Salivary gland adenoid cystic carcinoma presenting as a large metastatic hepatic mass: a case report.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Journal of Medical Case Reports Pub Date : 2025-03-19 DOI:10.1186/s13256-025-05151-z
Matthew Walker, Alisa Dewald, Abdelrhman Refaey, Ivan Berezowski, Jacob Newman, Mamoun Younes, Stephen Gray
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Abstract

Background: Salivary gland tumors are rare, representing 6-8% of head and neck tumors. Adenoid cystic carcinoma represents approximately 10% of salivary gland tumors. The preferential sites of metastases are the lung and bone, followed by the brain and liver. Liver metastasis as the initial clinical manifestation of parotid gland adenoid cystic carcinoma is very rare.

Case presentation: We report the case of a 29-year-old African American male patient with a metastatic salivary gland tumor who presented initially with a large hepatic mass. He complained of right upper quadrant pain and early satiety. Abdominal computed tomography revealed hepatomegaly with a large mass centered in the left lobe measuring 14 cm. A computed tomography scan revealed innumerable bilateral pulmonary nodules measuring up to 8 mm, favoring metastases. Initial histopathological examination of the liver biopsy specimens revealed a well-differentiated carcinoma characterized by a distinctive myxoid stroma, consistent with metastatic adenoid cystic carcinoma. The patient underwent transcatheter arterial chemoembolization and was discharged with a hematology-oncology follow-up. A presumptive diagnosis of stage IV adenoid cystic carcinoma with lung and liver metastases was made. The patient was given cisplatin and vinorelbine.

Conclusion: Metastatic parotid gland adenoid cystic carcinoma with initial clinical manifestation as a liver mass is very rare and was pathologically confirmed in this patient by its histological appearance. This case emphasizes the need for clinicians to consider salivary gland tumors in the differential diagnosis of unexplained hepatic lesions.

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涎腺腺样囊性癌表现为大转移性肝脏肿块1例。
背景:唾液腺肿瘤是罕见的,占头颈部肿瘤的6-8%。腺样囊性癌约占唾液腺肿瘤的10%。转移的首选部位是肺和骨,其次是脑和肝。以肝转移为首发临床表现的腮腺腺样囊性癌是非常罕见的。病例介绍:我们报告一例29岁的非裔美国男性患者的转移性唾液腺肿瘤最初表现为一个大的肝脏肿块。他主诉右上腹疼痛和早饱。腹部计算机断层扫描显示肝脏肿大,以左叶为中心的大肿块,直径14厘米。计算机断层扫描显示无数双侧肺结节,直径达8mm,有利于转移。肝活检标本的初步组织病理学检查显示为分化良好的癌,其特征为独特的黏液样间质,与转移性腺样囊性癌一致。患者接受了经导管动脉化疗栓塞,出院时进行了血液肿瘤学随访。推测诊断为IV期腺样囊性癌伴肺和肝转移。患者给予顺铂和长春瑞滨。结论:转移性腮腺腺样囊性癌最初临床表现为肝脏肿块是非常罕见的,本例患者的组织学表现病理证实。本病例强调临床医生需要考虑涎腺肿瘤在鉴别诊断不明原因的肝脏病变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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