Partial Regression of CNS Lesions of Erdheim-Chester Disease after Treatment with 2-chlorodeoxadenosine and Their Full Remission Following Treatment with Lenalidomide
Authors:
Z. Adam 1; A. Šprláková 2; Z. Řehák 3; R. Koukalová 3; P. Szturz 1; M. Krejčí 1; L. Pour 1; L. Zahradová 1; L. Červinek 1; L. Křen 4; M. Moulis 1; M. Hermanová 5; M. Mechl 2; J. Prášek 6; R. Hájek 1; Z. Král 1; J. Mayer 1
Authors place of work:
Interní hematoonkologická klinika, LF MU a FN Brno
1; Radiologická klinika, LF MU a FN Brno
2; Oddělení PET CT, Masarykův onkologický ústav, Brno
3; Ústav patologie, LF MU a FN Brno
4; Ústav patologické anatomie, LF MU a FN Brno
5; Klinika nukleární medicíny, Brno
6
Published in the journal:
Klin Onkol 2011; 24(5): 367-381
Category:
Kazuistiky
Summary
Introduction:
Erdheim-Chester disease is a very rare syndrome affecting adult population. It typically causes hyperostosis of long bones, retroperitoneal fibrosis and widening of the aortic wall. Patients frequently suffer from disease-associated fevers and pain in the lower limbs. No guidelines are available for the treatment of this rare ailment. Therefore, we describe our experience with lenalidomide in a patient with poor treatment response to 2-chlorodeoxyadenosine.
Case:
Diabetes insipidus and neurological problems developing over 4 years were the first signs of the disease. The disease was diagnosed from histology of the bone marrow extracted from the ilium. At diagnosis, the patient had multiple infiltrates in the brain, widened wall of the thoracic and abdominal aorta, fibrotic changes to retroperitoneum and typical hyperostosis of the long bones of lower limbs with high accumulation of technetium pyrophosphate as well as fluorodeoxyglucose. First line treatment involved 2-chlorodeoxyadenosine 5 mg/m2 s.c. for 5 consecutive days every 28 days. There was no clear treatment response identifiable on the MR scan of the brain following the third cycle and thus 4th–6th2 + cyclophosphamide 150 mg/m2 + dexamethasone 24 mg day 1–5 every 28 days. After the 6th cycle, MR showed partial regression of the brain lesions. PET-CT showed an increased accumulation of fluorodeoxyglucose in bone lesions. Second line treatment involved lenalidomide 25 mg/day days 1–21 every 28 days. Lenalidomide tolerance was excellent; the number of neutrophils and thrombocytes was within the physiological range throughout the treatment period. Follow-up MR showed complete remission of the brain lesions, while follow-up PET-CT showed further increase in fluorodeoxyglucose accumulation in the bones of lower limbs.
Conclusion:
Treatment with 2-chlorodeoxyadenosine-based regimen provided partial remission of Erdheim-Chester disease lesions in the brain, while treatment with lenalidomide resulted in complete remission of these lesions. Fluorodeoxyglucose continues to accumulate in the long bones of lower limbs. We are unable to elucidate the reasons for complete remission of the disease in the brain as per the MR and its progression in the long bones according to PET-CT. Further testing of lenalidomide in the treatment of this disease is required to support further use of this perspective treatment option.
Key words:
Erdheim-Chester disease – juvenile xanthogranuloma – osteosclerosis – skeletal scinigraphy – PET-CT – lenalidomide – 2-chlorodeoxyadenosine – cladribin – retroperitoneal fibrosis
This study was supported by the research programme of the Ministy of Health of the CR FUNDIN MZ0MOU2005 and prepeared as part of the Internal Grant Agency of the Czech Republic grants NT 12215-4, the Ministry of Education, Youth and Sports of the CR grants MSM0021622434, LC06027 and the Ministry of Health of the Czech Republic’s Internal Grant Agency grants IGA MZd NT11154, NT12130, NT12215 and NS10408.
The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study.
The Editorial Board declares that the manuscript met the ICMJE “uniform requirements” for biomedical papers.
Submitted:
14. 3. 2011
Accepted:
16. 5. 2011
Zdroje
1. Sverdlow SH, Campo E, Harris NL et al. WHO Classification of tumours of haematopoietic and lymphoid tissues. Lyon: IARC Press 2008.
2. Dickson BC, Pethe V, Chung CT et al. Systemic Erdheim--Chester disease. Virchows Arch 2008; 452(2): 221–227.
3. Lachenal F, Cotton F, Desmurs-Clavel H et al. Neurological manifestations and neuroradiological presentation of Erdheim-Chester disease: report of 6 cases and systematic review of the literature. J Neurol 2006; 253(10): 1267–1277.
4. Kinkor Z, Koudela K Jr, Koudela K et al. Warfarinem vyvolaná hemoragická pseudocysta malé pánve u ženy s vrozeným genetickým defektem koagulace komplikovaná usuračním pseudoxantomem pánevní kosti napodobujícím Erdheim-Chesterovu nemoc. Acta Chir Orthop Traum Čech 2007; 74(2): 114–117.
5. Kinkor Z. Severe pulmonary involvement in Erdheim-Chester disease (case report). Cesk Patol 2001; 37(3): 114–117.
6. Kinkror Z. Závažné plicní postižení u Erdheim-Chesterovy nemoci. Čs Patol 2001; 37/46(3): 114–117.
7. Kolář J, Kučera V, Povýšil C et al. Erdheim-Chester disease. Rofo 1984; 141(6): 698–701.
8. Mergancová J, Kubes L, Elleder M. Xanthogranulomatous processes in the area of the large vessels. Cesk Patol 1986; 22(3): 145–150.
9. Mergancová J, Kubeš L, Elleder M. A xanthogranulomatous process encircling large blood vessels (Erdheim--Chester disease). Czech Med 1988; 11(1): 57–64.
10. Kučera V, Čáp V, Kužel J et al. Vzácná příčina osteosklerózy: Erdheimův-Chesterův syndrom. ČS Radiol 1984; 38(6): 393–402.
11. Janková H, Říhová E. Juvenilní xanthogranulom. Oftalmologie 2007; 3: 214–218.
12. Vašáková M. Co je to Erdheimova nemoc? Kazuist Alergol Pneumol ORL 2006; 3(4): 22–25.
13. Mottl H, Koutecký J, Ganevová M. Strategie léčby histiocytózy z Langerhansových buněk u dětí. Čes-slov Pediat 1994; 49(2): 81.
14. Mottl H, Starý J. Histiocytóza z Langerhansových buněk u dětí – klinická diagnostika a současná léčba. Čes-slov Pediat 2007; 62(4): 200–225.
15. Plank L. Diagnostická patológia non-Langerhans cell histiocytóz. Vnitř Lék 2010; 56 (Suppl 2): 2S39–2S63.
16. Adam Z, Zahradová L, Krejčí M et al. Difuzní plošná normolipemická xantomatóza a nekrobiotický xantogranulom, asociované s monoklonální gamapatií – přínos PET-CT pro stanovení rozsahu nemoci a zkušenosti s léčbou. Popis dvou případů a přehled literatury. Vnitř Lék 2010; 56(11): 1158–1168.
17. Zahradová L, Adam Z, Feit J et al. Nekrobiotický xanthogranulom vzácná kožní komplikace u nemocného s mnohočetným myelomem. Vnitř Lék 2010; 56 (Suppl 2): 2S179–2S182.
18. Chester W. Über lipoigranulomatóse. Virchows Arch 1930; 279: 561–602.
19. Jaffe HL. Hematologic, degenerative and inflammatory disease of bones and joints. Philadelphia, PA: Lea and Febiger 1972: 531–541.
20. Miller RL, Sheeler LR, Bauer TW et al. Erdheim-Chester disease. Case report and review of the literature. Am J Med 1986; 80(5): 1230–1236.
21. Corradi D, Maestri R, Palmisano A et al. Idiopathic retroperitoneal fibrosis: clinicopathological features and diferencial diagnosis. Kidney Int 2007; 72(6): 742–753.
22. Alper MG, Zimmerman LE, Piana FG. Orbital manifestatiton of Erdheim-Chester disease. Trans Am Ophthalmol Soc 1983; 81: 64–85.
23. Garg T, Chander R, Gupta T et al. Erdheim-Chester disease with cutaneous features in an Indian patient. Skinmed 2008; 7(2): 103–106.
24. Kenn W, Eck M, Allolio B et al. Erdheim-Chester disease: evidence for a disease entity different from Langerhans cell histiocytosis? Three cases with detailed radiological and immonohistochemical analysis. Hum Pathol 2000; 31(6): 734–739.
25. Kenn W, Stäbler A, Zachoval R et al. Erdheim-Chester disease: a case report and literature overview. Eur Radiol 1999; 9(1): 153–158.
26. Veyssier-Belot C, Cacoub P, Caparros-Lefebvre D et al. Erdheim-Chester disease: clinical and radiologic characteristics of 59 cases. Medicine (Baltimore) 1996; 75(3): 157–169.
27. Perras B, Petersen D, Lorch H et al. Psychoneuroendocrine disturbances in a patient with a rare granulomatous disease. Exp Clin Endocrinol Diabetes 2002; 110(5): 248–252.
28. Brodkin CL, Wszolek ZK. Neurologic presentation of Erdheim-Chester disease. Neurol Neurochir Pol 2006; 40(5): 397–403.
29. De Abreu MR, Chung CB, Biswal S et al. Erdheim-Chester disease: MR imaging, anatomic, and histopathologic correlation of orbital involvement. AJNR Am J Neuroradiol 2004; 25(4): 627–630.
30. Salsano E, Savoiardo M, Nappini S et al. Late-onset sporadic ataxia, pontine lesion, and retroperitoneal fibrosis: a case of Erdheim-Chester disease. Neurol Sci 2008; 29(4): 263–267.
31. Sistermann R, Katthagen BD. Erdheim-Chester disease: a rare cause of knee and leg pain. Arch Orthop Trauma Surg 2000; 120(1–2): 112–113.
32. Yanagi T, Kato N, Yamane N et al. Verruca plana-like papules as a new manifestation of Erdheim-Chester disease. Arch Dermatol 2007; 143(7): 952–953.
33. Sivak-Callcott JA, Rootman J, Rasmussen SL et al. Adult xanthogranulomatous disease of the orbit and ocular adnexa: new immunohistochemical findings and clinical review. Br J Ophthalmol 2006; 90(5): 602–608.
34. Watermann DF, Kiesewetter F, Frosch PJ. Skin manifestations of Erdheim-Chester disease. Case report and review of the literature. Hautarzt 2001; 52(6): 510–517.
35. Hammond MD, Niemi EW, Ward TP et al. Adult orbital xanthogranuloma with associated adult-onset asthma. Ophthal Plast Reconstr Surg 2004; 20(4): 329–332.
36. Karcioglu ZA, Sharara N, Boles TL et al. Orbital xanthogranuloma: clinical and morphologic features in eight patients. Ophthal Plast Reconstr Surg 2003; 19(5): 372–381.
37. Kujat C, Martin J, Püschel W. Die Erdheim-Chester Krankheit. Radiologe 1991; 31: 297–306.
38. Fink MG, Levinson DJ, Brown NL et al. Erdheim-Chester disease. Case report with autopsy finding. Arch Pathol Lab Med 1991; 115(6): 619–623.
39. Tien RD, Brasch RC Jackson DE et al. Cerebral Erdheim--Chester disease: persistent enhancement with Gd-DTPA on MR images. Radiology 1989; 172(3): 791–792.
40. Martinez R. Erdheim-Chester disease: MR of intraaxilal and extraaxial brein stem lesion. AJNR Am J Neuroradiol 1995; 16(9): 1787–1790.
41. Ernemann U, Skalej M, Hermisson M et al. Primary cerebral non-Langerhans cell histiocytosis: MRI and differential diagnosis. Neuroradiology 2002; 44(9): 759–763.
42. Babu RR, Lansen TA, Chadburn A et al. Erdheim-Chester disease of the central nervous system. Report of two cases. J Neurosurg 1997; 86(5): 888–892.
43. Bohlega S, Alwatban J, Tulbah A et al. Cerebral manifestation of Erdheim-Chester disease: clinical and radiologic findings. Neurology 1997; 49(6): 1702–1705.
44. Weidauer S, von Stuckrad-Barre S, Dettmann E et al. Cerebral Erdheim-Chester disease: case report and review of the literature. Neuroradiology 2003; 45(4): 241–245.
45. Wright RA, Hermann RC, Parisi JE. Neurological manifestations of Erdheim-Chester disease. J Neurol Neurosurg Psychiatry 1999; 66(1): 72–75.
46. Shimada S, Ono K, Hashizume Y et al. Intracranial lesion of Erdheim-Chester disease. Hum Pathol 2007; 38(6): 950–951.
47. Grothe C, Urbach H, Bös M et al. Cerebellar syndrome, exophthalmos and secondary hypogonadism in Erdheim-Chester disease. Nervenarzt 2001; 72(6): 449–452.
48. Khamseh ME, Mollanai S, Hashemi F et al. Erdheim--Chester syndrome, presenting as hypogonadotropic hypogonadism and diabetes insipidus. J Endocrinol Invest 2002; 25(8): 727–729.
49. Kovacs K, Bilbao JM, Fornasier VL et al. Pituitary pathology in Erdheim-Chester disease. Endocr Pathol 2004; 15(2): 159–166.
50. Oweity T, Scheithauer BW, Ching HS et al. Multiple system Erdheim-Chester disease with massive hypothalamic-sellar involvement and hypopituitarism. J Neurosurg 2002; 96(2): 344–351.
51. Tritos NA, Weinrib S, Kaye TB. Endocrine manifestations of Erdheim-Chester disease (a distinct form of histiocytosis). J Intern Med 1998; 244(6): 529–535.
52. Sheu SY, Wenzel RR, Kersting R et al. Erdheim-Chester disease: a case report with multisystemic manifestation including testes, thyroid, and lymph nodes and a review of literature. J Clin Pathol 2004; 57(11): 1225–1228.
53. Bullmann C, Faust M, Hoffmann E et al. Five cases with central diabetes insipidus and hypogonadism as first presentation of neurosarcoidosis. Eur J Endocrinol 2000; 142(4): 365–372.
54. Mahnel R, Tan KH, Fahlbusch R et al. Problems in differential diagnosis of non Langerhans cell histiocytosis with pituitary involvement: case report and review of literature. Endocr Pathol 2002; 13(4): 361–368.
55. Sheen KC, Chang CC, Chang TC et al. Thikened pituitary stalk with central diabetes insipidus: report of 3 cases. J Formos Med Assoc 2001; 100(3): 198–204.
56. Takao T, Asaba K, Tanaka H et al. A case of of lymphocytic infundibuloneurohypophysitis schowing diabetes inspidus followed by anterior hypopituitarism associated with trombnasthenia. Endocr J 2000; 47(3): 285–291.
57. Tashiro T, Sano T, Xu B et al. Spectrum of different types of hypophysitis: a clinicopathologic study hypophysitis in 31 cases. Endocr Pathol 2002; 13(3): 183–185.
58. Mohn A, Fahlbusch R, Dörr HG. Panhypopituitarism associated with diabetes insipidus in a girl with a suprasellar arachnoid cyst. Horm Res 1999; 52(1): 35–38.
59. Folkerth RD, Price DL Jr, Schwartz M et al. Xanthomatous hypophysitis. Am J Surg Pathol 1998; 22(6): 736–741.
60. Athanasou NA, Barbatis C. Erdheim-Chester disease with epiphyseal and systemic disease. J Clin Pathol 1993; 46(5): 481–482.
61. Augoustides JG, Szeto WY. Unmasked diabetes insipidus after pericardial drainage and biopsy for pericardial effusion in association with Erdheim-Chester disease. J Thorac Cardiovasc Surg 2008; 136(1): 217–218.
62. Rushing EJ, Kaplan KJ, Mena H et al. Erdheim-Chester disease of the brain: cytological features and differential diagnosis of a challenging case. Diagn Cytopathol 2004; 31(6): 420–422.
63. Reithmeier T, Trost HA, Wolf S et al. Xanthogranuloma of the Erdheim-Chester type within the sellar region: case report. Clin Neuropathol 2002; 21(1): 24–28.
64. Allen TC, Chevez-Barrios P, Shetlar DJ et al. Pulmonary and ophthalmic involvement with Erdheim-Chester disease: a case report and review of the literature. Arch Pathol Lab Med 2004; 128(12): 1428–1431.
65. Kambouchner M, Colby TV, Demenge C et al. Erdheim-Chester disease with prominent pulmonary involvement associated with eosinophillic granuloma of mandibular bone. Histopathology 1997; 30(4): 353–358.
66. Krüger S, Krop C, Wibmer T et al. Erdheim-Chester disease: a rare cause of interstitial lung disease. Med Klin (Munich) 2006; 101(7): 573–576.
67. Protopapadakis C, Antoniou KM, Nicholson AG et al. Erdheim-Chester disease: pulmonary presentation in a case with advanced systemic involvement. Respiration 2009; 77(3): 337–340.
68. Shamburek RD, Brewer HB Jr, Gochuico BR. Erdheim--Chester disease: a rare multisystem histiocytic disorder associated with interstitial lung disease. Am J Med Sci 2001; 321(1): 66–75.
69. Rush WL, Andriko JA, Galateau-Salle F et al. Pulmonary pathology of Erdheim-Chester disease. Mod Pathol 2000; 13(7): 747–754.
70. Vašáková M, Fiala P, Kinkor Z. Erdheim-Chester disease: a case report. Monaldi Arch Chest Dis 2001; 56(2): 115–117.
71. Vaglio A, Corradi D, Maestri R et al. Pericarditis heralding Erdheim-Chester disease. Circulation 2008; 118(14): e511–e512.
72. Serratrice J, Granel B, De Roux C et al. “Coated aorta”: a new sign of Erdheim-Chester diseae. J Rheumatol 2000; 27(6): 1550–1553.
73. Haroche J, Amoura Z, Dion E et al. Cardiovascular involvement, an overlooked feature of Erdheim-Chester disease: report of 6 new cases and a literature review. Medicine (Baltimore) 2004; 83(6): 371–392.
74. Bassou D, El Kharras A, Taoufik AT et al. Cardiac Erdheim-Chester. Intern Med 2009; 48(1): 83–84.
75. Dion E, Graef C, Haroche J et al. Imaging of thoracoabdominal involvement in Erdheim-Chester disease. AJR Am J Roentgenol 2004; 183(5): 1253–1260.
76. Granier M, Micheau A, Serre I. A rare cause of cardiac tumour: an Erdheim-Chester disease with cardiac involvement co-existing with an intracerebral Langerhans cell histiocytosis. Eur Heart J 2008; 29(16): 1929–1935.
77. Loeffler AG, Memoli VA. Myocardial involvement in Erdheim-Chester disease. Arch Pathol Lab Med 2004; 128(6): 682–685.
78. Kudo Y, Iguchi N, Sumiyoshi T et al. Dramatic change of Ga-67 citrate uptake before and after corticosteroid therapy in a case of cardiac histiocytosis (Erdheim-Chester disease). J Nucl Cardiol 2006; 13(6): 867–869.
79. Loddenkemper K, Hoeyr B, Loddenkemper C et al. A case of Erdheim-Chester disease initially mistaken as Ormond’s diseae. Nat Clin Pract Rhematol 2008; 4(1): 50–55.
80. Bangard C, Lotz J, Rosenthal H et al. Erdheim-Chester disease versus multifocal fibrosis and Ormond’s disease: a diagnostic dilemma. Clin Radiol 2004; 59(12): 1136–1141.
81. Murray M, Marshall M, England E et al. Erdheim-Chester disease. Clin Radiol 2001; 56(6): 481–484.
82. Haroche J, Amoura Z, Touraine P et al. Bilateral adrenal infiltration in Erdheim-Chester disease. Report of seven cases and literature review. J Clin Endocrinol Metab 2007; 92(6): 2007–2012.
83. Pickhardt PJ, Bhalla S. Unusual nonneoplastic peritoneal and subperitoneal conditions: CT findings. Radiographics 2005; 25(3): 719–730.
84. Scheer M, Hon M, Fruauff AA et al. Perinephric xanthogranulomatosis: CT diagnosis and confirmation by CT-guided percutaneous biopsy. Clin Imaging 2000; 24(2): 64–67.
85. Surabhi VR, Menias C, Prasad SR et al. Neoplastic and non-neoplastic proliferative disorders of the perirenal space: cross-sectional imaging findings. Radiographics 2008; 28(4): 1005–1017.
86. Colin P, Ballereau C, Lambert M et al. Retroperitoneal infiltration as the first sign of Erdheim-Chester disease. Int J Urol 2008; 15(5): 455–456.
87. Moore FO, Berne JD, Fox AD. Mesenteric panniculitis and Erdheim-Chester disease: xanthogranulomatous diseases confused with malignancy. J Am Coll Surg 2007; 204(2): 326–327.
88. Droupy S, Attias, D, Eschwege P et al. Bilateral hydronefrosis in a patient with Erdheim-Chester disease. J Urol 1999; 162(6): 2084–2085.
89. O’Rourke R, Wong DC, Fleming S et al. Erdheim-Chester disease: a rare cause of acute renal failure. Australas Radiol 2007; 51: B48–B51.
90. Verdalles U, Goicoechea M, García de Vinuesa S et al. Erdheim-Chester disease: a rare cause of renal failure. Nephrol Dial Transplant 2007; 22(6): 1776–1777.
91. Wimpissinger TF, Schernthaner G, Feichtinger H et al. Compression of kidneys in Erdheim-Chester disease of retroperitoneum: open surgical approach. Urology 2005; 65(4): 798.
92. Gupta A, Aman K, Al-Babtain M et al. Multisystem Erdheim-Chester disease; a unique presentation with liver and axial skeletal involvement. Br J Haematol 2007; 138(3): 280.
93. Canbaz F, Dabak N, Baris S et al. Erdheim-Chester disease: 99mTc-MDP bone scan provides the diagnosis. Eur J Nucl Med Mol Imaging 2005; 32(8): 998.
94. Dion E, Graef C, Miquel A et al. Bone involvement in Erdheim-Chester disease: imaging findings including periostitis and partial epiphyseal involvement. Radiology 2006; 238(2): 632–639.
95. Girszyn N, Arnaud L, Villain D et al. Usefulness of combined positron emission tomography and computed tomography imaging in Erdheim-Chester disease. Rev Med Interne 2007; 28(11): 770–774.
96. Hoffmann EM, Müller-Forell W, Pitz S et al. Erdheim--Chester diseae: a case report. Graefes Arch Clin Exp Ophthalmol 2004; 242(9): 803–807.
97. Gottlieb R, Chen A. MR findings of Erdheim-Chester disease. J Comput Assist Tomogr 2002; 26(2): 257–261.
98. Nakahara T, Suzuki T, Uno K et al. 18F-FDG positron emission tomographic imaging in Erdheim-Chester disease with skeletal and extra-skeletal involvement. Leuk Lymphoma 2006; 47(5): 935–937.
99. Namwongprom S, Núñez R, Kim EE et al. Tc-99m MDP bone scintigraphy and positron emission tomography/computed tomography (PET/CT) imaging in Erdheim--Chester disease. Clin Nucl Med 2007; 32(1): 35–38.
100. Blum R, Seymour JF, Hicks RJ. Role of 18FDG-positron emission tomography scanning in the management of histiocytosis. Leuk Lymphoma 2002; 43(11): 2155–2157.
101. Palotás A, Bogáts G, Lázár M et al. Radiopharmaceutical diagnosis of Erdheim-Chester’s disease. Nucl Med Commun 2007; 28(1): 63–65.
102. Spyridonidis TJ, Giannakenas C, Barla P et al. Erdheim-Chester disease: a rare syndrome with a characteristic bone scintigraphy pattern. Ann Nucl Med 2008; 22(4): 323–326.
103. Zanglis A, Valsamaki P, Fountos G. Erdheim-Chester disease: symmetric uptake in the (99m)Tc-MDP bone scan. Hell J Nucl Med 2008; 11(3): 164–167.
104. Kim EE. Romero JA. Erdheim-Chester disease demonstrated with bone radiograph and scans. Clin Imaging 1997; 21(5): 328–331.
105. Koziolek MJ, Kunze E, Müller A et al. Erdheim-Chester disease. Dtsch Med Wochenschr 2005; 130(1–2): 25–28.
106. Arnaud L, Malek Z, Archambaud F et al. 18F-fluorodeoxyglucose-positron emission tomography scanning is more useful in followup than in the initial assessment of patients with Erdheim-Chester disease. Arthritis Rheum 2009; 60(10): 3128–3138.
107. Matsui K, Nagata Y, Hiraoka M. Radiotherapy for Erdheim-Chester disease. Int J Clin Oncol 2007; 12(3): 238–241.
108. Perlat A, Decaux O, Sébillot M et al. Erdheim-Chester disease with predominant mesenteric localization: lack of efficacy of interferon alpha. Joint Bone Spine 2009; 76(3): 315–317.
109. Vanichaniramol N, Kingpetch K, Buranasupkajorn P et al. Erdheim-Chester disease. Intern Med 2008; 47(18): 1633–1634.
110. Ono K, Oshiro M, Uemura K et al. Erdheim-Chester disease: case report with imunohistochemical and biochemical examination. Hum Pathol 1996; 27(1): 91–95.
111. Egan AJ, Boardman LA, Swensen SJ et al. Erdheim--Chester disease: clinical, radiologic and histopathologic findings in five patients with interstitial lung disease. Am J Surg Pathol 1999; 23(1): 17–26.
112. Kim NR, Ko YH, Choe YH et al. Erdheim-Chester disease with extensive marrow necrosis: a case report and literature review. Intern J Surg Pathol 2001; 9(1): 73–79.
113. Busemann C, Kallinich B, Schwesinger G et al. Erdheim-Chester disease with hemophagocytosis. Ann Hematol 2007; 86(11): 847–849.
114. Rao RN, Chang CC, Uysal N et al. Fulminant multisystem non-langerhans cell histiocytic proliferation with hemophagocytosis: a variant form of Erdheim-Chester disease. Arch Pathol Lab Med 2005; 129(2): e39–e43.
115. Lopez P, Estes ML. Immunohistochemical characterization of the histiocytes in sinus histiocytosis with massive lymphadenopathy: analysis of an extraosseal case. Hum Pathol 1989; 20(7): 711–715.
116. Bonetti F, Chilosi M, Menestrina F et al. Immunohistochemical analysis of Rosai-Dorfman histiocytosis. A disease of S-100 + CD1-histiocytes. Virchows Arch A Pathol Anat Histopathol 1987; 411(2): 129–135.
117. Foucar E, Rosai J, Dorfman R. Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity. Semin Diagn Pathol 1990; 7(1): 19–73.
118. Braiteh F, Boxrud C, Esmaeli B et al. Successful treatment of Erdheim-Chester disease, a non-Langerhans-cell histiocytosis, with interferon-alpha. Blood 2005; 106(9): 2992–2994.
119. Bourke SC, Nicholson AG, Gibson GJ. Erdheim-Chester disease: pulmonary infiltration responding to cyclophosphamide and prednisolone. Thorax 2003; 58(11): 1004–1005.
120. Haroche J, Amoura Z, Trad SG et al. Variability in the efficacy of interferon alpha in Erdheim-Chester disease by patient and site of involfement: results in eight patients. Arthritis Rheum 2006; 54(10): 3330–3336.
121. Esmaeli B, Ahmadi A, Tang R et al. Interferon therapy for orbital infiltration secondary to Erdheim-Chester disease. Am J Ophthalmol 2001; 132(6): 945–947.
122. Myra C, Sloper L, Tighe PJ et al. Treatment of Erdheim-Chester disease with cladribine: a rational approach. Br J Ophthalmol 2004; 88(6): 844–847.
123. Sheidow TG, Nicolle DA, Heathcote JG. Erdheim--Chester disease: two cases of orbital involvement. Eye (Lond) 2000; 14(4): 606–612.
124. Rajendra B, Duncan A, Parslew R et al. Successful treatment of central nervous system juvenila xanthogranulomatosis with cladribine. Pediatr Blood Cancer 2009; 52(3): 423–415.
125. Jendro MC, Zeidler H, Rosenthal H et al. Improvement of Erdheim-Chester disease in two patients by sequential treatment with vinblastine and mycophenolate mofetil. Clin Rheumatol 2004; 23(1): 52–56.
126. Mascalchi M, Nencini P, Nistri M et al. Failure of radiation therapy for brain involvement in Erdheim-Chester disease. J Neurooncol 2002; 59(2): 169–172.
127. Miller RC, Villà S, Kamer S et al. Palliative treatment of Erdheim-Chester disease with radiotherapy: a Rare Cancer Network study. Radiother Oncol 2006; 80(3): 323–326.
128. Haroche J, Amoura Z, Charlotte F et al. Imatinib mesylate for platelet-derived growth factor receptor-beta-positive Erdheim-Chester histiocytosis. Blood 2008; 111(11): 5413–5415.
129. Janku F, Amin HM, Yang D et al. Response of histiocytoses to imatinib mesylate: fire to ashes. J Clin Oncol 2010; 28(31): e633–e636.
130. Boissel N, Wechsler B, Leblond V. Treatment of refractory Erdheim-Chester disease with double autologous hematopoietic stem-cell transplantation. Ann Intern Med 2001; 135(9): 844–845.
131. Silapunt S, Chon SY. Generalized necrobiotic xanthogranuloma successfully treated with lenalidomide. J Drugs Dermatol 2010; 9(3): 273–276.
132. Aouba A, Georgin-Lavialle S, Pagnoux C et al. Rationale for efficacy of interleukin-1 targeting in Erdheim--Chester disease. Blood 2010; 116(20): 4070–4076.
133. Srikulmontree T, Massey HD, Roberts WN. Treatment of skeletal Erdheim-Chester disease with zoledronic acid: case report and proposed mechanisms of action. Rheumatol Int 2007; 27(3): 303–307.
134. Eyigör S, Kirazli Y, Memis A et al. Erdheim-Chester disease: the effect of bisphosphonate treatment – a case report. Arch Phys Med Rehabil 2005; 86(5): 1053–1057.
135. Mossetti G, Rendina D, Numis FG et al. Biochemical markers of bone turnover, serum levels of interleukin-6/interleukin-6 soluble receptor and bisphosphonate treatment in Erdheim-Chester disease. Clin Exp Rheumatol 2003; 21(2): 232–236.
136. Tan IB, Padhy AK, Thng CH et al. Intensely hypermetabolic extra-axial brainstem tumor in Erdheim-Chester disease. Clin Nucl Med 2009; 34(9): 604–607.
Štítky
Dětská onkologie Chirurgie všeobecná OnkologieČlánek vyšel v časopise
Klinická onkologie
2011 Číslo 5
- Metamizol jako analgetikum první volby: kdy, pro koho, jak a proč?
- Management pacientů s MPN a neobvyklou kombinací genových přestaveb – systematický přehled a kazuistiky
- Management péče o pacientku s karcinomem ovaria a neočekávanou mutací CDH1 – kazuistika
- Neodolpasse je bezpečný přípravek v krátkodobé léčbě bolesti
- Cinitaprid – v Česku nová účinná látka nejen pro léčbu dysmotilitní dyspepsie
Nejčtenější v tomto čísle
- Parciální regrese ložisek Erdheimovy-Chesterovy nemoci v CNS po léčbě 2-chlorodeoxyadenosinem a jejich kompletní vymizení při léčbě lenalidomidem
- Neuroendoskopická biopsie tumoru mozku
- Sekundární angiosarkomy po konzervativní léčbě nádorů prsu
- Onkochirurg doc. MUDr. Zdeněk Pačovský, CSc., zemřel