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Książki na temat „Rare neoplasias”

Autor: Grafiati

Data publikacji: 2 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

New Jersey. Cancer Registry Program., ed. Cancer in New Jersey: Incidence & mortality rates by race & sex for total cancer & eleven major sites, 1986-1988. Cancer Registry Program, Data Applications Program, Division of Epidemiology, Environmental, and Occupational Health Services, New Jersey State Dept. of Health, 1993.

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2

New Zealand Health Information Service., ed. Cancer patient survival: Covering the period 1994 to 2003. New Zealand Health Information Service, Ministry of Health, 2006.

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3

McEvily, Harris Catherine, ed. The race is run one step at a time: My personal struggle --and everywoman's guide--to taking charge of breast cancer. Simon & Schuster, 1991.

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4

Howe, Holly L. Annual cancer incidence by cancer type, sex, and race Illinois, 1986-1993. Illinois Dept. of Public Health, Illinois State Cancer Registry, 1995.

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5

Brinker, Nancy. The race is run one step at a time: My personal struggle-- and everywoman's guide to taking charge of breast cancer. Simon and Schuster, 1990.

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6

Brinker, Nancy. The race is run one step at a time: Every woman's guide to taking charge of breast cancer & my personal story. Summit Pub. Group, 1995.

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7

Davies, Kevin. Breakthrough: The race to find the breast cancer gene. J. Wiley, 1996.

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8

K, Gospodarowicz M., and International Union against Cancer, eds. Prognostic factors in cancer. 2nd ed. Wiley-Liss, 2001.

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9

McLaughlin, John R. Cancer survival in Ontario. Ontario Cancer Treatment and Research Foundation, 1995.

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10

F, Berrino, International Agency for Research on Cancer., and European Commission, eds. Survival of cancer patients in Europe: The EUROCARE study. World Health Organization, International Agency for Research on Cancer, 1995.

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11

E, Chang Alfred, ed. Oncology: An evidence-based approach. Springer, 2006.

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12

1947-, Tajima Kazuo, and Sonoda Shunro, eds. Ethnoepidemiology of cancer. Japan Scientific Societies Press, 1996.

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13

A, Miller Barry, Kolonel Laurence N, Coyle Linda, and National Institutes of Health (U.S.), eds. Racial/ethnic patterns of cancer in the United States, 1988-1992. U.S. Dept. of Health and Human Services, National Institutes of Health, 1998.

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14

R, Sankaranarayanan, Black Roger J, Parkin D. M, and International Agency for Research on Cancer., eds. Cancer survival in developing countries. International Agency for Research on Cancer, 1998.

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15

Elizabeth, Hewitt Maria, Ganz Patricia, Institute of Medicine (U.S.), American Society of Clinical Oncology., and American Society of Clinical Oncology and Institute of Medicine Symposium on Cancer Survivorship (November 2005 : Washington, DC), eds. From cancer patient to cancer survivor: Lost in transition. National Academies Press, 2006.

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16

Zahra, Sarafraz, Musavi Seyyed Ali, and Azaraein Mohammad Hossein. Rare Parotid Gland Neoplasms. LAP Lambert Academic Publishing, 2015.

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17

Beattie, R. Mark, Anil Dhawan, and John W.L. Puntis. Liver tumours. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569862.003.0060.

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Infantile haemangiomata 440Mesenchymal hamartoma 441Focal nodular hyperplasia (FNH) 441Nodular regenerative hyperplasia (NRH) 441Hepatoblastoma 442Hepatocellular carcinoma (HCC) 442Inflammatory pseudotumour 443Fibropolycystic liver disease 443Liver tumours in children are rare, accounting for 0.5–2% of all neoplasms in the paediatric age group....

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18

Ansell, Stephen M., and Various. Rare Hematological Malignancies. Springer, 2010.

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19

Ansell, Stephen M. Rare Hematological Malignancies. Springer, 2008.

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20

Rare tumors in children and adolescents. Springer, 2012.

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21

Rare tumors in children and adolescents. American society of nephrology, 2022.

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22

Ferrari, Andrea, Dominik T. Schneider, Ines B. Brecht, and Thomas A. Olson. Rare Tumors in Children and Adolescents. Springer International Publishing AG, 2022.

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23

Rare Tumors in Children and Adolescents. Springer International Publishing AG, 2023.

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24

Frisch, Morten. Penile Cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0055.

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Penile cancers are rare primary malignancies located on the glans, foreskin, or shaft of the penis, excluding the urethra. The vast majority of penile cancers are epithelial tumors representing histological subtypes of squamous cell carcinoma (SCC). Most penile SCCs are believed to develop through pre-invasive lesions known as penile intraepithelial neoplasia and penile carcinoma in situ. They account for 0.1%–0.3% of all incident cancers (excluding non-melanoma skin cancers) in the United States and other developed countries and up to 1% of all cancers in some countries in sub-Saharan Africa.

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25

Raghavan, Derek, David H. Johnson, Gregory H. Reaman, Charles D. Blanke, and Paul L. Moots. Textbook of Uncommon Cancer. Wiley & Sons, Incorporated, John, 2012.

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26

Brecher, Martin L., Neal J. Meropol, Derek Raghavan, David H. Johnson, and Paul L. Moots. Textbook of Uncommon Cancer. Wiley & Sons, Incorporated, John, 2006.

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27

Brecher, Martin L., Derek Raghavan, and David H. Johnson. Textbook of Uncommon Cancer. Wiley & Sons, Incorporated, John, 2006.

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28

Raghavan, Derek, Charles D. Blanke, Manmeet S. Ahluwalia, Jubilee Brown, and Edward S. Kim. Textbook of Uncommon Cancer. Wiley & Sons, Limited, John, 2017.

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29

Blanke, Charles, Derek Raghavan, David H. Johnson, Gregory H. Reaman, and Paul L. Moots. Textbook of Uncommon Cancer. Wiley & Sons, Incorporated, John, 2012.

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30

Raghavan, Derek, Charles D. Blanke, Manmeet S. Ahluwalia, Jubilee Brown, and Edward S. Kim. Textbook of Uncommon Cancer. Wiley & Sons, Limited, John, 2017.

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31

Beltran, Ralph J. Pheochromocytoma. Edited by Kirk Lalwani, Ira Todd Cohen, Ellen Y. Choi, and Vidya T. Raman. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190685157.003.0044.

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Pheochromocytoma is a rare type of neoplasm diagnosed in children. It originates in the adrenal gland and is different from paragangliomas which arise outside the adrenals. Both types of tumors arise from neural crest cells and lead to signs and symptoms related to hypersecretion of catecholamines. Related symptoms include hypertension, tachycardia, episodic headache, sweating, and abdominal pain. These tumors may be associated with multiple endocrine type 2 syndrome, multiple endocrine neoplasia, and von Hippel-Lindau disease, among other hereditary conditions. Pheochromocytomas can be malign

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32

Brady, Luther W., Luc Baert, and Zbigniew Petrovich. Carcinoma of the Kidney and Testis, and Rare Urologic Malignancies: Innovations in Management. Springer London, Limited, 2013.

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33

Petrovich, Zbigniew. Carcinoma of the Kidney and Testis, and Rare Urologic Malignancies: Innovations in Management. Brand: Springer, 2011.

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34

(Editor), Zbigniew Petrovich, L. Baert (Editor), and Luther W. Brady (Editor), eds. Carcinoma of the Kidney and Testis, and Rare Urologic Malignancies: Innovations in Management (Medical Radiology). Springer-Verlag Telos, 1999.

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35

Pagnoux, Christian, and Richard H. Swartz. Vasculitis of the Central Nervous System. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0099.

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Central nervous system (CNS) vasculitis is an extremely challenging diagnostic and therapeutic disease. Multiple conditions, including reversible cerebral vasoconstrictive syndrome and intracranial atherosclerosis, can mimic it. Infections, systemic diseases, particularly systemic vasculitides, drug abuse, neoplasms, and some other disorders can cause secondary CNS vasculitis. Primary CNS vasculitis is extremely rare. A definite diagnosis requires a brain biopsy, which may show granulomatous inflammation, lymphocytic inflammation, and/or acute necrotizing vasculitis. The pathogeny remains unkn

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36

Mirabello, Lisa, Rochelle E. Curtis, and Sharon A. Savage. Bone Cancers. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0042.

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Cancers arising from bone or cartilage account for about 0.2% of malignant neoplasms. They are histologically heterogeneous with multiple rare subtypes. Osteosarcoma and Ewing sarcoma occur primarily in children and young adults, whereas other bone cancers occur in older individuals. As a group, bone cancers have few known environmental risk factors, the exception being a strong association between therapeutic radiation and increased risk of osteosarcoma. The genetic etiology is also better understood in osteosarcoma, although there have been limited studies in other types of bone cancers. Thi

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37

Santos, Maria, Eric Bouffet, Carolyn Freeman, and Mark M. Souweidane. Choroid plexus tumours. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0006.

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Choroid plexus tumours are rare, intraventricular, primary central nervous system tumours derived from the choroid plexus epithelium. They occur predominantly in children and are classified based on histological criteria as choroid plexus papilloma, atypical choroid plexus papilloma, and choroid plexus carcinoma. Choroid plexus carcinomas can occur in the context of Li–Fraumeni syndrome, where the TP53 germline mutation predisposes patients to a wide range of neoplasms. Treatment of these tumours is challenging, due to their high vascularity and the young age of the patients. While surgery is

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38

Glockner, James F., Kazuhiro Kitajima, and Akira Kawashima. Magnetic resonance imaging. Edited by Christopher G. Winearls. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0015_update_001.

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Magnetic resonance imaging (MRI) provides excellent anatomic detail and soft tissue contrast for the evaluation of patients with renal disease. MRI needs longer scan time than computed tomography (CT); however, no radiation is involved. Gadolinium-based contrast agents (GBCAs) are used to help provide additional image contrast during MRI. MRI is indicated for characterization of renal mass, staging of malignant renal neoplasms, and determination of vena cava involvement by the renal tumour. Magnetic resonance (MR) angiography is widely accepted as a non-invasive imaging work-up of renal artery

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39

Prognostic Factors in Cancer, 2nd Edition. 2nd ed. Wiley-Liss, 2001.

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40

Neary, John, and Neil Turner. The patient with haematuria. Edited by Neil Turner. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0046.

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Haematuria is a common presenting feature of diseases of the kidney or the renal tract. It is also common in screening tests, single dipstick tests being positive in perhaps 5% of individuals. Age and whether the blood is visible (macroscopic) or non-visible (microscopic) impact largely on whether the explanation is likely to be broadly urological or nephrological. Origins are most commonly simple or urological. Macroscopic bleeding is rare in renal disease, and urine colour is then usually more rather smoky than red except when there is very acute inflammation. The chief urological causes are

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41

Cerhan, James R., Claire M. Vajdic, and John J. Spinelli. The Non-Hodgkin Lymphomas. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190238667.003.0040.

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The non-Hodgkin lymphomas (NHL) are a heterogeneous group of over forty lymphoid neoplasms that have undergone a major redefinition over the last twenty-five years, in part due to advances in immunology and genetics as well as implementation of the WHO classification system. NHLs are considered clonal tumors of B-cells, T-cells, or natural killer (NK) cells arrested at various stages of differentiation, regardless of whether they present in the blood (lymphoid leukemia) or lymphoid tissues (lymphoma). In the United States, the age-standardized NHL incidence rate (per 100,000) doubled from 1973

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42

Heidenreich, Axel. Testis cancer. Edited by James W. F. Catto. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199659579.003.0092.

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Testicular germ cell tumours represent the most common solid neoplasms in the age group of 20 to 40 years. These cancers have an excellent prognosis, with a 90% long-term survival rate due to well-established, interdisciplinary guidelines for diagnosis and treatment. Independent on the clinical stage at time of diagnosis, treatment after orchidectomy is performed on an individual risk adapted approach. In clinical stage I seminoma, active surveillance is the recommended therapy and adjuvant chemotherapy with carboplatin remains an option in men not suitable for surveillance. Clinical stage IIA

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43

Hutter, Robert V. P., Paul Hermanek, Leslie H. Sobin, Donald E. Henson, and Mary K. Gospodarowicz. Prognostic Factors in Cancer. Springer London, Limited, 2012.

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44

Ganz, Patricia A., Harvey I. Pass, Daniel F. Hayes, Alfred E. Chang, and Timothy Kinsella. Oncology: An Evidence-Based Approach. Springer London, Limited, 2007.

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45

(Editor), Alfred E. Chang, Patricia A. Ganz (Editor), Daniel F. Hayes (Editor), et al., eds. Oncology: An Evidence-Based Approach. Springer, 2005.

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46

Disrupting Breast Cancer Narratives: Stories of Rage and Repair. University of Toronto Press, Scholarly Publishing Division, 2019.

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47

(Editor), Suketami Tominaga, Tadao Kakizoe (Editor), and Shaw Watanabe (Editor), eds. Cancer Treatment and Survival Site-Specific Registries in Japan (Gann Monograph on Cancer Research). CRC, 1995.

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48

Wheelwright, Jeff. Wandering Gene and the Indian Princess: Race, Religion, and DNA. Norton & Company, Incorporated, W. W., 2012.

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49

The Wandering Gene and the Indian Princess: Race, Religion, and DNA. W. W. Norton, 2012.

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50

Cairns, John. Matters of Life and Death: Perspectives on Public Health, Molecular Biology, Cancer, and the Prospects for the Human Race. Princeton University Press, 2021.

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