维波玛

The patient was diagnosed with VIPoma, a rare neuroendocrine tumor that secretes vasoactive intestinal peptide.
病人被诊断为VIPoma，这是一种罕见的分泌血管活性肠肽的神经内分泌肿瘤。
A distinguishing feature of VIPoma is profuse watery diarrhea due to the excessive secretion of vasoactive intestinal polypeptide.
VIPoma的一个显著特征是由于血管活性肠多肽过度分泌导致的大量水样腹泻。
In cases of VIPoma, abdominal pain and flushing may also be present alongside the chronic diarrhea.
在VIPoma病例中，除了慢性腹泻外，也可能伴有腹痛和面部潮红症状。
Medical management for VIPoma includes symptom relief and addressing dehydration caused by the excessive diarrhea.
对于VIPoma的医疗管理包括缓解症状以及处理因严重腹泻引起的脱水问题。
Surgery is often the primary treatment for localized VIPoma to remove the tumor and alleviate symptoms.
对于局部性的VIPoma，手术通常是主要治疗手段，用于切除肿瘤并缓解症状。
Imaging studies such as CT scans and MRI are essential in locating the exact position of a suspected VIPoma.
如CT扫描和MRI等影像学研究对于确定疑似VIPoma的确切位置至关重要。
Biochemical tests can help confirm the diagnosis of VIPoma by identifying elevated levels of vasoactive intestinal peptide in the blood.
生化检测可以通过在血液中识别出血管活性肠肽水平升高来帮助确认VIPoma的诊断。
Treatment options for metastatic VIPoma include targeted therapies and chemotherapy to manage the spread of the disease.
对于转移性VIPoma，其治疗选项包括靶向疗法和化疗以控制疾病的扩散。
Early detection and prompt intervention are key to improving the prognosis for patients with VIPoma.
早期发现和及时干预对改善VIPoma患者预后至关重要。
Due to its rarity, it's crucial for physicians to consider VIPoma in the differential diagnosis of chronic secretory diarrhea.
由于VIPoma较为罕见，医生在鉴别诊断慢性分泌性腹泻时必须考虑到这一因素。