舌头间质肿瘤:93 例临床病理学研究。

IF 2.7 2区 医学 Q2 PATHOLOGY Human pathology Pub Date : 2024-06-12 DOI:10.1016/j.humpath.2024.06.005
Domenika Ortiz Requena , Jaylou M. Velez-Torres , Julio A. Diaz-Perez , Carmen Gomez-Fernandez , Elizabeth A. Montgomery , Andrew E. Rosenberg
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引用次数: 0

摘要

舌肿瘤比较常见,绝大多数是上皮性肿瘤。尽管并不常见,但在这个解剖部位也会出现多种多样、各具特色的间叶肿瘤。为了增加我们对这些病变的了解,我们回顾了我们对舌间质瘤的经验,并描述了它们的临床病理特征。我们查询了 2005-2021 年的病理档案和其中一位作者的会诊档案,以了解所有舌 MNs 的情况。我们查看了组织学切片和辅助研究,并从现有病历中获取了临床数据。我们发现了 93 例患者,他们构成了研究队列--据我们所知,这是最大的舌间叶肿瘤系列。四十八例患者为女性,四十五例为男性,平均年龄为 51 岁(范围:1-94 岁)。这些肿瘤包括 43 个(46.2%)血管瘤、14 个(15%)颗粒细胞瘤、8 个(9%)脂肪瘤、4 个(4.3%)裂隙瘤、4 个(4.3%)单纤维瘤--根据风险分层标准,这些肿瘤的恶化风险都很低;2 个(2.2%)淋巴管瘤,3(3.2%)卡波西肉瘤,2(2.2%)软骨瘤,2(2.2%)肌纤维瘤,1(1.1%)单发环形神经瘤,1(1.1(1.1%)会厌瘤,1(1.1%)神经纤维瘤,1(1.1%)外生性软骨瘤,1(1.1%)伴有 NOTCH2 重排和 TLL2 突变的非典型胶质瘤,1(1.1(1.1%)纺锤形细胞横纹肌肉瘤;1(1.1%)多形性成纤维肉瘤;1(1.1%)恶性横纹肌瘤;1(1.1%)亮肌肉瘤;1(1.1%)血管肉瘤;1(1.1%)肺泡软组织肉瘤。大部分患者接受了手术切除,1 名患者(血管瘤)接受了栓塞治疗。在随访中,纺锤细胞横纹肌肉瘤患者术后出现手术部位麻木,随访17个月后不再发病。而患有骨髓纤维肉瘤的患者拒绝了辅助放射治疗,并在22个月时出现了肺部转移。肺泡软组织肉瘤患者在确诊时已出现肺部转移,接受了辅助化疗。其余患者均无局部或远处复发。舌头上的多发性肉瘤通常是良性的,以内皮细胞、脂肪细胞或分裂细胞分化为特征。治疗的主要方法是手术切除,切除范围由肿瘤类型决定。辅助治疗适用于高级别肉瘤。
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Mesenchymal neoplasms of the tongue: A clinicopathologic study of 93 cases

Neoplasms of the tongue are relatively common, and the vast majority are epithelial in phenotype. Although uncommon, a diverse and distinctive array of mesenchymal neoplasms arises in this anatomic site. To increase our understanding of these lesions, we reviewed our experience of MNs of the tongue and described their clinicopathologic features. The pathology archives from 2005 to 2021 and the consultation files of one of the authors were queried for all MNs of the tongue. We reviewed the histologic slides and ancillary studies and obtained clinical data from the available medical records. Ninety-three cases were identified, and they form the study cohort - to our knowledge, this is the largest series of mesenchymal neoplasms of the tongue. Forty-eight patients were female, and forty-five were male, with a mean age of 51 years (range: 1–94 years). The tumors included 43 (46.2%) hemangiomas, 14 (15%) granular cell tumors, 8 (9%) lipomas, 4 (4.3%) schwannomas, 4 (4.3%) solitary fibrous tumors - all with low risk of progression based on risk stratification criteria, 2 (2.2%) lymphangiomas, 3 (3.2%) Kaposi sarcomas, 2 (2.2%) chondromas, 2 (2.2%) myofibromas, 1 (1.1%) solitary circumscribed neuroma, 1 (1.1%) perineurioma, 1 (1.1%) neurofibroma, 1 (1.1%) ectomesenchymal chondromyxoid tumor, 1 (1.1%) atypical glomus tumor with a NOTCH2 rearrangement and TLL2 mutation, 1 (1.1%) spindle cell rhabdomyosarcoma, 1 (1.1%) pleomorphic fibroblastic sarcoma, 1 (1.1%) malignant rhabdoid tumor, 1 (1.1%) leiomyosarcoma, 1 (1.1%) angiosarcoma, and 1 (1.1%) alveolar soft part sarcoma. Most of the patients underwent surgical excision, and 1 patient (with hemangioma) underwent embolization. On follow-up, the patient with spindle cell rhabdomyosarcoma developed postoperative numbness at the surgical site and was disease-free through 17 months of follow-up. The patient with leiomyosarcoma declined adjuvant radiation and developed metastasis to the lung at 22 months. The patient with alveolar soft part sarcoma had metastases to the lung at the time of diagnosis and received adjuvant chemotherapy. The remaining patients had no local or distant recurrence. MNs of the tongue are usually benign and characterized by either endothelial, adipocytic, or schwannian differentiation. The mainstay of treatment is surgical excision with the extent of excision determined by tumor type. Adjuvant therapy is reserved for high-grade sarcomas.

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来源期刊
Human pathology
Human pathology 医学-病理学
CiteScore
5.30
自引率
6.10%
发文量
206
审稿时长
21 days
期刊介绍: Human Pathology is designed to bring information of clinicopathologic significance to human disease to the laboratory and clinical physician. It presents information drawn from morphologic and clinical laboratory studies with direct relevance to the understanding of human diseases. Papers published concern morphologic and clinicopathologic observations, reviews of diseases, analyses of problems in pathology, significant collections of case material and advances in concepts or techniques of value in the analysis and diagnosis of disease. Theoretical and experimental pathology and molecular biology pertinent to human disease are included. This critical journal is well illustrated with exceptional reproductions of photomicrographs and microscopic anatomy.
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