도서명: | Diagnostic Pathology: Familial Cancer Syndromes 2/e |
---|---|
정 가: | |
판매가: | 387,000원 |
적립금: | 11,610원 (3%) |
저 자: | Vania Nos |
출판사: | Elsevier |
ISBN : | 9780323712040 |
출판일: | 2020.02 |
판 형: | Hardcover |
수량: | |
판 수: | 2/e |
면 수: | 1000 page |
해외주문도서: | 해외 및 국내 입고 사정에 따라 2~4주 이상 소요될 수 있으며 - 해외주문은 취소 및 반품이 불가합니다. |
배송방법: | 택배 |
배송비: | 2,500원 (30,000원 이상 구매 시 무료) |
구매안내: | 네이버페이로 구매할 수 없는 상품입니다. |
배송주기
옵션선택 |
(최소주문수량 1개 이상 / 최대주문수량 0개 이하)
사이즈 가이드수량을 선택해주세요.
위 옵션선택 박스를 선택하시면 아래에 상품이 추가됩니다.
상품명 | 상품수 | 가격 |
---|---|---|
Diagnostic Pathology: Familial Cancer Syndromes 2/e | ( 11610) |
할인가가 적용된 최종 결제예정금액은 주문 시 확인할 수 있습니다.
의학서적전문 "성보의학서적"의 신간의학도서입니다.
This expert volume in the Diagnostic Pathology series is an excellent point-of-care resource for practitioners at all levels of experience and training. Physicians should have the knowledge derived from morphological findings to identify the likelihood of a cancer patient having an additional underlying familial syndrome— and to decide if that patient should undergo molecular genetic evaluation. This volume is specifically designed to help pathologists, oncologists, and other physicians who diagnose and treat cancer to recognize syndromes and syndrome- associated neoplasms and advise patients and their families on the possibility of a familial syndrome and their risk of developing other tumors. Diagnostic Pathology: Familial Cancer Syndromes, second edition, is an easy-to-use, one-stop reference for information on hereditary cancer syndromes, including differential diagnosis and management, that offers a templated, highly formatted design; concise, bulleted text; and superior color images throughout.
• Contains all the information necessary to determine whether a neoplasm typically encountered in daily practice is sporadic or related to a familial cancer syndrome
• Features a revised structure to keep you up to date: Part I includes more than 80 detailed chapters describing diagnoses associated with familial cancer syndromes; Part II contains more than 70 chapters with detailed descriptions of major syndromes (cross-referenced with diagnoses); and Part III features a molecular factors index that includes a complete description of each known gene associated with a familial cancer syndrome
• Contains updated chapters with newly classified GI, neurology, multiple organ, eye, endocrine, GYN, and kidney tumors, as well as more than 20 entirely new chapters covering recently recognized syndromes
• Incorporates up-to-date molecular findings and their significance for familial cancer syndromes; new techniques and technologies being used to discover gene mutations and other alterations; and details on personalized medicine targeted to specific genes
• Features more than 2,200 images throughout, including clinical and radiological images, algorithms, graphics, gross pathology, histology, and a wide range of special and immunohistochemical stains—all carefully annotated to highlight the most diagnostically significant factors
• Features time-saving bulleted text, key facts in each chapter, an extensive index, and numerous tables for quick reference and thorough understanding
• Includes the enhanced eBook version, which allows you to search all text, figures, and references on a variety of devices
-도서목차-
I. Diagnosis Associated With Syndromes by Organ
Breast
Breast Carcinoma, Female
Breast Carcinoma, Male
Breast Table
Blood and Bone Marrow
Acute Lymphoblastic Leukemia and Non-Hodgkin Lymphoma
Acute Myeloid Leukemia and Myelodysplastic Syndrome
Blood and Bone Marrow Table
Bone and Soft Tissue
Chondrosarcoma
Chordoma
Malignant Peripheral Nerve Sheath Tumor
Osteosarcoma
Rhabdomyosarcoma
Schwannoma
Bone and Soft Tissue Table
Head and Neck
Endolymphatic Sac Tumor
Squamous Cell Carcinoma
Head and Neck Table
Salivary Glands Table
Endocrine
Adrenal Cortex
Adrenal Cortical Adenoma
Adrenal Cortical Carcinoma
Adrenal Cortical Neoplasms in Children
Primary Pigmented Nodular Adrenocortical Disease
Adrenal Cortex Table
Adrenal Medulla and Paraganglia
Adrenal Medullary Hyperplasia
Neuroblastoma
Pheochromocytoma and Paraganglioma
Adrenal Medulla and Paraganglia Table
Pancreas
Pancreatic Neuroendocrine Neoplasms
Pancreas Table
Parathyroid
Parathyroid Adenoma
Parathyroid Carcinoma
Parathyroid Hyperplasia
Parathyroid Table
Pituitary
Pituitary Adenoma
Pituitary Hyperplasia
Pituitary Table
Thyroid, Medullary
C-Cell Hyperplasia
Medullary Thyroid Carcinoma
Thyroid, Medullary Table
Thyroid, Nonmedullary
Familial Thyroid Carcinoma
Follicular Thyroid Carcinoma
Thyroid, Nonmedullary Table
Gastrointestinal
Tubular Gut
Colon Adenoma
Esophageal Adenocarcinoma
Esophageal Squamous Cell Carcinoma
Gastric Adenocarcinoma
Gastrointestinal Stromal Tumor
Hamartomatous Polyps of GI Tract
Small Bowel Adenocarcinoma
Colon/Rectum Table
Esophagus/Stomach/Small Bowel Table
Tubular Gut Table
Hepatobiliary and Pancreas
Biliary Tract Neoplasia
Hepatoblastoma
Hepatocellular Carcinoma
Pancreatic Adenocarcinoma
Biliary Tract/Liver/Pancreas Table
Hepatobiliary and Pancreas Table
Genitourinary
Bladder
Bladder Table
Kidney
Angiomyolipoma
Clear Cell Renal Cell Carcinoma
HLRCC Syndrome-Associated Renal Cell Carcinoma
Papillary Renal Cell Carcinoma
Renal Oncocytoma, Chromophobe, and Hybrid Tumors
Wilms Tumor
Kidney Table
Prostate
Prostate Table
Renal Pelvis and Ureter
Renal Pelvis and Ureter Table
Testicle
Germ Cell Tumor
Sertoli Cell Neoplasms
Testicle Table
Gynecology
Cervical Tumors
Fallopian Tube Tumors
Ovarian Tumors
Uterine Tumors
Cervix
Endometrium
Fallopian Tube
Ovary
Nervous System
Central Nervous System
Eye
Peripheral Nervous System
Pulmonary
Adenocarcinoma, Lung
Adenocarcinoma With Lepidic (Bronchioloalveolar) Predominant Pattern
Lymphangioleiomyomatosis
Neuroendocrine Carcinoma, Lung
Pleuropulmonary Blastoma
Lung Table
Skin
BAP1-Inactivated Melanocytic Tumor
Basal Cell Carcinoma
Cutaneous Melanoma
Cutaneous Squamous Cell Carcinoma
Sebaceous Carcinoma
Skin Table
II. Overview of Syndromes
Introduction
Pathology of Familial Tumor Syndromes
Clinical Diagnosis and Management of Familial/Hereditary Tumor Syndromes
Molecular Aspects of Familial/Hereditary Tumor Syndromes
Syndromes
Ataxia Telangiectasia
BAP1 Tumor Predisposition Syndrome
Basal Cell Nevus Syndrome/Gorlin Syndrome
Beckwith-Wiedemann Syndrome
Birt-Hogg-Dubé Syndrome
Bloom Syndrome
Brooke-Spiegler Syndrome
Carney Complex
Costello Syndrome
Cystic Nephroma Syndrome
Denys-Drash Syndrome
Diamond-Blackfan Anemia
DICER1 Syndrome
Down Syndrome
Dyskeratosis Congenita
Familial Acute Myeloid Leukemia and Myelodysplastic Syndrome
Familial Adenomatous Polyposis
Familial Chordoma
Familial Gastrointestinal Stromal Tumor
Familial Infantile Myofibromatosis
Familial Isolated Hyperparathyroidism
Familial Medullary Thyroid Carcinoma
Familial Nonmedullary Thyroid Carcinoma
Familial Paraganglioma-Pheochromocytoma Syndrome
Familial Testicular Tumor
Familial Uveal Melanoma
Familial Wilms Tumor
Fanconi Anemia
GATA2 Spectrum Disorders
Glucagon Cell Hyperplasia and Neoplasia
Hereditary Breast/Ovarian Cancer Syndrome: BRCA1
Hereditary Breast/Ovarian Cancer Syndrome: BRCA2
Hereditary Diffuse Gastric Cancer
Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome (HLRCC)
Hereditary Multiple Exostosis
Hereditary Neuroblastoma
Hereditary Pancreatic Cancer Syndrome
Hereditary Papillary Renal Cell Carcinoma
Hereditary Paraganglioma/Pheochromocytoma Syndromes
Hereditary Prostate Cancer
Hereditary Renal Epithelial Tumors, Others
Hereditary Retinoblastoma
Hereditary SWI/SNF Complex Deficiency Syndromes
Heritable Gastrointestinal Stromal Tumors Syndromes
Howel-Evans Syndrome/Keratosis Palmares and Plantares With Esophageal Cancer
Hyperparathyroidism-Jaw Tumor Syndrome
Juvenile Polyposis Syndrome
Li-Fraumeni Syndrome/Li-Fraumeni-Like Syndrome
Lynch Syndrome
McCune-Albright Syndrome
Melanoma/Pancreatic Carcinoma Syndrome
Multiple Endocrine Neoplasia Type 1 (MEN1)
Multiple Endocrine Neoplasia Type 2 (MEN2)
Multiple Endocrine Neoplasia Type 4 (MEN4)
MYH-Associated Polyposis
Neurofibromatosis Type 1
Neurofibromatosis Type 2
Nijmegen Breakage Syndrome
Pancreatic Neuroendocrine Tumor Syndromes
*PDGFRA*-Mutant Syndrome
Peutz-Jeghers Syndrome
PTEN Hamartoma Tumor Syndromes
RASopathies: Noonan Syndrome
Rhabdoid Predisposition Syndrome
Schwannomatosis
Shwachman-Diamond Syndrome
Steatocystoma Multiplex
Succinate Dehydrogenase (SDH)-Deficient Renal Cell Carcinoma
Tuberous Sclerosis Complex
Tumor Syndromes Predisposing to Osteosarcoma
von Hippel-Lindau Syndrome
Werner Syndrome/Progeria
Wilms Tumor-Associated Syndrome
Wiskott-Aldrich Syndrome
Xeroderma Pigmentosum
Reference
Molecular Factors
Molecular Factors Index
기타 의학도서에 관련된 문의사항은 고객센터(02-854-2738) 또는 저희 성보의학서적 홈페이지내 도서문의 게시판에 문의바랍니다.
감사합니다.
성보의학서적 "http://www.medcore.kr
고객님께서 저희 성보의학서적에서 주문을 하신 주문번호가 생성이 되면 그에 따른 발송준비 및 배송절차는 다음과 같습니다
- 일반적으로 배송기간은 입금확인일로부터 3일 이내 배송을 원칙으로 합니다. 이는 재고가 확보된 도서의 경우입니다.
(단, 산간이나 지방 및 도서지역의 경우 약 1~2일이 더 소요될 수 있습니다.)
- 배송의 시점은 고객님의 주문 이후 입금확인 과정을 거쳐 배송이 됩니다.
- 주문도서의 배송 시 휴일이 포함된 경우는 24시간 순연됩니다.
- 배송료는 회원주문, 비회원주문 모두 2,500원 입니다. (일부 도서 및 산간지역은 추가 배송비 발생)
- 주문 금액이 30,000원 이상일 경우에는 무료로 배송해 드립니다.
- 반품/취소.환불 시 배송비는 무료로 배송이 되었을 경우, 처음 발생한 배송비까지 소급 적용될 수 있으며,
상품 하자로 인한 도서 교환시에는 무료로 가능합니다.
- 성보의학서적의 기본배송방법으로 택배서비스(한진택배&우체국)를 이용합니다.
해외원서의 경우
- 국내에서 재고를 보유한 업체가 없는 경우 해외주문을 해야 하는 상황이 생깁니다.
이 경우 4~5주 안에 공급이 가능하며 현지 출판사 사정에 따라 구입이 어려운 경우 2~3주 안에 공지해 드립니다.
- 재고 유무는 주문 전 사이트 상에서 배송 안내 문구로 구분 가능하며, 필요에 따라 전화 문의 주시면 거래처를 통해
다시 한번 국내재고를 확인해 드립니다.
- 해외 주문 도서는 고객님의 요청에 의해 주문하는 '개인주문' 상품으로, 단순한 고객변심/착오로 인한 취소, 교환, 반품은 불가능합니다.
- 해외주문 시 도서가격 및 수입 제반 비용 등을 모두 선결제로 진행하고 재고 관련 등의 사유로 취소, 교환, 반품이 불가능하오니
이점 꼭 숙지하시고 해외주문시 신중하게 주문하여 주시기 바랍니다.
반품안내
전자상거래에 의한 소비자보호에 관한 법률에 의거 반품 가능 기간내에는 반품을 요청하실 수 있습니다.
반품가능기간
- 단순변심 : 물품 수령 후 14일 이내 (단, 고객님의 요청으로 주문된 해외원서 제외)
- 주문하신 것과 다른 상품을 받으신 경우
- 파본인 상품을 받으신 경우- 개봉된 DVD, CD-ROM, 카세트테이프 (단, 배송 중 파손된 상품 제외)
- 탐독의 흔적이 있는 경우
- 소비자의 실수로 상품이 훼손된 경우
- 고객님의 주문으로 수입된 해외 도서인 경우
- 수령일로 14일 지난 상품의 경우
고객센터: (02)854-2738