constitute
发表于 2025-3-28 15:37:09
http://reply.papertrans.cn/67/6641/664019/664019_41.png
嘴唇可修剪
发表于 2025-3-28 21:25:11
http://reply.papertrans.cn/67/6641/664019/664019_42.png
谄媚于性
发表于 2025-3-29 00:50:19
Functional Pancreatic Neuroendocrine Tumorsclinical symptoms secondary to that overproduction. They are a heterogeneous group of tumors in terms of their presentation, clinical syndromes, malignant potential, and management. Goals of treatment must focus on both their oncologic outcomes as well as the associated endocrinopathies. This chapte
蜡烛
发表于 2025-3-29 03:44:49
Jejunoileal Neuroendocrine Tumorsdence. Given the small intestine’s relative inaccessibility to endoscopy and the fact that SBNETs are frequently small, they often elude preoperative identification. Nodal and liver metastases are common at the time of diagnosis. The majority of SBNETs are low grade with slow growth, and with optima
CRP743
发表于 2025-3-29 08:39:07
http://reply.papertrans.cn/67/6641/664019/664019_45.png
Neuralgia
发表于 2025-3-29 11:37:13
http://reply.papertrans.cn/67/6641/664019/664019_46.png
PURG
发表于 2025-3-29 15:34:22
http://reply.papertrans.cn/67/6641/664019/664019_47.png
消瘦
发表于 2025-3-29 23:20:49
Medullary Thyroid Cancerrt of hereditary syndromes such as MEN2 with various clinical phenotypes dependent on the tumor genotype. The mainstays for treatment are early diagnosis and surgical removal of all disease. In the case of sporadic MTC, this is done with a total thyroidectomy and central lymph node dissection with a
肌肉
发表于 2025-3-30 03:50:26
Paraganglioma and Pheochromocytomapathetic paraganglia, respectively. Parasympathetic PGL are predominantly non-secreting and located in the head and neck and at the base of the skull (HNPGL), while sympathetic PGL are catecholamine-secreting and located in the abdomen and pelvis. Diagnostic work-up includes plasma or urinary metane
蹒跚
发表于 2025-3-30 07:52:27
Merkel Cell Carcinoma frequently in elderly Caucasian males on sun-exposed areas of the skin, and immunosuppression is a risk factor. There are two etiologically diverse subtypes of MCC: one due to clonal integration of the Merkel cell polyomavirus infection and the other due to the mutational effects of ultraviolet (UV