The ultrastructure of the X organ sinus gland complex in sexually immature Chinese mitten crab Eriocheir sinensis was examined under the electron microscope. The sinus gland (SG) is composed primarily of nerve te...The ultrastructure of the X organ sinus gland complex in sexually immature Chinese mitten crab Eriocheir sinensis was examined under the electron microscope. The sinus gland (SG) is composed primarily of nerve terminals and glial cells. The terminal contains a great number of membrane bound granules, mitochondria, rough endoplasmic reticulum and electron lucent vesicles. The profiles of the terminals are sometimes exhibited finger like projections. The X organ (XO) locates at the ventral surface of the medulla terminalis ganglion in the eyestalk, oppositing to SG. According to the features of granule size, shape, electron density and cytoplasm, 6 types of terminals in SG and 7 types of neurosecretory (NS) cells in XO were identified. The release process by exocytosis of the granules in SG was observed and a tentative comparison was made for the granules between different types of terminals and NS cells. It seemed that they had a good correspondence since no change in electron density and just a slight increase of sizes was shown.展开更多
Small cell neuroendocrine carcinoma of the ampulla of Vater is extremely rare and different from the common ampullary adenocarcinoma. The ampullary adenoma is also a rare neoplasm and has the potential to develop an a...Small cell neuroendocrine carcinoma of the ampulla of Vater is extremely rare and different from the common ampullary adenocarcinoma. The ampullary adenoma is also a rare neoplasm and has the potential to develop an adenocarcinoma. Their coexistence has been rarely reported in the literature. We herein describe an unusual case of a small cell neuroendocrine carcinoma associated with a villous adenoma in the ampulla of Vater with emphasis on computed tomography (CT) and histopathological findings. We also discuss their clinical, histopathological and radiological features as well as possible histogenesis.展开更多
Objective To evaluate the effectiveness of three-dimensional computed tomography （3D-CT） guided radiofi＇equency trigeminal rhizotomy （RF-TR） in treatment of idiopathic trigeminal neuralgia （1TN）. Methods From ...Objective To evaluate the effectiveness of three-dimensional computed tomography （3D-CT） guided radiofi＇equency trigeminal rhizotomy （RF-TR） in treatment of idiopathic trigeminal neuralgia （1TN）. Methods From 1999 to 2001, 18 patients with ITN were treated with percutaneous controlled RF-TR. Intraoperative 3D-CT scanning was performed to guide the trajectory of the puncture. After correction of the needle tip according to the CT scans and stimulation effects, 2 to 5 lesions were made for a duration of 60-90 seconds at a temperature of 60℃ to 75℃ depending on the pain distribution and the age of patient. The needles located in foramen ovale. Pain alleviated immediately with no serious complication in all patients. The patients were followed up for an average of 31.5 months （range 24-41 months）. Acute pain relief was experienced by 17 patients after the procedure, reaching an initial success rate of 94.4%. Early （〈 6 months） pain recurrence was observed in 2 patients （11.1%）, whereas late （〉 6 months） recurrence was reported in 3 patients （16.7%）. Thirteen patients had complete pain control, with no need for medication thereafter. Five cases experienced partial pain relief, but required medication at a lower dose than in the preoperative period. Conclusion 3D-CT foramen ovale locations can raise the successful rate of puncture, enhance the safety, and reduce the incidence rate of complication.展开更多
Fragile X syndrome （FXS） is the most common form of inherited mental retardation, characterized by moderate-to- severe mental retardation, attention deficits, and hyperactivity. This disease results from the expansi...Fragile X syndrome （FXS） is the most common form of inherited mental retardation, characterized by moderate-to- severe mental retardation, attention deficits, and hyperactivity. This disease results from the expansion of a trinucleotide repeat （CGG） within the X-linked fragile X mental retardation l （FMR1） gene, which leads to the lack of the product of the FMR1 gene--fragile X mental retardation protein. Many mental disorders such as FXS and Rett syndrome are thought to originate during early developmental period, but recent findings have suggested the involvement of the processes in the adult nervous system. Here we outline our recent studies and initial clinical trials that may provide an approach to treat FXS in the adulthood.展开更多
文摘The ultrastructure of the X organ sinus gland complex in sexually immature Chinese mitten crab Eriocheir sinensis was examined under the electron microscope. The sinus gland (SG) is composed primarily of nerve terminals and glial cells. The terminal contains a great number of membrane bound granules, mitochondria, rough endoplasmic reticulum and electron lucent vesicles. The profiles of the terminals are sometimes exhibited finger like projections. The X organ (XO) locates at the ventral surface of the medulla terminalis ganglion in the eyestalk, oppositing to SG. According to the features of granule size, shape, electron density and cytoplasm, 6 types of terminals in SG and 7 types of neurosecretory (NS) cells in XO were identified. The release process by exocytosis of the granules in SG was observed and a tentative comparison was made for the granules between different types of terminals and NS cells. It seemed that they had a good correspondence since no change in electron density and just a slight increase of sizes was shown.
文摘Small cell neuroendocrine carcinoma of the ampulla of Vater is extremely rare and different from the common ampullary adenocarcinoma. The ampullary adenoma is also a rare neoplasm and has the potential to develop an adenocarcinoma. Their coexistence has been rarely reported in the literature. We herein describe an unusual case of a small cell neuroendocrine carcinoma associated with a villous adenoma in the ampulla of Vater with emphasis on computed tomography (CT) and histopathological findings. We also discuss their clinical, histopathological and radiological features as well as possible histogenesis.
文摘Objective To evaluate the effectiveness of three-dimensional computed tomography （3D-CT） guided radiofi＇equency trigeminal rhizotomy （RF-TR） in treatment of idiopathic trigeminal neuralgia （1TN）. Methods From 1999 to 2001, 18 patients with ITN were treated with percutaneous controlled RF-TR. Intraoperative 3D-CT scanning was performed to guide the trajectory of the puncture. After correction of the needle tip according to the CT scans and stimulation effects, 2 to 5 lesions were made for a duration of 60-90 seconds at a temperature of 60℃ to 75℃ depending on the pain distribution and the age of patient. The needles located in foramen ovale. Pain alleviated immediately with no serious complication in all patients. The patients were followed up for an average of 31.5 months （range 24-41 months）. Acute pain relief was experienced by 17 patients after the procedure, reaching an initial success rate of 94.4%. Early （〈 6 months） pain recurrence was observed in 2 patients （11.1%）, whereas late （〉 6 months） recurrence was reported in 3 patients （16.7%）. Thirteen patients had complete pain control, with no need for medication thereafter. Five cases experienced partial pain relief, but required medication at a lower dose than in the preoperative period. Conclusion 3D-CT foramen ovale locations can raise the successful rate of puncture, enhance the safety, and reduce the incidence rate of complication.
基金supported by the National Natural Science Foundation of China (No. 30670684,30770686)
文摘Fragile X syndrome （FXS） is the most common form of inherited mental retardation, characterized by moderate-to- severe mental retardation, attention deficits, and hyperactivity. This disease results from the expansion of a trinucleotide repeat （CGG） within the X-linked fragile X mental retardation l （FMR1） gene, which leads to the lack of the product of the FMR1 gene--fragile X mental retardation protein. Many mental disorders such as FXS and Rett syndrome are thought to originate during early developmental period, but recent findings have suggested the involvement of the processes in the adult nervous system. Here we outline our recent studies and initial clinical trials that may provide an approach to treat FXS in the adulthood.
