basal cell adenoma

基底细胞腺瘤
  • 文章类型: Journal Article
    背景:基底细胞腺瘤(BCA)是一种罕见的唾液腺良性肿瘤。基底细胞腺癌(BCAC),BCA的恶性对应物,也是一种非常罕见的肿瘤,临床研究非常有限。本研究旨在探讨其临床特点,人口统计,腮腺内诊断为BCA和BCAC的患者的手术结果。
    方法:2003年5月至2023年8月对所有接受腮腺切除术的患者进行了回顾性分析。关于性别的回顾性数据,年龄,肿瘤特征,并收集结果。手术方法,包括实现负利润率,胶囊移除,和组织学诊断,也是详细的。
    结果:该研究包括1268例接受腮腺切除术的患者,导致81例BCA和7例BCAC。BCA患者,平均年龄55.1岁,显示出不同的年龄分布,主要出现在50年代。在BCAC案例中,七名女性患者在深叶中表现出主要位置。FNA在7例病例中发现了BCAC,随后进行了腮腺切除术,导致未观察到复发或转移。
    结论:这项研究报告了单个机构中数量最多的BCA病例,并提供了对人口统计学的全面见解,肿瘤特征,以及BCA和BCAC的临床结果。虽然需要进一步的研究,根据临床随访结果,在肿瘤切除术中适当地包括胶囊表明有利的结果,特别是当肿瘤大小不大时。
    BACKGROUND: Basal cell adenoma (BCA) is a rare benign tumor within the salivary glands. Basal cell adenocarcinoma (BCAC), the malignant counterpart of BCA, is also an exceedingly rare tumor with very limited clinical studies conducted. This study aims to investigate the clinical characteristics, demographics, and surgical outcomes of patients diagnosed with BCA and BCAC within the parotid gland.
    METHODS: A retrospective analysis from May 2003 to August 2023 was performed for all patients undergoing parotidectomy for masses. Retrospective data on gender, age, tumor characteristics, and outcomes were collected. Surgical approaches, including negative margin attainment, capsule removal, and histological diagnosis, were also detailed.
    RESULTS: The study included 1268 patients who underwent parotidectomy, resulting in 81 cases of BCA and 7 cases of BCAC. BCA patients, with a mean age of 55.1 years, showed diverse age distribution and predominantly presented in the 50s. In BCAC cases, seven female patients exhibited a predominant location in the deep lobes. FNA revealed BCAC in three out of seven cases, and subsequent parotidectomy was performed, resulting in no observed recurrences or metastases.
    CONCLUSIONS: This study reports the largest number of BCA cases from a single institution and provides comprehensive insights into the demographics, tumor characteristics, and clinical outcomes of both BCA and BCAC. Although further research should be conducted, based on clinical follow-up results, appropriately including the capsule in the tumor excision indicates favorable outcomes, especially when the tumor size is not large.
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  • 文章类型: Case Reports
    基底细胞腺瘤(BCA)是一种罕见的,起源于唾液腺上皮细胞的良性肿瘤。较早被归类为具有独特组织病理学特征的单形性腺瘤的亚型。BCA通常表现为无症状,生长缓慢的肿块表现出部位和年龄偏好,通常影响老年女性患者的主要唾液腺。组织学上,固体,小梁,管状,膜状图案被识别。必须在BCA之间建立精确的区别,多形性腺瘤,和恶性唾液腺肿瘤开始治疗前,以确保有效的管理。标准治疗方法是手术切除肿瘤。复发和恶性转化很少发生,除了膜质亚型。本文旨在报告一例由上唇的小唾液腺引起的BCA异常病例。手术后的过程并不引人注目,手术部位完全愈合。在一年的随访中没有观察到复发。由上唇的小唾液腺引起的BCA是一种极为罕见的实体。全面回顾上唇的BCA,从1991年到2023年12月报告,只有14例。
    Basal cell adenoma (BCA) is a rare, benign tumor originating from the epithelial cells of the salivary glands. It was earlier categorized as a subtype of monomorphic adenoma with distinctive histopathological features. BCA usually manifests as asymptomatic, slow-growing masses that exhibit a site and age predilection, commonly affecting the major salivary glands of elderly female patients. Histologically, solid, trabecular, tubular, and membranous patterns are recognized. It is imperative to establish a precise distinction between BCA, pleomorphic adenoma, and malignant salivary gland tumors before initiating treatment to ensure effective management. The standard treatment approach is surgical resection of the tumor. Recurrence and malignant transformation rarely occur, except for the membranous subtype. This article aims to report an unusual case of BCA arising from a minor salivary gland in the upper lip. The post-operative course was unremarkable, with complete healing of the surgical site. No recurrence was observed during a one-year follow-up. BCA arising from a minor salivary gland in the upper lip is an extremely uncommon entity. A comprehensive review of BCA in the upper lip, reported from 1991 to December 2023, revealed only 14 cases.
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  • 文章类型: Journal Article
    目的:TRPS1是一个新的,乳腺癌敏感标志物(BC)。唾液腺和乳房都是外分泌腺;因此,它们的肿瘤可能具有相似的形态和免疫表型。在唾液腺型BC中,据报道,TRPS1在分泌性癌(SC)中呈阳性,但在腺泡细胞癌(AcCC)和大多数腺样囊性癌(AdCC)中呈阴性。唾液导管癌(SDC)的一个子集对TRPS1呈阳性。在这里,我们研究了TRPS1免疫组织化学在唾液腺肿瘤(SGT)中的表达。
    方法:回顾性检索得到110SGT(原发97例,转移13例)。TRPS1免疫组织化学评分为阴性,低正,中间积极,或强烈的积极。
    结果:TRPS1在78%(14/18)的多形性腺瘤(PA)病例中表达,但在所有Warthin肿瘤中均为阴性/低阳性(6/6[100%])。在基底细胞腺瘤(BCA)中,TRPS1在基质细胞中的表达是中等到强(13/14[92%]),而导管或基底细胞显示低表达。TRPS1在恶性SGT中的表达不同,在100%(15/15)的AdCC中有中等至强染色,100%(5/5)的基底细胞腺癌,100%(3/3)的导管内癌,89%(8/9)的多形性腺癌,89%(7/8)的SDCs;在100%(3/3)的SCs中观察到阴性/低阳性表达,89%(8/9)的AcCC,和50%(3/3)的粘液表皮样癌。此外,在转移到肺的SGT中观察到强和中等的TRPS1表达,淋巴结,和软组织。
    结论:总体而言,TRPS1在PA以及恶性和转移性SGT中强烈表达。此外,TRPS1在BCA基质细胞中呈阳性,但在导管和基底细胞中呈阴性或低阳性。
    OBJECTIVE: TRPS1 is a new, sensitive marker for breast carcinoma (BC). Salivary glands and breasts are both exocrine glands; thus, their tumors may share similar morphology and immunophenotype. Among salivary gland-type BC, TRPS1 is reported to be positive in secretory carcinomas (SCs) but negative in acinic cell carcinomas (AciCCs) and most adenoid cystic carcinomas (AdCCs). A subset of salivary duct carcinomas (SDCs) is positive for TRPS1. Herein, we investigate TRPS1 immunohistochemical expression in salivary gland tumors (SGTs).
    METHODS: A retrospective search yielded 110 SGTs (97 primary and 13 metastatic). TRPS1 immunohistochemistry was scored as negative, low positive, intermediate positive, or strongly positive.
    RESULTS: TRPS1 was expressed in 78% (14/18) of pleomorphic adenoma (PA) cases but negative/low positive in all Warthin tumors (6/6 [100%]). In basal cell adenoma (BCA), TRPS1 expression was intermediate to strong (13/14 [92%]) in the stromal cells, whereas ductal or basal cells showed low expression. TRPS1 expression varied in malignant SGTs, with intermediate to strong staining in 100% (15/15) of AdCCs, 100% (5/5) of basal cell adenocarcinoma, 100% (3/3) of intraductal carcinoma, 89% (8/9) of polymorphous adenocarcinoma, and 89% (7/8) of SDCs; negative/low positive expression was observed in 100% (3/3) of SCs, 89% (8/9) of AciCCs, and 50% (3/3) of mucoepidermoid carcinomas. In addition, strong and intermediate TRPS1 expression was observed in metastatic SGT to the lungs, lymph nodes, and soft tissue.
    CONCLUSIONS: Overall, TRPS1 is strongly expressed in PA as well as malignant and metastatic SGT. In addition, TRPS1 is positive in stromal cells of BCA but negative or low positive in ductal and basal cells.
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  • 在某些类型的唾液腺肿瘤中很少报道梗塞。在这项研究中,我们介绍了第一例发生于唾液基底细胞腺瘤的梗死。一名62岁的男性出现左侧腮腺区域肿胀。组织病理学检查显示,广泛的中央坏死被有活力的肿瘤组织边缘包围,显示了基底细胞腺瘤的典型组织学。在肿瘤中鉴定了核β-连环蛋白表达和CTNNB1p.I35T(c.104T>C)突变。诊断为基底细胞腺瘤伴中央坏死,术后时间顺利。此外,我们回顾了唾液腺基底细胞肿瘤中CTNNB1I35T突变的文献。了解梗死的可能发生和基底细胞腺瘤中独特突变的高频率可能有助于唾液腺肿瘤的鉴别诊断。
    Infarction has rarely been reported in some types of salivary gland tumors. In this study, we present the first case of infarction occurring in salivary basal cell adenoma. A 62-year-old male presented with swelling in the left parotid region. Histopathological examination revealed extensive central necrosis surrounded by a rim of viable tumor tissue showing the typical histology of basal cell adenoma. Nuclear β-catenin expression and the CTNNB1 p.I35T (c.104 T > C) mutation were identified in the tumor. A diagnosis of basal cell adenoma with central necrosis was made, and the postoperative period was uneventful. In addition, we review the literature on CTNNB1 I35T mutations in basal cell neoplasms of the salivary glands. Awareness of the possible occurrence of infarction and the high frequency of the unique mutation in basal cell adenoma may help in the differential diagnosis of salivary gland tumors.
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  • 文章类型: Case Reports
    基底细胞腺瘤是一种罕见的腮腺良性肿瘤病变,因此,在术前检查中很少通过细针穿刺细胞学检查来诊断。这种独特的实体被认为是罕见的唾液肿瘤之一,主要在女性人群中被感知。但在年轻人中并不常见。在细胞病理学上诊断主要是唾液腺基底细胞腺瘤的基底细胞样肿瘤极具挑战性。因此,本病例报告描述了40岁女性左腮腺基底细胞腺瘤的细针穿刺细胞学诊断。病例报告还描述了细胞形态学特征,基底细胞腺瘤的细胞学鉴别诊断和免疫组织化学。
    Basal cell adenoma is a rare benign neoplastic lesion of the parotid gland, therefore it is rarely diagnosed in preoperative work-up by fine needle aspiration cytology. This distinctive entity being regarded as one of the scarce salivary neoplasms is predominantly perceived in the female population, but is uncommon in young adults. It is extremely challenging to diagnose basaloid tumors predominantly basal cell adenoma of the salivary gland on cytopathology. Therefore present case report describes the fine needle aspiration cytology diagnosis of basal cell adenoma in the left parotid gland in a 40-year-old female. The case report also describes the cytomorphological characters, the cytological differential diagnoses and immunohistochemistry of basal cell adenoma.
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  • 文章类型: Case Reports
    唾液腺的肿瘤很少发生,有一个模糊的介绍,并遵循复杂的长期临床过程。小唾液腺和大唾液腺都与发育不良转化有关,以腮腺肿瘤最为显著。这些肿瘤中的大多数本质上是良性的,并且通常基于它们的组织病理学表现来诊断和分类。在这份报告中,我们表现为基底细胞腺瘤(BCA)的罕见病例,位于右侧腮腺,一名69岁的男性患者。在有和没有对比的情况下获得该区域的体积采集计算机断层扫描(CT)成像,在冠状面和轴向平面都有相对重建。在右腮腺浅叶中检测到直径为5cm的软组织肿块。超声引导下的细针抽吸(FNA)显示出一群单形的基底细胞,具有最小的核异型性和分散的原纤维基质。此后,患者在全身麻醉下接受右腮腺部分切除术治疗,术后病理报告证实为基底细胞腺瘤。患者术后表现良好,无投诉,并保持常规临床随访。
    Neoplasms of the salivary glands are of rare incidence, have a vague presentation, and follow a complex long-term clinical course. Both minor and major salivary glands have been implicated in dysplastic transformation, with parotid gland tumors being the most notable. Most of these tumors are benign in nature and are typically diagnosed and classified based on their histopathological presentation. In this report, we exhibit a rare case of basal cell adenomas (BCA), localized to the right parotid gland, in a 69-year-old male patient. Volume acquisition computed tomography (CT) imaging of the region was obtained with and without contrast, with relative reconstruction in both the coronal and axial planes. A soft tissue mass of 5 cm in diameter was detected in the superficial lobe of the right parotid gland. Fine needle aspiration (FNA) with ultrasound guidance revealed a population of basaloid cells that is monomorphic with minimal nuclear atypia and scattered fibrillary matrix. Thereafter, the patient was treated with partial excision of the right parotid gland under general anesthesia, and the post-operative pathology report confirmed the diagnosis of basal cell adenoma. The patient was doing well post-operatively with no complaints and maintained routine clinic follow-ups.
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  • 文章类型: Case Reports
    一种罕见的唾液腺肿瘤被称为基底细胞腺瘤(BCA)。只有一小部分唾液腺肿瘤影响口腔的小唾液腺,而大多数在腮腺中发现。我们介绍了一例罕见的BCA病例,涉及一名45岁女性的左颊粘膜。磁共振成像(MRI)显示,左颊空间与颊肌分不开,大小为1.9x1.5cm。T2加权图像显示了对比后的高强度信号。超声引导的细针穿刺细胞学检查显示,恶性潜能不确定的细胞基底细胞样肿瘤。此后,在全身麻醉下通过经口方法切除肿块。肿块的组织病理学显示包裹的基底细胞肿瘤有利于BCA。患者术后情况良好,面神经及耳廓颞神经、耳大神经等邻近神经完整,无并发症,并进行常规临床随访,手术部位成功恢复。因此,我们的结论是MRI和活检为鉴别良性腺瘤和恶性腺癌提供了有用的信息.在孤立性颈部肿块的鉴别诊断中应考虑BCA。手术切除显示出良好的预后。
    One of the rare tumors of the salivary gland is known as basal cell adenoma (BCA). Only a small percentage of salivary gland tumors affect the minor salivary gland of the oral cavity while the majority are found in the parotid gland. We present a rare case of BCA involving the left buccal mucosa of a 45-year-old female. Magnetic resonance imaging (MRI) showed well defined solid mass measuring 1.9 x 1.5 cm in the left buccal space inseparable from the buccinator muscle. The T2-weighted image demonstrates a hyperintense signal post-contrast. Ultrasound-guided fine needle aspiration cytology revealed cellular basaloid neoplasm of uncertain malignant potential. Thereafter excision of the mass was performed through a transoral approach under general anesthesia. Histopathology of the mass showed encapsulated basal cell neoplasm in favor of BCA. The patient was doing well after the surgery and has intact facial nerve and adjacent nerves such as the auriculotemporal nerve and great auricular nerve with no complications then she kept on routine clinic follow-ups, and the surgical site recovered successfully. Therefore, we conclude that MRI and biopsy provide useful information to differentiate between benign adenoma and malignant adenocarcinoma. BCA should be considered in a differential diagnosis of an isolated neck mass. Surgical excision demonstrates an excellent prognosis.
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  • 文章类型: Case Reports
    一名65岁的女性患者,有15年戴义齿的历史,报告说口腔底部疼痛。在检查中,在左侧的口腔底部注意到约2.2X1.2cms的肿胀。在局部麻醉下切除病灶。组织病理学显示囊性病变,小管中排列有基底细胞,巢和筛状图案。诊断为基底细胞腺瘤,并通过免疫组织化学证实。我们报告了一种罕见的模仿ranula的口腔底基底细胞腺瘤。这种基底细胞样肿瘤的主要囊性构成了诊断挑战。组织病理学和免疫组织化学分析,以获得明确的诊断,有助于治疗计划和预后。
    A 65-year-old female patient with a history of wearing a denture for 15 years reported with a complaint of pain in the floor of the mouth. On examination, a swelling measuring about 2.2 X1.2 cms was noted in the floor of the mouth on the left side. The lesion was excised under local anesthesia. Histopathology revealed a cystic lesion with basaloid cells arranged in tubules, nests and cribriform pattern. A diagnosis of basal cell adenoma was made and confirmed by immunohistochemistry. We report a rare case of Basal Cell Adenoma of the floor of the mouth which mimicked a ranula. The predominantly cystic nature of this basaloid tumor posed a diagnostic challenge. Histopathological and immunohistochemical analysis to arrive at a definitive diagnosis aid in treatment planning and prognostication.
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  • 文章类型: Journal Article
    鼻腔或鼻旁窦引起的基底细胞腺瘤(BCA)非常罕见。一名64岁的男性患者在接受术前计算机断层扫描和磁共振成像后被怀疑患有恶性肿瘤。术中冰冻切片显示恶性肿瘤;然而,最终诊断显示BCA有异型性,管状图案。
    Basal cell adenomas (BCA) arising from the nasal cavity or paranasal sinuses are very rare. A 64-year-old male patient was suspected of having a malignant tumor after undergoing preoperative computed tomography scans and magnetic resonance imaging. The intraoperative frozen section showed a malignant tumor; however, the final diagnosis revealed BCA with atypia, tubular pattern.
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  • 文章类型: Journal Article
    腺样囊性癌(ACC)是最常见的原发性涎腺癌之一。ACC在唾液腺肿瘤中有几种良性和恶性模拟物。ACC的准确诊断对于患者的最佳管理及其随访至关重要。已经在ACC的85-90%中描述了MYB的上调,但在其他唾液腺肿瘤中没有。在ACC,MYB上调可作为遗传重排t(6;9)(q22-23;p23-24)的结果,MYB拷贝数变异(CNV),或增强剂劫持MYB。MYB上调的所有机制导致RNA转录增加,这可以使用RNA原位杂交(ISH)方法检测。在这项研究中,利用138个原发性唾液腺肿瘤,包括78个ACC,我们评估了MYBRNAISH用于区分ACC与其他具有突出筛状结构的原发性唾液腺肿瘤(包括多形性腺瘤)的诊断实用性。基底细胞腺瘤,基底细胞腺癌,上皮性肌上皮癌,和多形性腺癌。还进行了荧光原位杂交和下一代测序以评估当存在MYB基因改变时,RNAISH检测增加的MYBRNA的敏感性和特异性。MYBRNA的检测对于在唾液腺肿瘤中诊断ACC具有92.3%的灵敏度和98.2%的特异性。ISH检测MYBRNA的灵敏度(92.3%)明显高于FISHMYB分解探针(42%)对ACC的灵敏度。在缺乏MYBRNA过表达的情况下,下一代测序未显示MYB改变,表明MYBRNAISH对检测MYB基因改变的高灵敏度。与具有RNA降解的较旧的回顾性组织样品相比,在临床实践中使用当代样品的灵敏度可能更高的可能性并不完全排除。除了高灵敏度和特异性,MYBRNA测试可以使用标准IHC平台和方案进行,并使用明场显微镜进行评估,使其成为常规临床实践中具有时间和成本效益的诊断工具。
    Adenoid cystic carcinoma (ACC) is one of the most common primary salivary gland cancers. ACC has several benign and malignant mimics amongst salivary gland neoplasms. An accurate diagnosis of ACC is essential for optimal management of the patients and their follow-up. Upregulation of MYB has been described in 85-90% of ACC, but not in other salivary gland neoplasms. In ACC, MYB upregulation can occur as a result of a genetic rearrangement t(6;9) (q22-23;p23-24), MYB copy number variation (CNV), or enhancer hijacking of MYB. All mechanisms of MYB upregulation result in increased RNA transcription that can be detected using RNA in situ hybridisation (ISH) methods. In this study, utilising 138 primary salivary gland neoplasms including 78 ACC, we evaluate the diagnostic utility of MYB RNA ISH for distinguishing ACC from other primary salivary gland neoplasms with a prominent cribriform architecture including pleomorphic adenoma, basal cell adenoma, basal cell adenocarcinoma, epithelial myoepithelial carcinoma, and polymorphous adenocarcinoma. Fluorescent in situ hybridisation and next generation sequencing were also performed to evaluate the sensitivity and specificity of RNA ISH for detecting increased MYB RNA when MYB gene alterations were present. Detection of MYB RNA has 92.3% sensitivity and 98.2% specificity for a diagnosis of ACC amongst salivary gland neoplasms. The sensitivity of MYB RNA detection by ISH (92.3%) is significantly higher than that of the FISH MYB break-apart probe (42%) for ACC. Next generation sequencing did not demonstrate MYB alterations in cases that lacked MYB RNA overexpression indicating high sensitivity of MYB RNA ISH for detecting MYB gene alterations. The possibility that the sensitivity may be higher in clinical practice with contemporary samples as compared with older retrospective tissue samples with RNA degradation is not entirely excluded. In addition to the high sensitivity and specificity, MYB RNA testing can be performed using standard IHC platforms and protocols and evaluated using brightfield microscopy making it a time and cost-efficient diagnostic tool in routine clinical practice.
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