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头颈部髓外浆细胞瘤

Extramedullary plasmacytomas of the head and neck.

作者信息

Wax M K, Yun K J, Omar R A

机构信息

Department of Otolaryngology-Head and Neck Surgery, University, Morgantown 26506-9200.

出版信息

Otolaryngol Head Neck Surg. 1993 Nov;109(5):877-85. doi: 10.1177/019459989310900517.

DOI:10.1177/019459989310900517
PMID:8247569
Abstract

Extramedullary plasmacytomas are solitary tumors consisting of neoplastic plasma cell proliferations that occur in locations other than bone. On initial presentation they must be differentiated from multiple myeloma. This may prove to be difficult because a varying percentage may be associated at a later date with the development of multiple myeloma. Solitary extramedullary plasmacytomas represent up to 4% of nonepithelial lesions of the upper respiratory tract. From 1970 to 1990, at West Virginia University Hospitals, seven patients with solitary extramedullary plasmacytoma were identified. In four of these patients the tumor was located in the head and neck, with one tumor located in each of the following sites: temporoparietal scalp, maxillary sinus, nasopharynx, and cervical region. One patient had extensive destruction of the temporal bone, with extension intracranially to the middle cranial fossa. No patient had multiple myeloma, nor did any develop. Diagnosis was based on a combination of histology along with special immunoperoxidase staining for Ig lambda and kappa light chains. This will be demonstrated and discussed. Treatment consisted of radiotherapy in three cases, with doses ranging from 3175 to 6000 rad. One patient, treated with surgical excision, experienced a relapse at a distant site 6 years later. All patients have maintained local control and have been followed for a minimum of 1 1/2 years, with an average of 3 years. We describe our experience with these tumors and present a pertinent review of the literature. While these tumors may present as aggressive locally destructive lesions, their management should be as organ-sparing as possible because excellent control can be achieved in the majority of cases.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

髓外浆细胞瘤是由肿瘤性浆细胞增殖形成的孤立性肿瘤,发生于骨骼以外的部位。初诊时必须将其与多发性骨髓瘤相鉴别。这可能颇具难度,因为不同比例的患者日后可能会发展为多发性骨髓瘤。孤立性髓外浆细胞瘤占上呼吸道非上皮性病变的4%。1970年至1990年期间,在西弗吉尼亚大学医院,共确诊7例孤立性髓外浆细胞瘤患者。其中4例患者的肿瘤位于头颈部,分别位于以下部位:颞顶部头皮、上颌窦、鼻咽部和颈部。1例患者颞骨广泛破坏,颅内延伸至中颅窝。所有患者均无多发性骨髓瘤,也未发展为多发性骨髓瘤。诊断基于组织学检查以及针对Ig λ和κ轻链的特殊免疫过氧化物酶染色。将对此进行展示和讨论。3例患者接受放射治疗,剂量为3175至6000拉德。1例接受手术切除的患者6年后在远处部位复发。所有患者均维持局部控制,随访时间最短为1年半,平均为3年。我们描述了我们对这些肿瘤的治疗经验,并对相关文献进行了综述。虽然这些肿瘤可能表现为侵袭性局部破坏性病变,但在大多数情况下应尽可能采取保留器官的治疗方法,因为可以实现良好的控制效果。(摘要截取自250字)

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