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A Case of Neurofibromatosis Type 1 Coinciding with Bilateral Pheochromocytomas, Multiple Gastrointestinal Stromal Tumors, and Malignant Peripheral Nerve Sheath Tumor

机译:一例伴有双侧嗜铬细胞瘤,多发胃肠道间质瘤和恶性周围神经鞘瘤的1型神经纤维瘤病病例

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Neurofibromatosis type 1 (NF1) is associated with benign and malignant neoplasms, but the coincidence of abdominal neoplasms is rare. A 65-year-old woman with NF1 had episodes of nausea, tachycardia, hypertension, and loss of consciousness. Bilateral adrenal tumors were detected by abdominal computed tomography, and plasma and urinary catecholamine levels were elevated. Open bilateral adrenalectomy and histological findings revealed bilateral pheochromocytomas (PCCs). Furthermore, malignant peripheral nerve sheath tumor (MPNST) and multiple gastrointestinal stromal tumors (GISTs) were incidentally found in the abdominal cavity. Early diagnosis of abdominal neoplasms in NF1 patients is important because of the risk of malignancy, organic complications and hemorrhagic-obstructive complications.
机译:1型神经纤维瘤病(NF1)与良性和恶性肿瘤有关,但腹部肿瘤的巧合很少见。一名患有NF1的65岁女性有恶心,心动过速,高血压和意识丧失的发作。通过腹部计算机断层扫描检测到双侧肾上腺肿瘤,血浆和尿儿茶酚胺水平升高。开放性双侧肾上腺切除术,组织学发现双侧嗜铬细胞瘤(PCC)。此外,在腹腔中偶然发现了恶性周围神经鞘瘤(MPNST)和多种胃肠道间质瘤(GIST)。由于恶性肿瘤,器质性并发症和出血性阻塞性并发症的风险,NF1患者腹部肿瘤的早期诊断很重要。

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