Kastlemanova bolest udružena sa mešanim poremećajem vezivnog tkiva i cerebralnom ishemijom i vaskulitisom: redak slučaj i dijagnostički izazov za infektologa

  • Lidija Popović Dragonjić Clinical Center Niš, Clinic for Infectious Diseases, Niš, Serbia
  • Maja Jovanović Clinical Center Niš, Clinic for Infectious Diseases, Niš, Serbia
  • Miodrag Vrbić Clinical Center Niš, Clinic for Infectious Diseases, Niš, Serbia
  • Maja Stanojević University of Belgrade, Department of Microbiology and Immunology, Belgrade, Serbia
  • Miljan Krstić University of Niš, Faculty of Medicine, Department of Pathology, Niš, Serbia
  • Aleksandar Tasić Clinical Center Niš, Center for Radiology, Niš, Serbia
  • Nikola Živković University of Niš, Faculty of Medicine, Department of Pathology, Niš, Serbia
Ključne reči: kastlemanova bolest, dijagnostičke tehnike i procedure, dijagnoza diferencijalna, neurološke manifestacije, histologija

Sažetak


Uvod. Kastlemanova bolest (KB) ili angiofolikularna hiperplazija limfnih čvorova je redak patohistološki proces koji se karakteriše ne-neoplastičnom reaktivnom proliferacijom limfnog tkiva. S obzirom da imitira kliničke i laboratorijske znake infekcije, može predstavljati značajan dijagnostički problem za infektologa. Prikaz bolesnika. Predstavljamo tok bolesti tridesetdevetogodišnjeg muškarca kod koga je u početku bila postavljena klinička sumnja na infekciju centralnog nervnog sistema (CNS), koja je najviše podsećala na neurotuberkulozu. Među ostalim mogućim dijagnozama našli su se i malignitet sa metastazama u kostima i limfom. U daljem toku, kod bolesnika je histološkom analizom limfnog čvora utvrđena KB, što je bilo presudno u odbacivanju sumnje na malignitet i tuberkulozu. Dodatnim analizama je kod bolesnika utvrđena mešovita bolest vezivnog tkiva (MBVT). Magnetnom rezonancom otkriven je vaskulitis mezencefalona i talamusa. Zaključak. Kastlemanova bolest sa zahvatanjem CNS-a veoma je retka, kao i KB udružena sa MBVT, što zajedno ovaj slučaj čini još jedinstvenijim. Ovim prikazom slučaja naglašava se važnost definitivne histološke dijagnoze kod bolesnika sa limfadenopatijom i pridruženim sistemskim manifestacijama i potreba za dodatnim imunološkim i radiološkim analizama.

Reference

Castleman B, Iverson L, Menendez VP. Localized mediastinal lymph-node hyperplasia resembling thymoma. Cancer 1956; 9(4): 822–30.

Roca B, Torres V. Castleman's disease presenting as fever of unknown origine: diagnostic value of fluorodeoxyglucose-positron emission tomography/computed tomography. Am J Med Sci 2009; 337(4): 295–6.

Fajgenbaum DC, van Rhee F, Nabel CS. HHV-8-negative, idio-pathic multicentric Castleman disease: novel insights into bi-ology, pathogenesis and therapy. Blood 2014; 123(19): 2924–33.

JK, Kim Y. Surgical Management of Unicentric Castleman's disease in the abdomen. Ann Coloproctol 2014; 30(2): 97-100.

Fajgenbaum DC, Uldrick TS, Bagg A, Frank D, Wu D, Srkalovic G, et al. International, evidence-based consensus diagnostic criteria for HHV-8-negative/idiopathic multicentric Cas-tleman disease. Blood 2017; 129(12): 1646–57.

Simpson D. Epidemiology of Castleman disease. Hematol On-col Clin North Am 2018; 32(1): 1–10.

Robinson D Jr, Reynolds M, Casper C, Dispenzieri A, Vermeulen J, Payne K, et al. Clinical epidemiology and treatment patterns of patients with multicentric Castleman disease: results from two US treatment centres. Br J Haematol 2014; 165(1): 39–48.

Maric N, Stanic V, Cvijanovic V, Ristanovic A, Kovacevic S, Krivokapic Z, et al. Surgical treatment of unicentric plasma cell histological type Castleman's disease. Vojnosanit Pregl 2011; 68(9): 795–9.

Muskardin TW, Peterson BA, Molitor JA. Castleman disease and associated autoimmune disease. Curr Opin Rheumatol 2012; 24(1): 76–83.

Hosaka S, Kondo H. Three cases of Castleman's disease mimick-ing the features of collagen disease. Ryumachi 1994; 34(1): 42–7.

Lokesh S, Tony K, Raghupathy VS, Malepati B. A Rare Case of Mixed Connective Tissue Disease (MCTD) with Intricate Fea-tures of Lupus, Polymyositis and Rheumatoid Arthritis Pre-senting with Severe Myositis. J Clin Diagn Res 2015; 9(3): OD05–7.

Dispenzieri A, Armitage JO, Loe MJ, Geyer SM, Allred J, Ca-moriano JK, et al. The clinical spectruma of Castleman’s dis-ease. Am J Hematol 2012; 87(11): 997–1102.

Cummings TJ, Gong JZ, Friedman AH, McLendon RE. Cas-tlemans Disease Confined to the Leptomeninges. Ann Clin Lab Sci 2000; 30(3): 278–82.

Matsumura K, Nakasu S, Tanaka T, Nioka H, Matsuda M. Intra-cranial localized Castleman’s disease – case report. Neurol Med Chir (Tokyo) 2005; 45(1): 59–65.

Yu H, Yao F, Li Y, Li J, Cui QC. Castleman disease variant of POEMS syndrome complicated with multiple cerebral infarc-tion: a rare case report and review of literature. Int J Clin Exp Pathol 2015; 8(10): 13578–83.

Chan KL, Lade S, Prince HM, Harrison SJ. Update and new ap-proaches in the treatment of Castleman disease. J Blood Med 2016; 7: 145–58.

Yu L, Tu M, Cortes J, Xu-Monette ZY, Miranda RN, Zhang J, et al. Clinical and pathological characteristics of HIV- and HHV-8-negative Castleman disease. Blood 2017; 129(12): 1658–68.

Mohtaram A, Afif M, Sghiri T, Rami A, Latib R, Kettani F, et al. Coexistence of Hodgkin’s Lymphoma and Castleman’s Dis-ease: A Case Report with Successful Response to Chemother-apy and Radiotherapy. Case Rep Oncol Med 2013; 2013: 487205.

Objavljeno
2021/04/08
Rubrika
Prikaz bolesnika