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Books on the topic 'Sarcoidoses'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

G, Scadding J., ed. Sarcoidosis. London: Hodder Arnold, 2012.

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2

N, Mitchell D., ed. Sarcoidosis. 2nd ed. London: Chapman & Hall, 1985.

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3

Scadding, J. G., and D. N. Mitchell. Sarcoidosis. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-2971-6.

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4

Judson, Marc A., ed. Pulmonary Sarcoidosis. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-8927-6.

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5

Freeman, Andrew M., and Howard D. Weinberger, eds. Cardiac Sarcoidosis. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-14624-9.

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6

Nagata, Alfrieda. Understanding sarcoidosis. [Bethesda, Md.?]: Clinical Center Communications, National Institutes of Health, 1988.

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7

Jones, Williams W., ed. Sarcoidosis and other granulomatous disorders. Philadelphia: Saunders, 1985.

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8

Connor, Michael R., and Ryan S. Stevens. Sarcoidosis: Diagnosis, epidemiology, and treatment options. Hauppauge, N.Y: Nova Science Publishers, 2011.

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9

Parker, James N., and Philip M. Parker. The official patient's sourcebook on sarcoidosis. Edited by Icon Group International Inc. San Diego, Calif: Icon Health Publications, 2002.

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10

P, Sharma Om, ed. Atlas of sarcoidosis: Pathogenesis, diagnosis, and clinical features. New York: Springer, 2005.

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11

1926-, Grassi Carlo, Rizzato Gianfranco, and Pozzi Ernesto, eds. Sarcoidosis and other granulomatous disorders: Proceedings of the XI World Congress on Sarcoidosis and Other Granulomatous Disorders, Milan, 6-11 September 1987. Amsterdam: Excerpta Medica, 1988.

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12

Sarcoidosis: Resource guide and directory : a medical mystery uncovered, facts, information, and helplines. Piscataway, N.J: PC Publications, 1991.

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13

International, Conference on Sarcoidosis and Other Granulomatous Disorders (10th 1984 Baltimore Md ). Tenth International Conference on Sarcoidosis and Other granulomatous disorders. New York, N.Y: New York Academy of Sciences, 1986.

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14

K, Sarcoidosis Association U. Sarcoidosis: A guide to the literature for medical practitioners and librarians. [St Helens] (19, Ashurst Close, St Helens, Lancashire WA11 9DN): The Association, 1990.

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15

Moonlight sonata at the Mayo Clinic. Detroit: Thorndike Press,A part of Gale, Cengage Learning, 2013.

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16

Gallagher, Nora. Moonlight sonata at the Mayo Clinic. New York: Alfred A. Knopf, 2013.

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17

Model patient: My life as an incurable wise-ass. New York, NY: Perennial, 2001.

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18

Duffy, Karen. Model Patient. New York: HarperCollins, 2007.

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19

Duffy, Karen. Model patient: My life as an incurable wise-ass. New York, NY: Cliff Street Books, 2000.

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20

Parker, James N., and Philip M. Parker. Sarcoidosis: A medical dictionary, bibliography and annotated research guide to Internet references. San Diego, CA: ICON Health Publications, 2004.

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21

Transformed one winter. Nashville, Tenn: Broadman Press, 1989.

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22

Hashefi, Mandana. PET/CT applications in non-neoplastic conditions. Edited by New York Academy of Sciences. Boston, Mass: Published by Blackwell Pub. on behalf of the New York Academy of Sciences, 2011.

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23

Panniculitis. Philadelphia, Pa: Saunders, 2008.

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24

National Heart, Lung, andlood Institute, ed. Sarcoidosis. [Bethesda, Md.]: U.S. Dept. of Health and Human Services, [National Institutes of Health, National Heart, Lung, and Blood Institute?, 2003.

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25

Jack, Lieberman, ed. Sarcoidosis. Orlando: Grune & Stratton, 1985.

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26

Eishi, Yoshinobu, ed. Sarcoidosis. InTech, 2013. http://dx.doi.org/10.5772/45958.

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27

Müller-Quernheim, Joachim, Gernot Zissel, and Antje Prasse. Sarcoidosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0167.

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Abstract:

Sarcoidosis is a systemic disease characterized by non-necrotizing granulomata and manifestations in almost any organ. Diagnosis relies on the exclusion of other granulomatous disorders and a compatible pattern of symptoms and clinical findings. Inflammatory lesions and granulomata may undergo spontaneous resolution or persist in chronic disease with eventual fibrosis and permanent organ damage. Immunological disease mechanisms are linked to severe derangements of the cytokine network. In systemic resolution or under prednisolone therapy of symptomatic disease proinflammatory cytokines are downregulated and histological lesions may completely vanish. Corticosteroid-resistant disease, however, requires treatment with an immunosuppressive regimen consisting of prednisolone and an immunosuppressive agent or anti-tumour necrosis factor (TNF) monoclonal antibodies.

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28

Drent, M., and U. Costabel, eds. Sarcoidosis. European Respiratory Society, 2005. http://dx.doi.org/10.1183/1025448x.erm3205.

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29

Sarcoidosis. Elsevier, 2019. http://dx.doi.org/10.1016/c2016-0-04561-8.

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30

P, Baughman Robert, ed. Sarcoidosis. New York: Taylor & Francis, 2005.

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31

P, Sharma Om, ed. Sarcoidosis. Philadelphia: Saunders, 1997.

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32

National Heart, Lung, and Blood Institute. Division of Lung Diseases and National Heart, Lung, and Blood Institute. Office of Prevention, Education, and Control, eds. Sarcoidosis. [Bethesda, Md.?]: U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, 1991.

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33

Mitchell, Donald, Athol Wells, Stephen Spiro, and David Moller, eds. Sarcoidosis. CRC Press, 2012. http://dx.doi.org/10.1201/b13322.

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34

Baughman, Robert, ed. Sarcoidosis. CRC Press, 2005. http://dx.doi.org/10.1201/b13773.

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35

Bloom, Chloe, and Seamus Donnelly. Pulmonary sarcoidosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199657742.003.0019.

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This case of a young female with suspected pulmonary sarcoidosis demonstrates the difficulties in confirming the diagnosis and subsequently identifying the appropriate treatment. Current guidelines were developed in the 1990s, and there has been little change in the diagnostic pathway since then. However, there are new clinical tools to help differentiate from the common differential diagnosis of tuberculosis. The patient’s management can be complex, with a host of clinical parameters that can be potentially used to assess each patient’s disease activity, severity, and prognosis, and the decision to start immunosuppressive treatment is often difficult. The mainstay of treatment remains glucocorticoids, with a wide choice of possible steroid-sparing agents. However, the evidence for their use is limited. This case is particularly interesting, as the patient is a female with a young daughter who is planning imminently on continuing her family and has legitimate concerns about treatment side effects.

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36

Atlas of Sarcoidosis. London: Springer-Verlag, 2005. http://dx.doi.org/10.1007/b138736.

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37

(Editor), J. Costabel, and M. Drent (Editor), eds. Sarcoidosis (European Respiratory Monograph). European Respiratory Society, 2005.

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38

Rajakariar, Ravindra, and Muhammad M. Yaqoob. The patient with sarcoidosis. Edited by Giuseppe Remuzzi. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0156.

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Renal involvement in sarcoidosis is common and often under-recognized. The most frequent manifestation is acute kidney injury secondary to hypercalcaemia and granulomatous tubulointerstitial nephritis. The latter can lead to both acute kidney injury and to slowly progressive chronic renal impairment with concomitant chronic damage seen on histology. This chapter describes the types of renal disease that may occur in sarcoidosis and the pathogenesis, clinical presentation, diagnosis, and treatment of the patient with sarcoidosis. Corticosteroid therapy is the cornerstone of therapy. In patients with granulomatous tubulointerstitial nephritis, the authors recommend long-term, low-dose maintenance steroids.

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39

Sharma, Om P., and Violeta Mihailovic-Vucinic. An Atlas of Sarcoidosis. Springer, 2005.

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40

Kalantar Motamedi, Mohammad Hosein, ed. Sarcoidosis Diagnosis and Management. InTech, 2011. http://dx.doi.org/10.5772/909.

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41

Baughman, Robert Phillip, and Dominique Valeyre. Sarcoidosis: A Clinician's Guide. Elsevier - Health Sciences Division, 2018.

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42

O'Donnell, Dearbhaile Máirí. A Study of immunoregulatory mechanisms in the T-Cell alveolitis of sarcoidosis. 1997.

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43

Harper, Darren. Sarcoidosis: Clinical Manifestations, Diagnostic Methods and Management Strategies. Nova Science Publishers, Incorporated, 2015.

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44

Judson, Marc A. Pulmonary Sarcoidosis: A Guide for the Practicing Clinician. Humana, 2013.

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45

Conroy, Sandra. Sarcoidosis Resource Guide and Directory. PC Pubns, 1992.

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46

Gerolemou, Louis. Basic Diagnostic Approaches in Sarcoidosis. INTECH Open Access Publisher, 2011.

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47

Geraint, James D., ed. Sarcoidosis and other granulomatous disorders. New York: M. Dekker, 1994.

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48

Sarcoidosis - New Perspectives [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.92488.

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49

Rivera, Frank. I Have Sarcoidosis but It Doesn't Have Me: My Fight and Advocacy with Sarcoidosis. Independently Published, 2020.

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50

Publications, ICON Health. The Official Patient's Sourcebook on Sarcoidosis. Icon Health Publications, 2002.

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