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Multicentric Castleman’s disease. Symptoms, diagnostics and therapy


Authors: Zdeněk Adam 1;  Zdeněk Řehák 2;  Zuzana Adamová 3;  Renata Koukalová 2;  Luděk Pour 1;  Marta Krejčí 1;  Ivanna Boichuk 1;  Viera Sandecká 1;  Martin Krejčí 1;  Martin Štork 1;  Sabina Ševčíková 4;  Zdeněk Král 1
Authors place of work: Interní hematologická a onkologická klinika LF MU a FN Brno 1;  Oddělení nukleární medicíny Masarykův onkologický ústav Brno 2;  Chirurgické oddělení nemocnice Frýdek-Místek 3;  Ústav patologické fyziologie LF MU, Brno 4
Published in the journal: Vnitř Lék 2022; 68(1): 41-53
Category: Review Articles

Summary

Castleman disease (CD) describes a group of heterogeneous hematologic disorders with characteristic histopathological features. CD can present with unicentric (UCD) or multicentric (MCD) regions of lymph node enlargement. Some cases of MCD are caused by human herpesvirus-8 (HHV-8), whereas others are HHV-8–negative/idiopathic (iMCD). Treatment of iMCD is challenging, and outcomes can be poor. In this paper, we briefly report about symptoms of iMCD and about the International, evidence‑based consensus diagnostic criteria for HHV-8-negative/idiopathic multicentric Castleman disease and International evidence based consensus treatment guidelines for idiopathic multicentric Castleman disease.

Keywords:

Castleman disease – siltuximab


Zdroje

1. Munshi N, Mehra M. van de Velde H, Desai A et al. Use of a claims database to characterize and estimate the incidence rate for Castleman disease. Leuk Lymphoma 2015; 56(5):1252-1260.

2. Adam Z, Pour L, Krejčí M et al. Lokalizovaná (unicentrická) forma Castlemanovy nemoci. Klinické projevy, diagnostika a léčba dle mezinárodních doporučení z roku 2020. Vnitř Lék 2021;67(8):462–471.

3. Fajgenbaum DC, vanRhee F, Nabel ChS. HHV-8 negative idiopathic multicentric Castleman disease: novel insight into biology pathogenesis and therapy. Blood 2014;123 (19):2924-2933.

4. Bower M, Pria AD, Coyle C et al. Diagnostic criteria schemes for multicentric Castleman disease in 75 cases. J Acquir Immune Defic Syndr. 2014;65(2):e80–e82.

5. Jakubíková M, Piťha J, Latta J, et al. Myasthenia gravis, Castleman disease, pemphigus, and anti‑phospholipid syndrome Muscle and nerve. 2013;47(3):447-451.

6. Cibičková Ľ, Soukup T, Bradna P et al. Asociace revmatoidní artritidy a Castlemanovy choroby. Česká revmatologie. 2005;13(3):106-109.

7. Sun DP, Chen WM, Wang L et al. Clinical characteristics and immunological abnormalities of Castleman disease complicated with autoimmune diseases. J Cancer Res Clin Oncol. 2021;147(7):2107-2115.

8. El Karoui K, Vuiblet V, Dion D et al. Renal involvement in Castleman disease. Nephrol Dial Transplant 2011;26(2):599-609.

9. Sydor A, Madura M, Wagrowska‑Danilewicz M. Amyloid a amyloidosis and renal failure in a course of Castleman disease. Nephrology (Carlton). 2007;12(6):620-621.

10. Dispenzieri A, Armitage J O, Loes M J et al. The clinical spectrum of Castleman’s disease. Amer J Hematol 2012;87:997-1002.

11. Dispenzieri A, Fajgenbaum DC. Overview of Castleman disease. Blood. 2020;135(16):1353- 1364.

12.Dispenzieri A. POEMS syndrome: 2014 update on diagnosis, risk‑stratification, and management. Am J Hematol 2014;89(2):214-223.

13. Fajgenbaum DC, Rosenbach M, van Rhee F, et al. Eruptive cherry hemangiomatosis associated with multicentric Castleman disease: a case report and diagnostic clue. JAMA Dermatol. 2013 Feb;149(2):204-208.

14. Garcia T, Dafer R, Hocker S, Schneck M et al. Recurrent strokes in two patients with POEMS syndrome and Castleman’s disease. J Stroke Cerebrovasc, DiS. 2007;16(6):278-284.

15. Huang J, Wang L, Zhou W, Jin J. Hyaline vascular Castleman disease associated with POEMS syndrome and cerebral infarction. Ann Hematol 86(1):59-61.

16. Szalat R, Munshi NC. Diagnosis of Castleman Disease. Hematol Oncol Clin North Am. 2018;32(1):53-64. doi: 10.1016/j.hoc.2017. 09. 005.

17. Ferda J, Ferdová E, Záhlava J et al. Fever of unknown origin: a value of (18)F‑FDG‑PET/ CT with integrated full diagnostic isotropic CT imaging.European journal of radiology. 2010;73(3):518-525.

18. Koa B et al. Emerging role of 18 F‑FDG PET/CT in Castleman disease: a review Insights Imaging.2021;12:35.

19. Koukalová R, Selingerová I, Řehák Z. FDG‑PET/ CT v diagnostice a hodnocení léčebné odpovědi Castlemanovy choroby – retrospektivní studie 29 případů z jednoho centra. Klinická onkologie. 2021;34(2):120-127.

20. Fajgenbaum DC, Uldrick TS, Bagg A et al. International, evidence‑based consensus diagnostic criteria for HHV-8-negative/idiopathic multicentric Castleman disease. Blood 2017;129(12):1646-1657.

21. Cronin DM, Warnke RA. Castleman disease: an update on classification and the spectrum of associated lesions. Adv Anat Pathol. 2009;16:236-246.

22. Masaki Y, Nakajima A, Iwao H et al. Japanese variant of multicentric castleman’s disease associated with serositis and thrombocytopenia--a report of two cases: is TAFRO syndrome (Castleman- Kojima disease) a distinct clinicopathological entity? J Clin Exp Hematop 2013;53(1):79-85.

23. Kawabata H, Takai K, Kojima M et al. Castleman‑Kojima disease (TAFRO syndrome): a novel systemic inflammatory disease characterized by a constellation of symptoms, namely, thrombocytopenia, ascites (anasarca), microcytic anemia, myelofibrosis, renal dysfunction, and organomegaly: J Clin Exp Hematop 2013;53(1):57-61.

24. Inoue M, Ankou M, Hua J et al. Complete resolution of TAFRO syndrome (thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly) after immunosuppressive therapies using corticosteroids and cyclosporin A: a case report. J Clin Exp Hematop. 2013;53(1):95-99.

25. Tedesco S, Postacchini L, Manfredi L et al. Successful treatment of a Caucasian case of multifocal Castleman’s disease with TAFRO syndrome with pathophysiology targeted therapy- case report. Exp Hematol Oncol 2015;4(1):3-10.

26. Masaki Y, Kawabata H, Takai K et al. Proposed diagnostic criteria, disease severity classification and treatment stratedy for Tafro syndrom, 2015 version. Int. J. Hematol 2016;103:686-692.

27. Yu L, Shi M, Cai Q et al. A Novel Predictive Model for Idiopathic Multicentric Castleman Disease: The International Castleman Disease Consortium Study. Oncologist. 2020;25(11):963-973.

28. Fang X, Sun Z, Xu‑Monette ZY et al. Model for Idiopathic Multicentric Castleman Disease Supporting Treatment Decisions. Oncologist. 2021;26(1):4–6.

29. Wu D, Lim MS, Jaffe ES. Pathology of Castleman Disease. Hematol Oncol Clin North Am. 2018;32(1):37-52.

30. van Rhee F, Greenway A, Stone K. Treatment of Idiopathic Castleman Disease. Hematol Oncol Clin North Am. 2018;32(1):89–106. doi: 10.1016/j.hoc.2017. 09. 008.

31. Van Rhee F, Voorhees P, Dispenzieri A et al al. International evidence based consensus treatment guidelines for idiopahtic multicentric Castleman disease. Blood 2018;132 (20):2115-2124.

Další literatura u autora a na www.casopisvnitrnilekarstvi.cz

Štítky
Diabetology Endocrinology Internal medicine
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