標(biāo)題: Titlebook: Central Nervous System Tumors; Diagnostic Pathology César R. Lacruz Book 2023 The Editor(s) (if applicable) and The Author(s), under exclus [打印本頁] 作者: Malevolent 時(shí)間: 2025-3-21 17:59
書目名稱Central Nervous System Tumors影響因子(影響力)
書目名稱Central Nervous System Tumors影響因子(影響力)學(xué)科排名
書目名稱Central Nervous System Tumors網(wǎng)絡(luò)公開度
書目名稱Central Nervous System Tumors網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Central Nervous System Tumors被引頻次
書目名稱Central Nervous System Tumors被引頻次學(xué)科排名
書目名稱Central Nervous System Tumors年度引用
書目名稱Central Nervous System Tumors年度引用學(xué)科排名
書目名稱Central Nervous System Tumors讀者反饋
書目名稱Central Nervous System Tumors讀者反饋學(xué)科排名
作者: 無關(guān)緊要 時(shí)間: 2025-3-21 22:23
https://doi.org/10.1007/978-3-642-78906-9ther embryonal tumors, which include ., ., ., and .. In addition, . tumor has been introduced as a provisional entity within this category, whereas the broad designation . is included for embryonal tumors that defy a more specific diagnosis, e.g., that are . (diagnostic information necessary to assi作者: 失誤 時(shí)間: 2025-3-22 01:59 作者: Dungeon 時(shí)間: 2025-3-22 05:35 作者: 審問,審訊 時(shí)間: 2025-3-22 09:37 作者: Intruder 時(shí)間: 2025-3-22 16:42 作者: Intruder 時(shí)間: 2025-3-22 19:10 作者: dithiolethione 時(shí)間: 2025-3-22 21:55
logy, and immunohistochemical stains that support a morphologic discussion in which differential diagnosis and potential pitfalls are emphasized.?.Central Nervous System Tumors: Diagnostic Pathology. provides a978-3-031-51080-9978-3-031-51078-6作者: Venules 時(shí)間: 2025-3-23 04:03
https://doi.org/10.1007/978-3-031-51078-6Neuro-Oncology; Brain tumors advances; CNS Tumors; Diagnostic Pathology; Brain tumors; Brain Tumors Diagn作者: Compassionate 時(shí)間: 2025-3-23 09:12 作者: 召集 時(shí)間: 2025-3-23 13:43
Philip C. Bennett,William Caseycation—being necessary for the selection of the most appropriate therapy. CNS tumors, with their huge variety of types and subtypes (approximately 100 different primary brain tumors), each with its own clinical peculiarities and different cytohistologic characteristics, presented a great challenge f作者: Anticlimax 時(shí)間: 2025-3-23 15:17 作者: Coronation 時(shí)間: 2025-3-23 20:40 作者: amphibian 時(shí)間: 2025-3-24 01:16
R. Rüegsegger,B. Koller,B. Münchur primarily in children (age?
作者: mechanism 時(shí)間: 2025-3-24 03:20 作者: airborne 時(shí)間: 2025-3-24 07:18
Hanns-Martian Meyer,Karl Obermayr component is present in addition to this neuronal component. Both are rare neoplasms, which, taken as a whole, barely account for more than 3–4% of all primary intracranial tumors. However, because glioneuronal and neuronal tumors are the most common epilepsy-associated neoplasms, they are overrepr作者: 搖曳 時(shí)間: 2025-3-24 12:52
Masao Doi,James Harden,Takao Ohtaural evidence of ependymal differentiation. They account for 5% to 9% of all primary brain tumors in adults, 6% to 12% in children, and up to 30% in infants. Ependymal tumors are considered to originate from radial glial-like stem cells lining the wall of the ventricles or the wall of the spinal can作者: conquer 時(shí)間: 2025-3-24 18:05 作者: REP 時(shí)間: 2025-3-24 22:29 作者: LATHE 時(shí)間: 2025-3-25 00:42
Susanne Nowitzki-Grimm,Peter Grimmequency, these neoplasms often pose a diagnostic dilemma due to the diversity of pathologic types. Most pineal region neoplasms belong to the germ cell group, mainly . (over a half of pineal tumors) and ., followed by . (pineocytoma, pineal parenchymal tumor of intermediate differentiation, pineobla作者: Cupping 時(shí)間: 2025-3-25 06:49
https://doi.org/10.1007/978-3-642-78906-9ast majority of which are schwannomas. Craniospinal nerve sheath tumors may be encountered either sporadically or as a part of a variety of tumor predisposition syndromes, including neurofibromatosis type 1, neurofibromatosis type 2, schwannomatosis, and Carney complex. This chapter reviews the clin作者: Range-Of-Motion 時(shí)間: 2025-3-25 11:08 作者: 并入 時(shí)間: 2025-3-25 13:21
https://doi.org/10.1007/978-3-642-78906-9nting the homologous of neoplasms encountered far more frequently in the somatic soft tissues or bones. Thus, the 2021 WHO classification of CNS tumors has strived to align its terminology with their counterparts in the WHO Blue Book on Bone and Soft Tissue Tumors. Furthermore, three recently descri作者: 減至最低 時(shí)間: 2025-3-25 17:36
https://doi.org/10.1007/978-3-642-78906-9lanocytes. Lesions can manifest as diffuse disseminations within the subarachnoid space (meningeal melanocytosis and meningeal melanomatosis) or as solid masses (meningeal melanocytoma and meningeal melanoma). Meningeal melanocytomas with increased mitotic activity or invasion of the CNS parenchyma 作者: Derogate 時(shí)間: 2025-3-25 20:05 作者: Obloquy 時(shí)間: 2025-3-26 01:50
Harald Dyckhoff,Ulrich Derigs,Henk C. Tijmss. They represent a heterogeneous group of tumors composed primarily of histiocytes that are totally homologous to those of an extra-neuraxial location. Histiocytic tumors can be divided into two groups: Langerhans cell histiocytosis (LCH) and non-LCH (a group of disorders defined by the accumulatio作者: chastise 時(shí)間: 2025-3-26 06:42 作者: Formidable 時(shí)間: 2025-3-26 08:52
Werner Braun,Klaus P. Liesenfeldtructures converges. This is way this region can host such a numerous and heterogeneous group of neoplasms (Table .). This chapter will focus on updates for ., ., ., . (pituicytoma, granular cell tumor of the sellar region, spindle cell oncocytoma, sellar ependymoma), and . as well as discuss other 作者: Curmudgeon 時(shí)間: 2025-3-26 15:44
https://doi.org/10.1007/978-3-642-79192-5dults and about 2% in children. Recent advances in the management of patients with CNS metastases have made accurate diagnosis of these tumors of paramount importance. This chapter reviews the epidemiology; topography; clinicoradiologic features; diagnostic criteria—including ancillary studies—; and作者: Ardent 時(shí)間: 2025-3-26 18:57 作者: maculated 時(shí)間: 2025-3-27 00:24
Michael D. Lewan,Edward D. Pittmanpretation must be familiar with basic clinical and neuroimaging characteristics of known clinicopathologic entities. This chapter reviews these important topics and summarizes general interpretative guidelines.作者: tenuous 時(shí)間: 2025-3-27 01:18 作者: 代理人 時(shí)間: 2025-3-27 07:00
http://image.papertrans.cn/c/image/223199.jpg作者: 征兵 時(shí)間: 2025-3-27 09:30
Classification of the CNS Tumors,cation—being necessary for the selection of the most appropriate therapy. CNS tumors, with their huge variety of types and subtypes (approximately 100 different primary brain tumors), each with its own clinical peculiarities and different cytohistologic characteristics, presented a great challenge f作者: Vldl379 時(shí)間: 2025-3-27 14:06 作者: 幼稚 時(shí)間: 2025-3-27 20:12 作者: 遺留之物 時(shí)間: 2025-3-27 23:30
Pediatric-Type Diffuse Gliomas,ur primarily in children (age?
作者: vector 時(shí)間: 2025-3-28 02:09 作者: 防御 時(shí)間: 2025-3-28 09:35
Glioneuronal and Neuronal Tumors, component is present in addition to this neuronal component. Both are rare neoplasms, which, taken as a whole, barely account for more than 3–4% of all primary intracranial tumors. However, because glioneuronal and neuronal tumors are the most common epilepsy-associated neoplasms, they are overrepr作者: 傻 時(shí)間: 2025-3-28 12:33
Ependymal Tumors,ural evidence of ependymal differentiation. They account for 5% to 9% of all primary brain tumors in adults, 6% to 12% in children, and up to 30% in infants. Ependymal tumors are considered to originate from radial glial-like stem cells lining the wall of the ventricles or the wall of the spinal can作者: enchant 時(shí)間: 2025-3-28 15:31 作者: 包庇 時(shí)間: 2025-3-28 21:54 作者: 終端 時(shí)間: 2025-3-29 00:21
Pineal Tumors,equency, these neoplasms often pose a diagnostic dilemma due to the diversity of pathologic types. Most pineal region neoplasms belong to the germ cell group, mainly . (over a half of pineal tumors) and ., followed by . (pineocytoma, pineal parenchymal tumor of intermediate differentiation, pineobla作者: AMPLE 時(shí)間: 2025-3-29 06:00
Cranial and Paraspinal Nerve Tumors,ast majority of which are schwannomas. Craniospinal nerve sheath tumors may be encountered either sporadically or as a part of a variety of tumor predisposition syndromes, including neurofibromatosis type 1, neurofibromatosis type 2, schwannomatosis, and Carney complex. This chapter reviews the clin作者: COKE 時(shí)間: 2025-3-29 08:25 作者: 逗它小傻瓜 時(shí)間: 2025-3-29 14:20
Mesenchymal, Non-meningothelial Tumors,nting the homologous of neoplasms encountered far more frequently in the somatic soft tissues or bones. Thus, the 2021 WHO classification of CNS tumors has strived to align its terminology with their counterparts in the WHO Blue Book on Bone and Soft Tissue Tumors. Furthermore, three recently descri作者: 是剝皮 時(shí)間: 2025-3-29 15:42
Primary CNS Melanocytic Neoplasms,lanocytes. Lesions can manifest as diffuse disseminations within the subarachnoid space (meningeal melanocytosis and meningeal melanomatosis) or as solid masses (meningeal melanocytoma and meningeal melanoma). Meningeal melanocytomas with increased mitotic activity or invasion of the CNS parenchyma 作者: Misnomer 時(shí)間: 2025-3-29 21:52
Primary CNS Lymphomas,eal locations. Thus, by definition, there is no co-existing systemic disease at the time of diagnosis, distinguishing these lesions from CNS involvement arising from systemic .s (.s). The 2021?WHO classification scheme includes the entities listed in Table .. Despite impressive advances in the under作者: 邪惡的你 時(shí)間: 2025-3-30 02:29
Histiocytic Tumors of the CNS,s. They represent a heterogeneous group of tumors composed primarily of histiocytes that are totally homologous to those of an extra-neuraxial location. Histiocytic tumors can be divided into two groups: Langerhans cell histiocytosis (LCH) and non-LCH (a group of disorders defined by the accumulatio作者: 陰謀 時(shí)間: 2025-3-30 05:29
Germ Cell Tumors of the CNS,and have a marked predilection for males (more than twice as females). In the Europe and USA, the frequency is not high, representing approximately 0.5% of primary intracranial tumors and 3% of those affecting children. However, these figures are quadruple in eastern Asia (Taiwan, Japan, China, and 作者: 認(rèn)識 時(shí)間: 2025-3-30 09:34
Tumors of the Sellar Region,tructures converges. This is way this region can host such a numerous and heterogeneous group of neoplasms (Table .). This chapter will focus on updates for ., ., ., . (pituicytoma, granular cell tumor of the sellar region, spindle cell oncocytoma, sellar ependymoma), and . as well as discuss other 作者: 羊齒 時(shí)間: 2025-3-30 15:54
Metastases to the CNS and Its Coverings,dults and about 2% in children. Recent advances in the management of patients with CNS metastases have made accurate diagnosis of these tumors of paramount importance. This chapter reviews the epidemiology; topography; clinicoradiologic features; diagnostic criteria—including ancillary studies—; and作者: 舉止粗野的人 時(shí)間: 2025-3-30 17:43
Circumscribed Astrocytic Gliomas, is generally more favorable than the adult-type diffuse gliomas, being attempt of gross total resection the treatment of choice. This chapter reviews the clinicopathologic features and differential diagnosis of these entities as well as of their subtypes.作者: 生氣的邊緣 時(shí)間: 2025-3-30 20:54
Cranial and Paraspinal Nerve Tumors,icopathological features and differential diagnosis of schwannoma, neurofibroma, malignant melanotic nerve sheath tumor (previously melanotic schwannoma), malignant peripheral nerve sheath tumor, cauda equina neuroendocrine tumor (previously spinal paraganglioma), and ganglioneuroma.作者: barium-study 時(shí)間: 2025-3-31 04:42
Primary CNS Lymphomas,standing of the etiology and pathogenesis of primary CNS lymphomas, the mainstay of their diagnostic assessment remains tissue-based classification using histological and immunohistochemical analysis of biopsy specimens. This chapter reviews the clinicopathological features and differential diagnosis of all these entities.作者: 紡織品 時(shí)間: 2025-3-31 05:48 作者: Allergic 時(shí)間: 2025-3-31 09:50
Pineal Tumors,xclusively in this specific localization. This chapter will focus on updates for pineal parenchymal tumors; papillary tumor of the pineal region; desmoplastic myxoid tumor of the pineal region, SMARCB1-mutant; and pineal anlage tumor.作者: 極力證明 時(shí)間: 2025-3-31 15:43
3-D-Rekonstruktion bei Azetabulumfrakturenasic types: astrocytoma, IDH-mutant (CNS WHO grades 2, 3, 4); oligodendroglioma, IDH-mutant and 1p/19q-codeleted (CNS WHO grades 2, 3); and glioblastoma, IDH-wildtype (CNS WHO grade 4). This chapter reviews the clinicopathologic features and differential diagnosis of these entities as well as of their subtypes.作者: 擁護(hù)者 時(shí)間: 2025-3-31 21:16 作者: MOAT 時(shí)間: 2025-3-31 23:18 作者: aspect 時(shí)間: 2025-4-1 05:15 作者: 輕快走過 時(shí)間: 2025-4-1 06:28
https://doi.org/10.1007/978-3-642-78906-9atures and differential diagnosis of diffuse meningeal melanocytic tumors (melanocytosis and melanomatosis) and circumscribed meningeal melanocytic neoplasms (melanocytoma, melanoma, and intermediate-grade melanocytic neoplasm).作者: Mobile 時(shí)間: 2025-4-1 13:30 作者: 沒花的是打擾 時(shí)間: 2025-4-1 15:42 作者: 悠然 時(shí)間: 2025-4-1 22:22
Adult-Type Diffuse Gliomas,asic types: astrocytoma, IDH-mutant (CNS WHO grades 2, 3, 4); oligodendroglioma, IDH-mutant and 1p/19q-codeleted (CNS WHO grades 2, 3); and glioblastoma, IDH-wildtype (CNS WHO grade 4). This chapter reviews the clinicopathologic features and differential diagnosis of these entities as well as of their subtypes.作者: 殺人 時(shí)間: 2025-4-1 23:10
Pediatric-Type Diffuse Gliomas,classification requires molecular characterization and the integration of histopathological and molecular information (integrated diagnosis). This chapter reviews the clinicopathologic features and differential diagnosis of pediatric-type diffuse low-grade gliomas and pediatric-type diffuse high-grade gliomas作者: 眨眼 時(shí)間: 2025-4-2 05:47 作者: 哥哥噴涌而出 時(shí)間: 2025-4-2 10:25 作者: 傾聽 時(shí)間: 2025-4-2 11:44
Primary CNS Melanocytic Neoplasms,atures and differential diagnosis of diffuse meningeal melanocytic tumors (melanocytosis and melanomatosis) and circumscribed meningeal melanocytic neoplasms (melanocytoma, melanoma, and intermediate-grade melanocytic neoplasm).
