Iplikcioglu A Celal, Bek Sirzat, Gokduman Cem A, Cosar Murat, Sav Aydin
Neurosurgery Clinic, Ministry of Health Okmeydani Teaching and Research Hospital, Basibuyuk-Maltepe, Istanbul, Turkey.
Spine (Phila Pa 1976). 2007 Jan 1;32(1):E45-7. doi: 10.1097/01.brs.0000251016.54203.71.
A case report and literature review are presented.
To describe and review the clinical presentations, characteristic findings from imaging studies, types, differential diagnosis, prognosis, and treatment of amyloidoma arising within the vertebrae.
Amyloidoma can occur in the bone, skin, larynx, lymph nodes, urinary bladder, eye, tongue, and gastrointestinal system. However, amyloidomas affecting the vertebral bones are very rare. To our knowledge, only 3 cases of amyloidoma involving cervical spine have been reported previously.
In this report, we present a case of solitary amyloidosis of the cervical spine.
The differential diagnosis of primary solitary spinal amyloidoma includes metastasis, infection, primary bone tumors, plasmocytoma, and Potts abscess. The correct diagnosis can be achieved only after the specific staining of tissue. The prognosis of amyloidosis is related to the specific form of amyloidosis. However, primary solitary amyloidosis has the best prognosis, although a limited number of patients without long-term follow-up studies have been reported.
Primary solitary amyloidosis is a rare form of the amyloidosis, which is different from the other forms of amyloidosis because of excellent prognosis with surgical excision. Combined surgical excision and spinal stabilization is the best treatment.
本文呈现了一例病例报告及文献综述。
描述并综述椎体淀粉样瘤的临床表现、影像学特征、类型、鉴别诊断、预后及治疗。
淀粉样瘤可发生于骨骼、皮肤、喉、淋巴结、膀胱、眼、舌及胃肠道系统。然而,累及椎骨的淀粉样瘤非常罕见。据我们所知,此前仅报道过3例累及颈椎的淀粉样瘤病例。
在本报告中,我们呈现了一例颈椎孤立性淀粉样变性病例。
原发性孤立性脊柱淀粉样瘤的鉴别诊断包括转移瘤、感染、原发性骨肿瘤、浆细胞瘤及寒性脓肿。只有在组织进行特异性染色后才能做出正确诊断。淀粉样变性的预后与淀粉样变性的具体类型有关。然而,原发性孤立性淀粉样变性预后最佳,尽管报道的患者数量有限且缺乏长期随访研究。
原发性孤立性淀粉样变性是淀粉样变性的一种罕见形式,因其手术切除预后良好,与其他形式的淀粉样变性不同。手术切除联合脊柱稳定术是最佳治疗方法。