罕见的共存:乳腺癌、嗜铬细胞瘤和冯-雷克林豪森氏病

Letaief Sarra Ben, Zemni Ines, Saadallah Fatma, Ghalleb Montassar, Sahraoui Ghada, Ayadi Mohamed Ali, Dhieb Tarek
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摘要

与 1 型神经纤维瘤病相关的乳腺癌是一种罕见的临床实体。这些患者罹患各种癌症的风险较高,尤其是来自胚胎神经嵴的肿瘤,如嗜铬细胞瘤。本出版物旨在为 1 型神经纤维瘤病、乳腺癌和嗜铬细胞瘤之间的罕见关联提供更多文献资料。我们介绍了一例罕见病例:一名 51 岁的突尼斯女性神经纤维瘤患者被诊断出患有乳腺癌和嗜铬细胞瘤。乳腺肿瘤被归类为 T4b N1M0,而嗜铬细胞瘤是在胸腹盆腔 CT 中偶然发现的。她接受了肾上腺切除手术,并被转诊至肿瘤内科医生处接受乳腺癌化疗。1 型神经纤维瘤病是一种良性疾病,但患者可能会患上多种肿瘤。早期诊断具有挑战性,会使预后恶化,增加医疗难度。
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A Rare Coexistence: Breast Cancer, Pheochromocytoma and Von Recklinghausen Disease
Breast cancer associated with type-1 neurofibromatosis is a rare clinical entity. These patients have a higher risk of developing various types of cancers, especially tumors derived from the embryogenic neural crest, such as pheochromocytoma. This publication aims to add to the literature a rare association between Type-1 Neurofibromatosis, breast cancer, and pheochromocytoma. We present a rare case of a 51-year-old Tunisian woman with neurofibromatosis who was diagnosed with breast cancer and pheochromocytoma. The breast tumor was classified as T4b N1M0, and the discovery of the pheochromocytoma was incidental to thoracic-abdominal-pelvic CT. She underwent surgery to remove the adrenal gland and was referred to medical oncologists to receive chemotherapy for her breast cancer. Type-1 Neurofibromatosis disorder is a benign disease but can expose patients to numerous neoplasms. The challenging diagnosis at an early stage can worsen the prognosis and make medical care more difficult.
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