成人发病型胰腺神经母细胞瘤:病例报告与文献综述

Q4 Medicine Radiology Case Reports Pub Date : 2024-11-06 DOI:10.1016/j.radcr.2024.10.066
Noufel Alshadood , Ali Naser Aldarawsha , Sajjad Ghanim Al-Badri , Mohamed Samy Elazab , Manar Mohammed Mahdi , Flayyih Hasan Yousif , Asdah Alawad , Nabeel Al-Fatlawi , Abbas Hamza Abbas , Alaa Saeed AbdAli
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引用次数: 0

摘要

神经母细胞瘤是一种侵袭性恶性肿瘤,常见于儿童,成年患者相当罕见。即使在成人病例中,胰腺神经母细胞瘤也尤为罕见。我们介绍了一例 26 岁女性患者的病例,她因轻微腹痛和可触及的肿块被诊断为胰腺神经母细胞瘤。经过初步诊断后,活检证实了神经母细胞瘤的诊断。此后,患者接受了一个疗程的新辅助化疗,随后进行了复杂的手术切除。该病例强调了综合诊断方法的重要性,包括反复活检和多学科团队参与治疗罕见的成人神经母细胞瘤。
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Adult-onset pancreatic neuroblastoma: A case report with a literature review
Neuroblastoma is an aggressive malignancy commonly found in children, with adult patients being quite rare. Pancreatic neuroblastoma, even among adult cases, is especially rare. We present a case of a 26-year-old woman presented with mild abdominal pain and a palpable mass diagnosed as neuroblastoma affecting the pancreas. After initial diagnostic challenges, a biopsy confirmed the diagnosis of neuroblastoma. The patient thereafter underwent a course of neoadjuvant chemotherapy, followed by a complex surgical resection. This case highlights the importance of a comprehensive diagnostic approach, including repeated biopsies and the involvement of a multidisciplinary team in the management of rare presentations of adult neuroblastoma.
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来源期刊
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
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