標(biāo)題: Titlebook: Atlas of Cutaneous Lymphomas; Classification and D Joi B. Carter,Amrita Goyal,Lyn McDivitt Duncan Book 2015 Springer International Publishi [打印本頁] 作者: 不讓做的事 時間: 2025-3-21 17:29
書目名稱Atlas of Cutaneous Lymphomas影響因子(影響力)
書目名稱Atlas of Cutaneous Lymphomas影響因子(影響力)學(xué)科排名
書目名稱Atlas of Cutaneous Lymphomas網(wǎng)絡(luò)公開度
書目名稱Atlas of Cutaneous Lymphomas網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Atlas of Cutaneous Lymphomas被引頻次
書目名稱Atlas of Cutaneous Lymphomas被引頻次學(xué)科排名
書目名稱Atlas of Cutaneous Lymphomas年度引用
書目名稱Atlas of Cutaneous Lymphomas年度引用學(xué)科排名
書目名稱Atlas of Cutaneous Lymphomas讀者反饋
書目名稱Atlas of Cutaneous Lymphomas讀者反饋學(xué)科排名
作者: Interstellar 時間: 2025-3-21 20:44 作者: HEAVY 時間: 2025-3-22 00:53
https://doi.org/10.1007/978-3-030-25237-3s condition is considered a provisional entity in the fourth edition of the WHO/EORTC guidelines [1]. This chapter will discuss the clinical presentation, prognosis, treatment, histopathology, immunophenotype, and differential diagnosis of pcGDTCL. It closes with two clinical cases, including clinical images and histopathology.作者: 開始從未 時間: 2025-3-22 08:31
Introduction to the T-Cell Lymphomas, 2]. The WHO/EORTC classification recognizes 15 cutaneous lymphomas, 10 of which are T-cell lymphomas. Their incidence and various organizational schemas for understanding CTCL are offered in this chapter. Each of the lymphomas is addressed individually in subsequent chapters.作者: LUDE 時間: 2025-3-22 09:58
Primary Cutaneous Gamma-Delta T-Cell Lymphoma,s condition is considered a provisional entity in the fourth edition of the WHO/EORTC guidelines [1]. This chapter will discuss the clinical presentation, prognosis, treatment, histopathology, immunophenotype, and differential diagnosis of pcGDTCL. It closes with two clinical cases, including clinical images and histopathology.作者: 憤憤不平 時間: 2025-3-22 13:58
Michael J. Urick,Vaughn Crandall, poikilodermatous MF, and hypopigmented MF. This chapter will discuss the clinical presentation, prognosis, treatment, histopathology, immunohistochemistry, and molecular biology of several of the subtypes of MF. It closes with five clinical cases, each representing a different subtype of MF.作者: 土產(chǎn) 時間: 2025-3-22 18:29 作者: 金絲雀 時間: 2025-3-22 23:36 作者: gain631 時間: 2025-3-23 05:06 作者: menopause 時間: 2025-3-23 06:16 作者: aggressor 時間: 2025-3-23 10:44
Lymphomatoid Papulosis,rimary cutaneous ALCL, and Hodgkin lymphoma, thus mandating careful surveillance of patients with LyP. This chapter addresses the clinical presentation, prognosis, and treatment of LyP, followed by a discussion of the immunohistochemical, histopathologic, and molecular characteristics of the four subtypes. It closes with a clinical case.作者: Pastry 時間: 2025-3-23 15:01 作者: 缺陷 時間: 2025-3-23 19:37 作者: Jingoism 時間: 2025-3-23 22:37 作者: 我還要背著他 時間: 2025-3-24 04:20 作者: ostensible 時間: 2025-3-24 10:27
Adult T-Cell Leukemia/Lymphoma,ATLL are highly varied and include erythroderma, purpuric papules, and plaques. This chapter addresses the clinical presentation, prognosis, treatment, histopathology, immunohistochemistry, and molecular characteristics of this disease. It closes with a differential diagnosis and clinical case.作者: Rebate 時間: 2025-3-24 12:58
Primary Cutaneous CD8+ Aggressive Epidermotropic Cytotoxic T-Cell Lymphoma,EORTC) classification guidelines. In this chapter we discuss the clinical presentation, prognosis, treatment, histopathology, immunohistochemistry, molecular characteristics, and differential diagnosis of CD8+ AECTCL. The chapter closes with a clinical case.作者: 侵略 時間: 2025-3-24 18:09
Primary Cutaneous Marginal Zone Lymphoma,is chapter will discuss the clinical presentation, prognosis, treatment, histopathology, immunophenotype, and differential diagnosis of pcMZL. It closes with a clinical case, including clinical images and histopathology.作者: Credence 時間: 2025-3-24 20:29
Book 2015first go-to text for those who are considering a diagnosis of cutaneous lymphoma in their differential diagnosis. The text also includes diagnostic mimics of lymphoma and differential diagnosis tables and algorithms. The target audience is general practitioners, dermatologists, pathologists and stud作者: membrane 時間: 2025-3-25 02:10
Michael B?hm,John H. Laragh,Manfred Zehendermas have revolutionized the clinical and histopathologic approaches to diagnosis and treatment of these highly varied diseases. This chapter outlines some aims of this book and offers a brief history of cutaneous lymphoma classification.作者: 粗語 時間: 2025-3-25 07:08
Intrapersonal and Interpersonal ARIA Processmmunity. Diagnosis is based on clinical presentation, flow cytometric analysis, and histopathology. This chapter discusses the clinical presentation, prognosis, treatment, histopathology, immunophenotype, and differential diagnosis of Sézary syndrome. It closes with two clinical cases, including clinical images, histopathology, and flow cytometry.作者: 說不出 時間: 2025-3-25 08:43
Jay Rothman,Donna Chrobot-MasonATLL are highly varied and include erythroderma, purpuric papules, and plaques. This chapter addresses the clinical presentation, prognosis, treatment, histopathology, immunohistochemistry, and molecular characteristics of this disease. It closes with a differential diagnosis and clinical case.作者: Omniscient 時間: 2025-3-25 12:20
Michael Fritsch,Michael WyrwichEORTC) classification guidelines. In this chapter we discuss the clinical presentation, prognosis, treatment, histopathology, immunohistochemistry, molecular characteristics, and differential diagnosis of CD8+ AECTCL. The chapter closes with a clinical case.作者: 創(chuàng)造性 時間: 2025-3-25 19:00
Allam Hamdan,Arezou Harraf,Hala Alsabatinis chapter will discuss the clinical presentation, prognosis, treatment, histopathology, immunophenotype, and differential diagnosis of pcMZL. It closes with a clinical case, including clinical images and histopathology.作者: ORE 時間: 2025-3-25 20:17
From Hypertension to Heart Failures of the cutaneous lymphomas, offer relevant clinical and histopathologic characteristics, and provide direction in navigating the often difficult task of distinguishing the various forms of cutaneous lymphoma.作者: 使迷惑 時間: 2025-3-26 01:43 作者: 繼而發(fā)生 時間: 2025-3-26 06:06
Sayda Ben Sghaier,Rafaa Mraihi,Arij Lahmarer lymphomas. This chapter addresses the clinical presentation, prognosis, treatment, histopathology, immunophenotype, and differential diagnosis of pcFCL. It closes with two clinical cases, including clinical images and histopathology.作者: 搜尋 時間: 2025-3-26 11:39 作者: 可以任性 時間: 2025-3-26 13:35 作者: 暫時休息 時間: 2025-3-26 20:05 作者: Tortuous 時間: 2025-3-26 22:32 作者: Overstate 時間: 2025-3-27 04:56
Intravascular Large B-Cell Lymphoma,ial origin; they are in fact derived from post–germinal center B cells [1, 2]. This chapter discusses the clinical presentation, prognosis, treatment, histopathology, immunohistochemistry, molecular characteristics, and differential diagnosis of iVLBCL. The chapter closes with two clinical cases featuring patients with ivLBCL.作者: insurrection 時間: 2025-3-27 08:25
Michael B?hm,John H. Laragh,Manfred Zehender unified classification scheme for lymphomas, including primary cutaneous lymphomas. Every year, new publications and workshops lead to a clearer understanding of the nuances of diagnosis and treatment of cutaneous lymphomas. Over the past 20 years, advances in the classification of cutaneous lympho作者: Inflammation 時間: 2025-3-27 10:16
From Hypertension to Heart Failureecular biology. The World Health Organization–European Organization for Research and Treatment of Cancer (WHO/EORTC) classification system recognizes 15 primary cutaneous lymphomas (Table 2.1). These lymphomas are divided into three overarching categories: T-cell lymphomas, B-cell lymphomas, and pre作者: penance 時間: 2025-3-27 15:04
https://doi.org/10.1007/978-3-642-54171-1t the ability to identify cell surface and intracellular markers and to assess if a population is clonal, it would be impossible to accurately diagnose most lymphomas. This chapter offers a brief introduction to the use of immunohistochemistry and other molecular techniques in diagnosing cutaneous l作者: Nuance 時間: 2025-3-27 20:10 作者: 障礙 時間: 2025-3-28 00:25 作者: 中止 時間: 2025-3-28 04:57 作者: multiply 時間: 2025-3-28 07:13
Jay Rothman,Donna Chrobot-MasonV-1). Patients with ATLL have an extremely poor prognosis, their disease complicated by multidrug resistance of malignant cells, infection due to impaired T-cell mediated immunity, hypercalcemia, and multiple organ failure. Half of patients develop cutaneous manifestations. The cutaneous lesions of 作者: 極大的痛苦 時間: 2025-3-28 12:44 作者: 出處 時間: 2025-3-28 16:24 作者: averse 時間: 2025-3-28 19:10
Developing Learning Organizations, This indolent lymphoma is the second most common of all cutaneous T-cell lymphomas. It typically presents with solitary cutaneous and subcutaneous erythematous-to-violaceous papules and nodules. Although relapse after treatment is very common, patients are typically asymptomatic, and the vast major作者: 地牢 時間: 2025-3-28 23:13 作者: 不透氣 時間: 2025-3-29 06:09 作者: 聚集 時間: 2025-3-29 08:44 作者: PURG 時間: 2025-3-29 11:41
The Rules of the Game Have Changed,provisional entity in the World Health Organization–European Organization for Research and Treatment of Cancer (WHO/EORTC) guidelines and is considered to have both indolent and aggressive forms. pcSMPTCL typically presents with a persistent, asymptomatic, solitary erythematous nodule or pink plaque作者: Hyaluronic-Acid 時間: 2025-3-29 18:21 作者: 倫理學(xué) 時間: 2025-3-29 20:21
Allam Hamdan,Arezou Harraf,Hala Alsabatinors. It has an excellent prognosis. This entity has also been known as cutaneous marginal zone lymphoma (CMZL), extranodal marginal zone lymphoma of mucosa associated lymphoid tissue (MZL or MALT lymphoma), primary cutaneous immunocytoma, primary cutaneous plasmacytoma, and lymphoma cutis [1, 2]. Th作者: –LOUS 時間: 2025-3-30 00:31
Sayda Ben Sghaier,Rafaa Mraihi,Arij Lahmarenter B cells constitutes 60 % of all primary cutaneous B-cell lymphomas and 9–11 % of all cutaneous lymphomas [1, 2]. It also includes 5 % of all follicular lymphomas, nodal and extranodal [3]. It typically presents with firm, erythematous to violaceous papules, plaques, and tumors on the scalp, tr作者: Axon895 時間: 2025-3-30 07:51
Quality Management System Audit,cally presents on the leg with erythematous or violaceous tumors or nodules, it can also present elsewhere on the body. Patients with pcDLBCL have a moderately poor prognosis and experience frequent systemic dissemination. Though small case series have reported dramatic improvements in survival with作者: 個阿姨勾引你 時間: 2025-3-30 09:42 作者: jovial 時間: 2025-3-30 15:33
Joi B. Carter,Amrita Goyal,Lyn McDivitt DuncanContains information on the latest lymphoma classification scheme and how to apply it.Highly illustrated with clinical and histopathological images of superb quality.Includes differential diagnosis an作者: Outspoken 時間: 2025-3-30 17:37
http://image.papertrans.cn/b/image/164149.jpg作者: explicit 時間: 2025-3-30 22:44 作者: 減弱不好 時間: 2025-3-31 01:00
Developing Learning Organizations, This indolent lymphoma is the second most common of all cutaneous T-cell lymphomas. It typically presents with solitary cutaneous and subcutaneous erythematous-to-violaceous papules and nodules. Although relapse after treatment is very common, patients are typically asymptomatic, and the vast majority do not experience extracutaneous spread.作者: 巨碩 時間: 2025-3-31 08:54
https://doi.org/10.1007/978-3-319-17217-0Cutaneous Lymphoma; Dermatology; Diagnostics; Histopathology; Oncology作者: Expand 時間: 2025-3-31 11:02 作者: persistence 時間: 2025-3-31 13:39
Immunohistochemistry and Molecular Techniques,t the ability to identify cell surface and intracellular markers and to assess if a population is clonal, it would be impossible to accurately diagnose most lymphomas. This chapter offers a brief introduction to the use of immunohistochemistry and other molecular techniques in diagnosing cutaneous lymphomas.作者: 進取心 時間: 2025-3-31 19:54
CD30+ Primary Cutaneous Anaplastic Large Cell Lymphoma, This indolent lymphoma is the second most common of all cutaneous T-cell lymphomas. It typically presents with solitary cutaneous and subcutaneous erythematous-to-violaceous papules and nodules. Although relapse after treatment is very common, patients are typically asymptomatic, and the vast majority do not experience extracutaneous spread.作者: Resection 時間: 2025-4-1 01:06
Introduction and a Brief History of Cutaneous Lymphoma Classification, unified classification scheme for lymphomas, including primary cutaneous lymphomas. Every year, new publications and workshops lead to a clearer understanding of the nuances of diagnosis and treatment of cutaneous lymphomas. Over the past 20 years, advances in the classification of cutaneous lympho作者: 標(biāo)準(zhǔn) 時間: 2025-4-1 02:12
Introduction to Cutaneous Lymphomas,ecular biology. The World Health Organization–European Organization for Research and Treatment of Cancer (WHO/EORTC) classification system recognizes 15 primary cutaneous lymphomas (Table 2.1). These lymphomas are divided into three overarching categories: T-cell lymphomas, B-cell lymphomas, and pre作者: 色情 時間: 2025-4-1 09:14
Immunohistochemistry and Molecular Techniques,t the ability to identify cell surface and intracellular markers and to assess if a population is clonal, it would be impossible to accurately diagnose most lymphomas. This chapter offers a brief introduction to the use of immunohistochemistry and other molecular techniques in diagnosing cutaneous l作者: 詞根詞綴法 時間: 2025-4-1 13:23
Introduction to the T-Cell Lymphomas,unctional, proliferative, and migratory capacities. The diversity of cutaneous T-cell lymphomas (CTCL) reflects the multiplicity of T-cell subsets [1, 2]. The WHO/EORTC classification recognizes 15 cutaneous lymphomas, 10 of which are T-cell lymphomas. Their incidence and various organizational sche作者: Legion 時間: 2025-4-1 14:37
