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腮腺腺样囊性癌脊柱转移:两例报告。

Metastasis of spine from adenoid cystic carcinoma of the parotid gland: two case reports.

机构信息

Knee and Sport Medicine Research Center, Milad General Hospital, Tehran, Iran.

Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Arabi Ave, Daneshjoo Blvd, Velenjak, Tehran, 19839-63113, Iran.

出版信息

J Med Case Rep. 2023 May 15;17(1):196. doi: 10.1186/s13256-023-03926-w.

DOI:10.1186/s13256-023-03926-w
PMID:37183252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10184352/
Abstract

BACKGROUND

Spinal metastasis from adenoid cystic carcinoma of the salivary gland is extremely rare. We present two interesting cases of spinal metastasis from adenoid cystic carcinoma of the parotid gland. A 29-year-old Persian male and a 48-year-old Persian female presented with parotid gland mass. The two patients received parotidectomy and radiotherapy. The pathological examination result was adenoid cystic carcinoma. Because of intractable back pain, patients were referred to the hospital after 7 years and 9 months, respectively. Both cases underwent spinal surgery. Histopathology confirmed spinal metastasis from adenoid cystic carcinoma of the parotid gland (case 1: T6, T12, and L1; case 2: T12). Anterior corpectomy of T12 and lateral screw fixation at T11 and L1 were done in case 2. Posterior spinal fusions from T2 to L3 and from T10 to L2 were performed in case 1 and case 2, respectively. Both patients showed good clinical improvement. The last follow-up (case 1: 24 months; case 2: 6 months after surgery), plain radiographs and computed tomography scan showed good fusion without instrumental failure and magnetic resonance imaging revealed good decompression of the spinal cord of both cases.

CONCLUSION

Although spinal metastasis from adenoid cystic carcinoma of the parotid gland is extremely rare, it is necessary to be careful in the differential diagnosis.

摘要

背景

来自涎腺腺样囊性癌的脊柱转移极为罕见。我们报告两例来自腮腺的腺样囊性癌脊柱转移的有趣病例。一名 29 岁的波斯男性和一名 48 岁的波斯女性因腮腺肿块就诊。两名患者均接受了腮腺切除术和放疗。病理检查结果为腺样囊性癌。由于难治性背痛,两名患者分别在 7 年后和 9 个月后转诊至医院。两名患者均接受了脊柱手术。组织病理学证实为来自腮腺的腺样囊性癌脊柱转移(病例 1:T6、T12 和 L1;病例 2:T12)。病例 2 行 T12 前路椎体切除术和 T11、L1 侧方螺钉固定。病例 1 和病例 2 分别行 T2 至 L3 和 T10 至 L2 的后路脊柱融合术。两名患者的临床症状均得到显著改善。末次随访(病例 1:24 个月;病例 2:术后 6 个月)时,X 线平片和 CT 扫描显示融合良好,无器械失败,磁共振成像显示脊髓减压效果良好。

结论

虽然来自腮腺的腺样囊性癌的脊柱转移极为罕见,但在鉴别诊断时仍需小心谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe9/10184352/dcb377d9f030/13256_2023_3926_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe9/10184352/c3391e739122/13256_2023_3926_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe9/10184352/dcb377d9f030/13256_2023_3926_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe9/10184352/c3391e739122/13256_2023_3926_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fe9/10184352/dcb377d9f030/13256_2023_3926_Fig2_HTML.jpg

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