recognize the spectrum of histologic changes possible in the syndrome and to realize that clinicopathologic correlation is necessary to avoid misdiagnosis and unnecessary long-term antibiotic therapy.

摘要

SAPHO(滑膜炎、痤疮、脓疱病、骨质增生和骨炎)综合征包括一组复杂的疾病,其特征为特殊的骨病变,最常累及前胸壁,有时伴有皮肤表现。该综合征的临床和影像学特征已有充分描述,但很少有研究探讨骨病变的组织学特征。我们描述了8例临床诊断为SAPHO综合征患者骨病变的临床、影像学和组织学特征。患者包括5名女性和3名男性,年龄从5岁至63岁不等(平均35.3岁)。最常见的临床表现是与骨受累部位相关的疼痛。2例患者还患有某种形式的脓疱性皮肤病。骨病变的影像学特征各不相同,但常提示有肿瘤的可能。有9份病理标本可供检查,5份来自锁骨,2份来自第一肋骨,1份来自跟骨/骰骨,1份来自胫骨。组织学特征各不相同,但似乎与患者肌肉骨骼症状的持续时间有关。早期病变含有急性炎症、水肿和明显的骨膜骨形成,组织学上与普通细菌性骨髓炎无法区分,而晚期病变则显示出明显硬化的骨小梁,伴有明显的骨髓纤维化和仅轻度的慢性炎症;其中一份活检标本的表现与佩吉特病几乎相同。一份活检标本是在症状持续时间处于中间阶段时进行的,仅含有明显的慢性炎症。SAPHO的组织学表现多样且无特异性,可能取决于疾病的持续时间,但重要的是要认识到该综合征可能出现的组织学变化范围,并意识到临床病理相关性对于避免误诊和不必要的长期抗生素治疗是必要的。

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