嗜瘤细胞瘤:一种令人费解的腮腺肿瘤

Md Abdullah Al Mamun, Md Rabiul Islam, Riashat Azim Majumder, Mohammad Nurul Amin, Md Asif Anowar, Md Rashid E Mahbub, Mohmmad Ashaduzzaman
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摘要

嗜瘤细胞瘤是一种罕见的唾液腺肿瘤,由嗜瘤细胞和许多增生性线粒体组成。它通常发生在腮腺。文献中很少报道腮腺嗜酸细胞瘤的病例。由于其罕见性(占唾液腺肿瘤的1-2%)和临床表现。由于嗜酸细胞瘤与其他良性和低度恶性唾液腺肿瘤相似,临床医生往往将其误诊为多形性腺瘤、血管瘤或其他形式的嗜酸细胞病,因此临床诊断往往具有挑战性。以前发表的文章都同意这种病变发生在腮腺上的事实。本文旨在回顾以前发表的腺细胞瘤病例,以更好地了解这种罕见的腮腺肿瘤的人口学,临床病理,放射学和组织学特征。在使用涉及两个不同数据库(google scholar和PubMed)的敏感搜索策略后,对英语文献进行了系统综述。共纳入9例。该肿瘤多出现于老年期,为生长缓慢的肿瘤(平均病程3.17年),女性比例略高(女性:男性=1.25:1)。大部分都在肺叶浅部,100%。传统的组织学变异只被报道过。所有病例均行完全手术切除,无复发或恶性转化报告。影像学检查诊断该病变为良性肿瘤。只有组织病理学检查才能证实。组织学检查确定为嗜瘤细胞瘤。此外,我们的目标是将这些病变如何需要全面的检查以及如何选择最佳治疗策略带到最前沿。中华医学杂志[j];6 (1): 30-36
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Oncocytoma: A Mystifying Parotid Gland Tumour
Oncocytoma is a rare salivary gland tumor consisting of oncocytes with many hyperplastic mitochondria. It usually occurs in the parotid gland. Very few cases of parotid oncocytoma have been reported in literature. Because of its rarity (<1-2% of salivary gland tumors) and clinical presentation of the tumor. Clinical diagnosis is often challenging due to the likeness of oncocytoma to other benign and low-grade malignant salivary gland tumors there is a tendency among the clinicians to misdiagnose it as pleomorphic adenoma, hemangioma, or other forms of oncocytosis. Previously published articles had all agreed on the reality of this lesion occurring over the parotid gland. The paper aims to review previously published cases of oncoytoma to provide a better insight regarding demographic, clinicopathological, radiological and histological features of this rare tumor of parotid gland. A systemic review of English literature was performed after using a sensitive search strategy involving two different databases: google scholar and PubMed. A total number of 9 cases were included. The tumour is mostly presented in old age as a slowly growing tumour (mean duration 3.17 years) and showed a slightly higher female predominance (Female:Male=1.25:1). They were mostly located over superficial lobe,100%. Conventional histological variant has only been reported. Complete surgical excision was performed for all the cases without any reports of recurrence or malignant transformation. Imaging studies diagnosed the lesion as a benign tumor. Only histopathological examination can confirm it. Definitive histology examination concludes to oncocytoma. Furthermore, our aim is to bring to the forefront how these lesions require a comprehensive workup and how to choose the best treatment strategy. Mugda Med Coll J. 2023; 6(1): 30-36
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